Fluorescent Calix[4]arene-Oxacyclophane Sensor for Transition Metal Cations

Alexandra I. Costa, Patrícia D. Barata, J. V. Prata
{"title":"Fluorescent Calix[4]arene-Oxacyclophane Sensor for Transition Metal Cations","authors":"Alexandra I. Costa, Patrícia D. Barata, J. V. Prata","doi":"10.3390/ECSOC-24-08453","DOIUrl":null,"url":null,"abstract":"The sensing behavior of a calix[4]arene-oxacyclophane-carbazole conjugate (1) towards Cu(I) ions was investigated. Contrary to the noteworthy sensitivity and selectivity previously found for Cu(II), the affinity of 1 for Cu(I) cations is much lower. Through fluorescence titration assays, the apparent binding constants (Ka) for the two ions were determined, showing that an affinity of over thirteen fold was displayed for Cu(II). Two Cu(I) counter-ions were used to determine possible effects on the binding event. It was found that acetate and iodide ions behave similarly, yielding Ka of the same magnitude. Formation of a ground-state supramolecular complex between 1 and Cu(I) ions was not observed on UV-Vis titrations, in contrast to what was previously reported for Cu(II) using the same host. The affinity of 1 for Fe(III), a major biological competitor, was also assessed. The fluorescence of host 1 is quenched by Fe(III) ions although to a lesser extent (32% less efficient than Cu(II)). The study demonstrates that calixarene 1 is able to differentiate copper ions in two common oxidation states using fluorescence techniques, thereby suggesting its application for redox-active centers in biomimetic chemistry.","PeriodicalId":9815,"journal":{"name":"Chemistry Proceedings","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2020-11-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemistry Proceedings","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/ECSOC-24-08453","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The sensing behavior of a calix[4]arene-oxacyclophane-carbazole conjugate (1) towards Cu(I) ions was investigated. Contrary to the noteworthy sensitivity and selectivity previously found for Cu(II), the affinity of 1 for Cu(I) cations is much lower. Through fluorescence titration assays, the apparent binding constants (Ka) for the two ions were determined, showing that an affinity of over thirteen fold was displayed for Cu(II). Two Cu(I) counter-ions were used to determine possible effects on the binding event. It was found that acetate and iodide ions behave similarly, yielding Ka of the same magnitude. Formation of a ground-state supramolecular complex between 1 and Cu(I) ions was not observed on UV-Vis titrations, in contrast to what was previously reported for Cu(II) using the same host. The affinity of 1 for Fe(III), a major biological competitor, was also assessed. The fluorescence of host 1 is quenched by Fe(III) ions although to a lesser extent (32% less efficient than Cu(II)). The study demonstrates that calixarene 1 is able to differentiate copper ions in two common oxidation states using fluorescence techniques, thereby suggesting its application for redox-active centers in biomimetic chemistry.
过渡金属阳离子荧光杯[4]芳烃-氧环烷传感器
研究了杯状[4]芳烃-氧环番-咔唑缀合物(1)对Cu(I)离子的传感行为。与之前发现的对Cu(II)的敏感性和选择性相反,1对Cu(I)阳离子的亲和力要低得多。通过荧光滴定法测定了两种离子的表观结合常数(Ka),表明对Cu(II)的亲和力超过13倍。使用两个Cu(I)反离子来确定可能对结合事件的影响。发现醋酸离子和碘离子的行为相似,产生相同大小的Ka。在UV-Vis滴定中没有观察到1和Cu(I)离子之间形成基态超分子络合物,这与之前报道的使用相同宿主的Cu(II)形成了对比。还评估了1对主要生物竞争对手铁(III)的亲和力。宿主1的荧光被Fe(III)离子猝灭,尽管程度较低(比Cu(II)低32%)。该研究表明,杯芳烃1能够利用荧光技术区分铜离子在两种常见的氧化态,从而提示其在仿生化学中的氧化活性中心的应用。
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
自引率
0.00%
发文量
0
×
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