Conformational regulation to realize modifiable ESIPT (excited-state intramolecular proton transfer) through intermolecular interactions†

IF 6.4 2区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Materials Chemistry Frontiers Pub Date : 2025-02-15 DOI:10.1039/D5QM00012B
Shao-Zhe Yi, Bao-Ning Li, Wen He and Mei Pan
{"title":"Conformational regulation to realize modifiable ESIPT (excited-state intramolecular proton transfer) through intermolecular interactions†","authors":"Shao-Zhe Yi, Bao-Ning Li, Wen He and Mei Pan","doi":"10.1039/D5QM00012B","DOIUrl":null,"url":null,"abstract":"<p >Regulating molecular conformation changes is crucial yet challenging for manipulating multiple-responsive emissions in excited-state intramolecular proton transfer (ESIPT) materials. In this work, we explored the specific emission regulation of a dual-ESIPT-active molecule, BDIBD (2,5-bis(4,5-diphenyl-1<em>H</em>-imidazol-2-yl)benzene-1,4-diol), by subtly controlling the ground and excited states through different crystallization conformations. Notably, the crystals obtained in dimethylformamide (BDIBD–DMF) and methanol (BDIBD–MeOH) exhibited a single emission band, corresponding to the green and red emission from the keto<small><sup>1st</sup></small> and keto<small><sup>2nd</sup></small> excited states, respectively, while the crystals obtained in acetone (BDIBD–ACE) displayed dual emissions from both states, resulting in an overall yellow color. A comprehensive theoretical study verified that the modified intermolecular interactions, due to different crystallization conformations, regulated emissions by affecting the energy barrier of dual-ESIPT processes. The above results provide a concrete understanding of the regulation of excited-state emissions through ground-state conformational changes in ESIPT processes, as well as unique insights into the design and application of novel ESIPT emission materials.</p>","PeriodicalId":86,"journal":{"name":"Materials Chemistry Frontiers","volume":" 7","pages":" 1181-1188"},"PeriodicalIF":6.4000,"publicationDate":"2025-02-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/qm/d5qm00012b?page=search","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Materials Chemistry Frontiers","FirstCategoryId":"88","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/qm/d5qm00012b","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

Regulating molecular conformation changes is crucial yet challenging for manipulating multiple-responsive emissions in excited-state intramolecular proton transfer (ESIPT) materials. In this work, we explored the specific emission regulation of a dual-ESIPT-active molecule, BDIBD (2,5-bis(4,5-diphenyl-1H-imidazol-2-yl)benzene-1,4-diol), by subtly controlling the ground and excited states through different crystallization conformations. Notably, the crystals obtained in dimethylformamide (BDIBD–DMF) and methanol (BDIBD–MeOH) exhibited a single emission band, corresponding to the green and red emission from the keto1st and keto2nd excited states, respectively, while the crystals obtained in acetone (BDIBD–ACE) displayed dual emissions from both states, resulting in an overall yellow color. A comprehensive theoretical study verified that the modified intermolecular interactions, due to different crystallization conformations, regulated emissions by affecting the energy barrier of dual-ESIPT processes. The above results provide a concrete understanding of the regulation of excited-state emissions through ground-state conformational changes in ESIPT processes, as well as unique insights into the design and application of novel ESIPT emission materials.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
通过分子间相互作用实现可改变的激发态分子内质子转移的构象调控
调控分子构象变化对于控制激发态分子内质子转移(ESIPT)材料的多响应发射至关重要,但也具有挑战性。在这项工作中,我们探索了双esipt活性分子BDIBD(2,5-双(4,5-二苯基- 1h -咪唑-2-基)苯-1,4-二醇)通过不同的结晶构象微妙地控制基态和激发态的特定发射调控。值得注意的是,在二甲基甲酰胺(BDIBD-DMF)和甲醇(BDIBD-MeOH)中得到的晶体表现出单一的发射带,分别对应于酮1和酮2激发态的绿色和红色发射,而在丙酮(BDIBD-ACE)中得到的晶体表现出两种状态的双发射,导致整体颜色为黄色。一项全面的理论研究证实,由于不同的结晶构象,分子间相互作用的改变通过影响双esipt过程的能量势垒来调节发射。上述结果为ESIPT过程中基态构象变化对激发态发射的调控提供了具体的认识,也为新型ESIPT发射材料的设计和应用提供了独特的见解。
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 去求助
来源期刊
Materials Chemistry Frontiers
Materials Chemistry Frontiers Materials Science-Materials Chemistry
CiteScore
12.00
自引率
2.90%
发文量
313
期刊介绍: Materials Chemistry Frontiers focuses on the synthesis and chemistry of exciting new materials, and the development of improved fabrication techniques. Characterisation and fundamental studies that are of broad appeal are also welcome. This is the ideal home for studies of a significant nature that further the development of organic, inorganic, composite and nano-materials.
期刊最新文献
Electrochemical QCM-D for insights into organic mixed ionic–electronic conductors and transistors (OECTs) Photoresponsive multifunctional anisotropic conductive hydrogel membrane for human motion detection, information encryption and transmission A hydrogen bonding strategy to strengthen room temperature phosphorescence of nitrogen-modified benzocarbazole Morphology, interface, and energy field engineering of ternary oxide photoanodes for efficient photoelectrochemical water splitting Recent advances in room-temperature phosphorescence metal–organic frameworks: structural design, property modulation, and emerging applications
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1