{"title":"亚磺酰亚胺：融合噻吩环的无穷亚胺。","authors":"Peter B. Karadakov , Edward Cummings","doi":"10.1039/d4cc05179c","DOIUrl":null,"url":null,"abstract":"<div><div>Sulfinfinitenes, analogues of infinitene constructed from thiophene rings and assembled by applying a “cut–twist–restitch” sequence to two sulflowers, are explored through DFT calculations. The sulfinfinitene with 16 thiophene rings is only slightly more strained than the [8]sulflower, which has been synthesized, and can be considered as a promising synthetic target.</div></div>","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":"60 98","pages":"Pages 14633-14636"},"PeriodicalIF":4.2000,"publicationDate":"2024-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/cc/d4cc05179c?page=search","citationCount":"0","resultStr":"{\"title\":\"Sulfinfinitenes: infinitenes of fused thiophene rings†\",\"authors\":\"Peter B. Karadakov , Edward Cummings\",\"doi\":\"10.1039/d4cc05179c\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Sulfinfinitenes, analogues of infinitene constructed from thiophene rings and assembled by applying a “cut–twist–restitch” sequence to two sulflowers, are explored through DFT calculations. The sulfinfinitene with 16 thiophene rings is only slightly more strained than the [8]sulflower, which has been synthesized, and can be considered as a promising synthetic target.</div></div>\",\"PeriodicalId\":67,\"journal\":{\"name\":\"Chemical Communications\",\"volume\":\"60 98\",\"pages\":\"Pages 14633-14636\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2024-11-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.rsc.org/en/content/articlepdf/2024/cc/d4cc05179c?page=search\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Communications\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S1359734524024029\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/11/13 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Communications","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1359734524024029","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/13 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Sulfinfinitenes: infinitenes of fused thiophene rings†
Sulfinfinitenes, analogues of infinitene constructed from thiophene rings and assembled by applying a “cut–twist–restitch” sequence to two sulflowers, are explored through DFT calculations. The sulfinfinitene with 16 thiophene rings is only slightly more strained than the [8]sulflower, which has been synthesized, and can be considered as a promising synthetic target.
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