Unexpected photo-induced oxidative cyclization and luminescence switching in molecular aggregates of two acylhydrazone-based Ir(iii) complexes†

IF 6.4 1区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR Inorganic Chemistry Frontiers Pub Date : 2025-03-31 DOI:10.1039/D5QI00527B
Xin-Tong Lv, Xiao-Dong Liu, Zhiping Zhou and Deng-Ke Cao
{"title":"Unexpected photo-induced oxidative cyclization and luminescence switching in molecular aggregates of two acylhydrazone-based Ir(iii) complexes†","authors":"Xin-Tong Lv, Xiao-Dong Liu, Zhiping Zhou and Deng-Ke Cao","doi":"10.1039/D5QI00527B","DOIUrl":null,"url":null,"abstract":"<p >Two iridium complexes, namely [Ir(ppy)<small><sub>2</sub></small>(mbpymbh)]PF<small><sub>6</sub></small> (<strong>1</strong>) and [Ir(dfppy)<small><sub>2</sub></small>(mbpymbh)]PF<small><sub>6</sub></small> (<strong>2</strong>), exhibit unexpected photoreactivity, although the incorporated ligands ppyH, dfppyH and mbpymbh have no inherent photochemical activity. The molecular aggregates of <strong>1</strong> and <strong>2</strong>, formed in a CH<small><sub>3</sub></small>CN–H<small><sub>2</sub></small>O (v/v = 1/9) mixed solvent, show photo-induced luminescence switching, with the emission-color change from red to orange for <strong>1</strong>, while a transition from the off state to on state with an emission band at 566 nm for <strong>2</strong>. These changes in luminescence are assigned to photo-induced oxidative cyclization of the acylhydrazone units in <strong>1</strong> and <strong>2</strong>, thus generating photoproducts <strong>1-O</strong> and <strong>2-O</strong>. Complexes <strong>1-O</strong> and <strong>2-O</strong> were isolated and identified from their crystal structures. We discussed both the effect factors and the reaction mechanism of the photo-oxidation reactions for complexes <strong>1</strong> and <strong>2</strong>, as well as the luminescence properties of complexes <strong>1</strong>, <strong>2</strong>, <strong>1-O</strong> and <strong>2-O</strong>. The discovery of photo-induced oxidative cyclization in this work not only provides a new class of photo-responsive luminescent materials, but also offers a novel synthesis method for 1,3,4-oxadiazole-based Ir(<small>III</small>) complexes.</p>","PeriodicalId":79,"journal":{"name":"Inorganic Chemistry Frontiers","volume":" 11","pages":" 3940-3948"},"PeriodicalIF":6.4000,"publicationDate":"2025-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganic Chemistry Frontiers","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/qi/d5qi00527b","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0

Abstract

Two iridium complexes, namely [Ir(ppy)2(mbpymbh)]PF6 (1) and [Ir(dfppy)2(mbpymbh)]PF6 (2), exhibit unexpected photoreactivity, although the incorporated ligands ppyH, dfppyH and mbpymbh have no inherent photochemical activity. The molecular aggregates of 1 and 2, formed in a CH3CN–H2O (v/v = 1/9) mixed solvent, show photo-induced luminescence switching, with the emission-color change from red to orange for 1, while a transition from the off state to on state with an emission band at 566 nm for 2. These changes in luminescence are assigned to photo-induced oxidative cyclization of the acylhydrazone units in 1 and 2, thus generating photoproducts 1-O and 2-O. Complexes 1-O and 2-O were isolated and identified from their crystal structures. We discussed both the effect factors and the reaction mechanism of the photo-oxidation reactions for complexes 1 and 2, as well as the luminescence properties of complexes 1, 2, 1-O and 2-O. The discovery of photo-induced oxidative cyclization in this work not only provides a new class of photo-responsive luminescent materials, but also offers a novel synthesis method for 1,3,4-oxadiazole-based Ir(III) complexes.

Abstract Image

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
两个酰基腙基Ir(III)配合物分子聚集体中意想不到的光诱导氧化环化和发光开关
两个铱配合物,即[Ir(ppy)2(mbpymbh)]PF6(1)和[Ir(dfppy)2(mbpymbh)]PF6(2),表现出意想不到的光反应性,尽管结合的配体ppyH, dfppyH和mbpymbh没有固有的光化学活性。在CH3CN-H2O (v/v = 1/9)混合溶剂中形成的1和2的分子聚集体表现出光致发光开关,其中1的发光颜色由红色变为橙色,而2的发光带在566 nm处由关闭状态转变为打开状态。这些发光变化归因于1和2中的酰基腙单元的光诱导氧化环化,从而产生光产物1- o和2- o。从配合物1-O和2-O的晶体结构上进行了分离和鉴定。讨论了配合物1和2的光氧化反应的影响因素和反应机理,以及配合物1、2、1- o和2- o的发光性质。本研究中光诱导氧化环化的发现不仅提供了一类新的光响应发光材料,而且为1,3,4-恶二唑基Ir(III)配合物的合成提供了一种新的方法。
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
Inorganic Chemistry Frontiers
Inorganic Chemistry Frontiers CHEMISTRY, INORGANIC & NUCLEAR-
CiteScore
10.40
自引率
7.10%
发文量
587
审稿时长
1.2 months
期刊介绍: The international, high quality journal for interdisciplinary research between inorganic chemistry and related subjects
期刊最新文献
Ultra-efficient energy transfer and near-infrared luminescence in hexagonal aluminate phosphors enabled by heterogeneous ion pairs co-doping Truss bridge-like anhydrous stacking in hybrid crystal triggers ultra-high stability and robust birefringence Bridging the gap: thymine segments to create single-strand versions of DNA2-[Ag₁₆Cl₂]8+ A low-loss optical waveguide from a 1D europium nanocluster Exciplex-based multi-stimuli-responsive luminescent materials: photo-recoverable mechanochromic luminescence for reusable paper 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