全面优化:中心芳基推挽四烯色团和用于电光学的客座聚合物。

IF 3 4区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Di Zhang, Jingdong Luo
{"title":"全面优化:中心芳基推挽四烯色团和用于电光学的客座聚合物。","authors":"Di Zhang, Jingdong Luo","doi":"10.1002/cplu.202400551","DOIUrl":null,"url":null,"abstract":"<p><p>The research and development of push-pull tetraene chromophores (PPT-phores) have contributed greatly to the field of organic electro-optic (EO) materials and devices since the inauguration of CLD-1 in 2001. This study is thus a systematic contribution to synthesize and characterize a series of centro-arylated PPT-phores based on strong electron-donating tetrahydroquinolinyl groups and variable strong electron-accepting tricyanofuran derivatives. In particular, we report the crystallographic data to show various packing modes of these PPT-phores with detailed information about bond length alternation and intermolecular interactions, the optical absorption edges of guest-host polymers by the Tauc model, and the anisotropy and dispersion of Pockels tensors for the poled polymers by attenuated total reflection spectroscopy. Such analyses have not been addressed to any significant extent previously and are fundamentally important to the future development of PPT-phore-based EO materials and devices. The poled films of several centro-arylated PPT-phores in polycarbonates exhibited large EO activities, excellent thermal stability, and tunable optical transparency at the telecom O- and C-band. The study demonstrates the effectiveness of π-bridge centro-arylation enabled by molecular shape modification and rigidity enhancement, over the relatively flexible and labile thioether or alkoxy groups, in rational design of hyperpolarizable PPT-phores for high-performance EO polymers.</p>","PeriodicalId":148,"journal":{"name":"ChemPlusChem","volume":" ","pages":"e202400551"},"PeriodicalIF":3.0000,"publicationDate":"2024-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Optimization across-the-Board: Centro-Arylated Push-Pull Tetraene Chromophores and Guest-Host Polymers for Electro-Optics.\",\"authors\":\"Di Zhang, Jingdong Luo\",\"doi\":\"10.1002/cplu.202400551\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The research and development of push-pull tetraene chromophores (PPT-phores) have contributed greatly to the field of organic electro-optic (EO) materials and devices since the inauguration of CLD-1 in 2001. This study is thus a systematic contribution to synthesize and characterize a series of centro-arylated PPT-phores based on strong electron-donating tetrahydroquinolinyl groups and variable strong electron-accepting tricyanofuran derivatives. In particular, we report the crystallographic data to show various packing modes of these PPT-phores with detailed information about bond length alternation and intermolecular interactions, the optical absorption edges of guest-host polymers by the Tauc model, and the anisotropy and dispersion of Pockels tensors for the poled polymers by attenuated total reflection spectroscopy. Such analyses have not been addressed to any significant extent previously and are fundamentally important to the future development of PPT-phore-based EO materials and devices. The poled films of several centro-arylated PPT-phores in polycarbonates exhibited large EO activities, excellent thermal stability, and tunable optical transparency at the telecom O- and C-band. The study demonstrates the effectiveness of π-bridge centro-arylation enabled by molecular shape modification and rigidity enhancement, over the relatively flexible and labile thioether or alkoxy groups, in rational design of hyperpolarizable PPT-phores for high-performance EO polymers.</p>\",\"PeriodicalId\":148,\"journal\":{\"name\":\"ChemPlusChem\",\"volume\":\" \",\"pages\":\"e202400551\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2024-11-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ChemPlusChem\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1002/cplu.202400551\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemPlusChem","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/cplu.202400551","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

自 2001 年 CLD-1 诞生以来,推拉四烯发色团(PPT-phores)的研究和开发为有机电光材料和器件领域做出了巨大贡献。因此,本研究系统地合成并表征了一系列基于强电子供体四氢喹啉基团和可变强电子受体三氰呋喃衍生物的向心芳基化 PPT 荧光团。我们特别报告了晶体学数据,这些数据显示了这些 PPT-phores 的各种堆积模式,并提供了有关键长交替和分子间相互作用的详细信息;通过陶氏模型分析了客主聚合物的光学吸收边缘;通过衰减全反射光谱分析了极化聚合物的各向异性和波克尔斯张量的分散性。这些分析以前从未在很大程度上进行过,对基于 PPT-phore 的环氧乙烷材料和设备的未来发展至关重要。聚碳酸酯中几种向心芳基化的 PPT-phore极化膜表现出很高的环氧乙烷活性、出色的热稳定性以及在电信 O 波段和 C 波段的可调光学透明度。这项研究表明,π桥向心芳基化通过分子形状修饰和刚性增强,比相对灵活易变的硫醚或烷氧基更有效,可用于高性能环氧乙烷聚合物的超极化 PPT-phores 的合理设计。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Optimization across-the-Board: Centro-Arylated Push-Pull Tetraene Chromophores and Guest-Host Polymers for Electro-Optics.

The research and development of push-pull tetraene chromophores (PPT-phores) have contributed greatly to the field of organic electro-optic (EO) materials and devices since the inauguration of CLD-1 in 2001. This study is thus a systematic contribution to synthesize and characterize a series of centro-arylated PPT-phores based on strong electron-donating tetrahydroquinolinyl groups and variable strong electron-accepting tricyanofuran derivatives. In particular, we report the crystallographic data to show various packing modes of these PPT-phores with detailed information about bond length alternation and intermolecular interactions, the optical absorption edges of guest-host polymers by the Tauc model, and the anisotropy and dispersion of Pockels tensors for the poled polymers by attenuated total reflection spectroscopy. Such analyses have not been addressed to any significant extent previously and are fundamentally important to the future development of PPT-phore-based EO materials and devices. The poled films of several centro-arylated PPT-phores in polycarbonates exhibited large EO activities, excellent thermal stability, and tunable optical transparency at the telecom O- and C-band. The study demonstrates the effectiveness of π-bridge centro-arylation enabled by molecular shape modification and rigidity enhancement, over the relatively flexible and labile thioether or alkoxy groups, in rational design of hyperpolarizable PPT-phores for high-performance EO polymers.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
ChemPlusChem
ChemPlusChem CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
5.90
自引率
0.00%
发文量
200
审稿时长
1 months
期刊介绍: ChemPlusChem is a peer-reviewed, general chemistry journal that brings readers the very best in multidisciplinary research centering on chemistry. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies. Fully comprehensive in its scope, ChemPlusChem publishes articles covering new results from at least two different aspects (subfields) of chemistry or one of chemistry and one of another scientific discipline (one chemistry topic plus another one, hence the title ChemPlusChem). All suitable submissions undergo balanced peer review by experts in the field to ensure the highest quality, originality, relevance, significance, and validity.
×
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