Circularly Polarized Room Temperature Red Phosphorescence from a [9]-Heterohelicene Diimide

Sankar, Jeyaraman, Shivangee, Jha, Kundan Singh, Mehra, Pradip Kumar, Mondal, Camelia, Dutta, Jatish, Kumar, Sentamizh Selven, Ramalingam
{"title":"Circularly Polarized Room Temperature Red Phosphorescence from a [9]-Heterohelicene Diimide","authors":"Sankar, Jeyaraman, Shivangee, Jha, Kundan Singh, Mehra, Pradip Kumar, Mondal, Camelia, Dutta, Jatish, Kumar, Sentamizh Selven, Ramalingam","doi":"10.26434/chemrxiv-2024-44vd8","DOIUrl":null,"url":null,"abstract":"Circularly polarized room temperature phosphorescence (CP-RTP) in the red region is fascinating, however, challenging to achieve in organic molecules. The difficulty stems from two necessary conditions required to design such molecules. Firstly, achieving circularly polarized luminescence, with higher emission quantum yield in the longer wavelength region is challeng-ing. Secondly, attaining phosphorescence from such molecules under ambient conditions is difficult. Achieving both the cri-teria together in a single molecule is ambitious. In this work, we devise a novel design strategy to realize CP-RTP from a [9]-heterohelicene diimide. The designed molecule possesses helical chirality and an extended conjugation affording chiroptical responses in the red region. Interestingly a four-fold increment in the dissymmetry factor has been achieved by switching the solvent polarity. Furthermore, the incorporation of sulphur atom in the molecular framework facilitates a prolonged emis-sion lifetime of 1.09 ms under ambient conditions, making it the only example of a rylene diimide exhibiting CP-RTP.","PeriodicalId":9813,"journal":{"name":"ChemRxiv","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemRxiv","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.26434/chemrxiv-2024-44vd8","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Circularly polarized room temperature phosphorescence (CP-RTP) in the red region is fascinating, however, challenging to achieve in organic molecules. The difficulty stems from two necessary conditions required to design such molecules. Firstly, achieving circularly polarized luminescence, with higher emission quantum yield in the longer wavelength region is challeng-ing. Secondly, attaining phosphorescence from such molecules under ambient conditions is difficult. Achieving both the cri-teria together in a single molecule is ambitious. In this work, we devise a novel design strategy to realize CP-RTP from a [9]-heterohelicene diimide. The designed molecule possesses helical chirality and an extended conjugation affording chiroptical responses in the red region. Interestingly a four-fold increment in the dissymmetry factor has been achieved by switching the solvent polarity. Furthermore, the incorporation of sulphur atom in the molecular framework facilitates a prolonged emis-sion lifetime of 1.09 ms under ambient conditions, making it the only example of a rylene diimide exhibiting CP-RTP.
来自 [9]- 杂己烯二亚胺的环形极化室温红色磷光
红色区域的圆偏振室温磷光(CP-RTP)令人着迷,但要在有机分子中实现却极具挑战性。困难源于设计此类分子所需的两个必要条件。首先,在较长的波长区域实现具有较高发射量子产率的圆偏振发光具有挑战性。其次,在环境条件下从此类分子中获得磷光也很困难。要在单个分子中同时实现这两个目标,难度很大。在这项工作中,我们设计了一种新颖的设计策略,利用[9]-己烯二亚胺实现了 CP-RTP。所设计的分子具有螺旋手性和扩展共轭,可在红色区域产生千色响应。有趣的是,通过改变溶剂极性,不对称因子增加了四倍。此外,由于在分子框架中加入了硫原子,因此在环境条件下的发射寿命延长至 1.09 毫秒,这也是唯一一个表现出 CP-RTP 的亚烯烃二亚胺实例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信