{"title":"通过烁尔反应合成基于苝的扭转发射型弯曲纳米石墨烯","authors":"Siddhartha Samanta, Sahina Khatun, Sanhita Maity, Anirban Pradhan","doi":"10.1002/ejoc.202401170","DOIUrl":null,"url":null,"abstract":"A twisted chiral nanographene (NG) surrounded by eight bulky tert-butyl groups fused with emissive chromophore perylene was synthesized by highly regioselective cyclodehydrogenation strategy in which a double [6]helicene was formed simultaneously. The twisted 4-meso was unambiguously confirmed by single crystal X-ray analysis. The NG showed an excellent photoluminescence quantum yield (φf) of 55%, indicating its great potential for chiral optoelectronics.","PeriodicalId":167,"journal":{"name":"European Journal of Organic Chemistry","volume":"1 1","pages":""},"PeriodicalIF":2.5000,"publicationDate":"2024-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Perylene Based Twisted Emissive Curved Nanographene Synthesis through Scholl Reaction\",\"authors\":\"Siddhartha Samanta, Sahina Khatun, Sanhita Maity, Anirban Pradhan\",\"doi\":\"10.1002/ejoc.202401170\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A twisted chiral nanographene (NG) surrounded by eight bulky tert-butyl groups fused with emissive chromophore perylene was synthesized by highly regioselective cyclodehydrogenation strategy in which a double [6]helicene was formed simultaneously. The twisted 4-meso was unambiguously confirmed by single crystal X-ray analysis. The NG showed an excellent photoluminescence quantum yield (φf) of 55%, indicating its great potential for chiral optoelectronics.\",\"PeriodicalId\":167,\"journal\":{\"name\":\"European Journal of Organic Chemistry\",\"volume\":\"1 1\",\"pages\":\"\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2024-10-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"European Journal of Organic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1002/ejoc.202401170\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Organic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/ejoc.202401170","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0
摘要
通过高区域选择性环化氢化策略合成了一种由八个笨重的叔丁基环绕的扭曲手性纳米石墨烯(NG),并与发射性发色团苝融合,同时形成了双 [6] 螺旋烯。通过单晶 X 射线分析,明确地确认了扭曲的 4-meso。该 NG 的光致发光量子产率 (φf) 高达 55%,显示了其在手性光电子学方面的巨大潜力。
Perylene Based Twisted Emissive Curved Nanographene Synthesis through Scholl Reaction
A twisted chiral nanographene (NG) surrounded by eight bulky tert-butyl groups fused with emissive chromophore perylene was synthesized by highly regioselective cyclodehydrogenation strategy in which a double [6]helicene was formed simultaneously. The twisted 4-meso was unambiguously confirmed by single crystal X-ray analysis. The NG showed an excellent photoluminescence quantum yield (φf) of 55%, indicating its great potential for chiral optoelectronics.
期刊介绍:
The European Journal of Organic Chemistry (2019 ISI Impact Factor 2.889) publishes Full Papers, Communications, and Minireviews from the entire spectrum of synthetic organic, bioorganic and physical-organic chemistry. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies.
The following journals have been merged to form two leading journals, the European Journal of Organic Chemistry and the European Journal of Inorganic Chemistry:
Liebigs Annalen
Bulletin des Sociétés Chimiques Belges
Bulletin de la Société Chimique de France
Gazzetta Chimica Italiana
Recueil des Travaux Chimiques des Pays-Bas
Anales de Química
Chimika Chronika
Revista Portuguesa de Química
ACH—Models in Chemistry
Polish Journal of Chemistry.