用于荧光识别硫酸氢的芘-钙[4]三唑鎓共轭物

IF 4.6 1区 化学 Q1 CHEMISTRY, ORGANIC Organic Chemistry Frontiers Pub Date : 2024-06-13 DOI:10.1039/d4qo00704b
Jihee Cho, Rakesh Parida, Changhyun Lim, Jin Yong Lee, Jong Seung Kim, Sanghee Kim
{"title":"用于荧光识别硫酸氢的芘-钙[4]三唑鎓共轭物","authors":"Jihee Cho, Rakesh Parida, Changhyun Lim, Jin Yong Lee, Jong Seung Kim, Sanghee Kim","doi":"10.1039/d4qo00704b","DOIUrl":null,"url":null,"abstract":"A new fluorescent sensor was developed, in which pyrene is conjugated to calix[4]triazolium via an ester linker, and its ability to bind anions was investigated. Interestingly, addition of HSO4- to Py-CT4 resulted in increased fluorescence, but other anions had little effect. This phenomenon is attributed to the formation of a 1:1 stoichiometric Py-CT4-HSO4- complex that interferes with the photoinduced electron transfer (PET) process. The selectivity of Py-CT4 for HSO4− is the result of appropriate spatial complementarity to, and hydrogen bond interaction with, HSO4−. The binding mode and fluorescence changes caused by the PET process can be explained well by density functional theory (DFT) calculations.","PeriodicalId":97,"journal":{"name":"Organic Chemistry Frontiers","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-06-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A Pyrene-Calix[4]triazolium Conjugate for Fluorescence Recognition of Hydrogen Sulfate\",\"authors\":\"Jihee Cho, Rakesh Parida, Changhyun Lim, Jin Yong Lee, Jong Seung Kim, Sanghee Kim\",\"doi\":\"10.1039/d4qo00704b\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A new fluorescent sensor was developed, in which pyrene is conjugated to calix[4]triazolium via an ester linker, and its ability to bind anions was investigated. Interestingly, addition of HSO4- to Py-CT4 resulted in increased fluorescence, but other anions had little effect. This phenomenon is attributed to the formation of a 1:1 stoichiometric Py-CT4-HSO4- complex that interferes with the photoinduced electron transfer (PET) process. The selectivity of Py-CT4 for HSO4− is the result of appropriate spatial complementarity to, and hydrogen bond interaction with, HSO4−. The binding mode and fluorescence changes caused by the PET process can be explained well by density functional theory (DFT) calculations.\",\"PeriodicalId\":97,\"journal\":{\"name\":\"Organic Chemistry Frontiers\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2024-06-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic Chemistry Frontiers\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1039/d4qo00704b\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic Chemistry Frontiers","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d4qo00704b","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0

摘要

我们开发了一种新型荧光传感器,其中芘通过酯连接体与钙[4]三唑鎓共轭,并研究了其与阴离子结合的能力。有趣的是,在 Py-CT4 中加入 HSO4- 会导致荧光增加,而其他阴离子则影响不大。这一现象归因于形成了 1:1 的 Py-CT4-HSO4- 配位复合物,干扰了光诱导电子转移(PET)过程。Py-CT4 对 HSO4- 的选择性是与 HSO4- 适当的空间互补性和氢键相互作用的结果。密度泛函理论(DFT)计算可以很好地解释 PET 过程引起的结合模式和荧光变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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
A Pyrene-Calix[4]triazolium Conjugate for Fluorescence Recognition of Hydrogen Sulfate
A new fluorescent sensor was developed, in which pyrene is conjugated to calix[4]triazolium via an ester linker, and its ability to bind anions was investigated. Interestingly, addition of HSO4- to Py-CT4 resulted in increased fluorescence, but other anions had little effect. This phenomenon is attributed to the formation of a 1:1 stoichiometric Py-CT4-HSO4- complex that interferes with the photoinduced electron transfer (PET) process. The selectivity of Py-CT4 for HSO4− is the result of appropriate spatial complementarity to, and hydrogen bond interaction with, HSO4−. The binding mode and fluorescence changes caused by the PET process can be explained well by density functional theory (DFT) calculations.
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
Organic Chemistry Frontiers
Organic Chemistry Frontiers CHEMISTRY, ORGANIC-
CiteScore
7.90
自引率
11.10%
发文量
686
审稿时长
1 months
期刊介绍: Organic Chemistry Frontiers is an esteemed journal that publishes high-quality research across the field of organic chemistry. It places a significant emphasis on studies that contribute substantially to the field by introducing new or significantly improved protocols and methodologies. The journal covers a wide array of topics which include, but are not limited to, organic synthesis, the development of synthetic methodologies, catalysis, natural products, functional organic materials, supramolecular and macromolecular chemistry, as well as physical and computational organic chemistry.
期刊最新文献
A Ligand-assisted Manganese-enabled Direct C-H Difluoromethylation of Arenes Photoredox-Enabled Ring-Opening of Cyclobutanes via the Formation of a Carbon Radical Asymmetric Synthesis of 1H-pyrazolo[3,4-b]pyridine Analogues Catalyzed by Chiral-at-Metal Rh(III) Complexes Total Synthesis of (‒)-Deglycocadambine Copper-Catalyzed Allenynylative C–P Couplings of Diynylic Acetates with Hydrophosphoryl Compounds Leading to Phosphorylated Allenynes
×
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
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:481959085
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