Nonlinear Optical Chromophores Containing Fused Terthiophene As A New Type of Electron Relay

O. Kim, A. Fort, M. Barzoukas, J. Lehn
{"title":"Nonlinear Optical Chromophores Containing Fused Terthiophene As A New Type of Electron Relay","authors":"O. Kim, A. Fort, M. Barzoukas, J. Lehn","doi":"10.1364/otfa.1997.fa.3","DOIUrl":null,"url":null,"abstract":"Thiophene-based D-A molecules have been actively sought recently, exploiting interesting results indicating that the incorporation of a thiophene unit or the replacement of a phenylene moiety by thienylene in the relay of a D-A molecule enhanced the molecular hyperpolarizability (μβ(0)) significantly (1-3). Accordingly, it is expected that oligothiophenes give a larger contribution to the μβ(0) compared to oligophenylenes. As in the case of polyenes, the rigidification of thiophenes (by cyclization) has also been known to enhance charge-transfer in push-pull D-A molecules, as indicated by a bathochromic shift of absorption bands and a stronger solvatochromism compared to the flexible counterpart (4,5). A further indication for the effectiveness of fused thiophenes as relay is demonstrated by the fact that their absorption maxima increase linearly with the number of rings up to five (6). Aside from the electronic features, another merit of thiophenes is their inherent thermal stability from which thiophene-containing chromophores will benefit (2,3).","PeriodicalId":378320,"journal":{"name":"Organic Thin Films for Photonics Applications","volume":"3 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic Thin Films for Photonics Applications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1364/otfa.1997.fa.3","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

Thiophene-based D-A molecules have been actively sought recently, exploiting interesting results indicating that the incorporation of a thiophene unit or the replacement of a phenylene moiety by thienylene in the relay of a D-A molecule enhanced the molecular hyperpolarizability (μβ(0)) significantly (1-3). Accordingly, it is expected that oligothiophenes give a larger contribution to the μβ(0) compared to oligophenylenes. As in the case of polyenes, the rigidification of thiophenes (by cyclization) has also been known to enhance charge-transfer in push-pull D-A molecules, as indicated by a bathochromic shift of absorption bands and a stronger solvatochromism compared to the flexible counterpart (4,5). A further indication for the effectiveness of fused thiophenes as relay is demonstrated by the fact that their absorption maxima increase linearly with the number of rings up to five (6). Aside from the electronic features, another merit of thiophenes is their inherent thermal stability from which thiophene-containing chromophores will benefit (2,3).
含熔融噻吩的非线性光学发色团作为一种新型电子继电器
噻吩基的D-A分子最近得到了积极的研究,发现在D-A分子的继电反应中加入噻吩单元或用噻炔取代苯基片段可显著提高分子的超极化率(μβ(0))(1-3)。因此,与低聚噻吩相比,低聚噻吩对μβ(0)的贡献更大。与多烯的情况一样,噻吩的刚性(通过环化)也被认为可以增强推挽式D-A分子中的电荷转移,这可以通过吸收带的深变色移动和与柔性对应物相比更强的溶剂变色来表明(4,5)。熔合噻吩作为继电器的有效性进一步表明,它们的吸收最大值随着环数的增加而线性增加(6)。除了电子特性外,噻吩的另一个优点是其固有的热稳定性,这将使含噻吩的发色团受益(2,3)。
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:604180095
Book学术官方微信