Cyclometalated Iridium(III) Complex with Substituted Benzimidazole: pH Directed Organelle‐specific Localization within Lysosome

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Subhra Sil, Afaq Hussain, Jayasri Das Sarma, Parna Gupta
{"title":"Cyclometalated Iridium(III) Complex with Substituted Benzimidazole: pH Directed Organelle‐specific Localization within Lysosome","authors":"Subhra Sil, Afaq Hussain, Jayasri Das Sarma, Parna Gupta","doi":"10.1002/cbic.202400597","DOIUrl":null,"url":null,"abstract":"We report the synthesis and pH dependent emission spectral behaviour of four emissive iridium(III) complexes (Ir1 – Ir4) with two isomeric pairs of bis‐trifluoromethyl appended benzimidazole ligands. The imidazolyl hydrogen(N‐H) has been replaced by phenyl groups (N‐Ph) in two ligands to understand the impact of hydrogen bonding on the photophysical properties of the complexes and it indeed plays interesting role in the charge‐transfer dynamics. The pH dependent electronic spectral change is observed for two of the complexes. The enhancement of emission intensity is observed at different wavelength for pH < 7 and pH > 7 for Ir1 and Ir3. The emission sensing of biogenic amines with pka values ranging from 5.80 – 9.74 is reported along with cellular imaging. The complex Ir1 specifically localizes within lysosome (pH = 4.5 – 5) and thus image this organelle with great precision. The detail electronic spectra and electrochemical behaviour were reported here along with TDDFT results.","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1002/cbic.202400597","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0

Abstract

We report the synthesis and pH dependent emission spectral behaviour of four emissive iridium(III) complexes (Ir1 – Ir4) with two isomeric pairs of bis‐trifluoromethyl appended benzimidazole ligands. The imidazolyl hydrogen(N‐H) has been replaced by phenyl groups (N‐Ph) in two ligands to understand the impact of hydrogen bonding on the photophysical properties of the complexes and it indeed plays interesting role in the charge‐transfer dynamics. The pH dependent electronic spectral change is observed for two of the complexes. The enhancement of emission intensity is observed at different wavelength for pH < 7 and pH > 7 for Ir1 and Ir3. The emission sensing of biogenic amines with pka values ranging from 5.80 – 9.74 is reported along with cellular imaging. The complex Ir1 specifically localizes within lysosome (pH = 4.5 – 5) and thus image this organelle with great precision. The detail electronic spectra and electrochemical behaviour were reported here along with TDDFT results.
环甲基铱(III)与取代的苯并咪唑配合物:溶酶体内 pH 值定向的细胞器特异性定位
我们报告了四种发射性铱(III)配合物(Ir1 - Ir4)的合成和与 pH 值相关的发射光谱行为,这四种配合物具有两对异构的双三氟甲基附加苯并咪唑配体。两个配体中的咪唑氢(N-H)被苯基(N-Ph)取代,以了解氢键对配合物光物理性质的影响。在其中两种配合物中观察到了与 pH 值相关的电子光谱变化。Ir1 和 Ir3 在 pH < 7 和 pH > 7 的不同波长下,发射强度都有所增强。报告还介绍了对 pka 值在 5.80 - 9.74 之间的生物胺的发射传感以及细胞成像。复合物 Ir1 在溶酶体(pH = 4.5 - 5)内特异性定位,因此可以非常精确地对这一细胞器进行成像。本文报告了详细的电子光谱和电化学行为以及 TDDFT 结果。
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
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
×
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