使用基于二茂铁的多位苯并咪唑受体对阴离子进行电化学和光学识别研究

IF 2.1 3区 化学 Q3 CHEMISTRY, INORGANIC & NUCLEAR Journal of Organometallic Chemistry Pub Date : 2024-09-06 DOI:10.1016/j.jorganchem.2024.123370
Ji-Bin Zhuo , Jian-Feng Yan , Yao-Feng Yuan
{"title":"使用基于二茂铁的多位苯并咪唑受体对阴离子进行电化学和光学识别研究","authors":"Ji-Bin Zhuo ,&nbsp;Jian-Feng Yan ,&nbsp;Yao-Feng Yuan","doi":"10.1016/j.jorganchem.2024.123370","DOIUrl":null,"url":null,"abstract":"<div><p>A novel multi-site receptor <strong>1</strong> bearing four ferrocenyl arms comprising benzimidazolium moieties was synthesized and structurally characterized by IR, NMR, elemental analysis, mass spectra. Moreover, the structure of receptor <strong>1</strong> was confirmed by X-ray crystallography, it was clear that the cationic heterocyclic was interacted with PF<sub>6</sub><sup>−</sup> through C–H···F hydrogen bonds. Its electrochemical properties of sensing the various anions were investigated by cyclic voltammograms (CV) and differential pulse voltammetry (DPV), the receptor <strong>1</strong> displayed a significant cathodic shift for <em>F</em><sup>−</sup>and OH<sup>−</sup>. The addition of <em>F</em><sup>−</sup> and OH<sup>−</sup>to the solution of receptor <strong>1</strong> resulted in obvious absorption changes in the UV–Vis spectrum, showing that receptor <strong>1</strong> was an excellent sensor for these analytes (<em>F</em><sup>−</sup>: LOD = 3.11 × 10<sup>−6</sup> M, LOQ = 1.03 × 10<sup>−5</sup> M, <em>K<sub>a</sub></em> = 5.83 × 10<sup>5</sup> <em>M</em><sup>−1</sup>; and OH<sup>–</sup>: LOD = 1.36 × 10<sup>−6</sup> M, LOQ = 4.11 × 10<sup>−5</sup> M, <em>K<sub>a</sub></em> = 9.03 × 10<sup>5</sup> <em>M</em><sup>−1</sup>). <sup>1</sup>H NMR titrations demonstrated that anion was recognized by receptor <strong>1</strong> through (C–H)<sup>+</sup>···<em>X</em><sup>−</sup> and C–H···X hydrogen bonds, the binding process involve initial formation of hydrogen bond and followed by deprotonation.</p></div>","PeriodicalId":374,"journal":{"name":"Journal of Organometallic Chemistry","volume":"1021 ","pages":"Article 123370"},"PeriodicalIF":2.1000,"publicationDate":"2024-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Electrochemical and optical recognition studies of anions using a multi-site ferrocene-based benzimidazolium receptor\",\"authors\":\"Ji-Bin Zhuo ,&nbsp;Jian-Feng Yan ,&nbsp;Yao-Feng Yuan\",\"doi\":\"10.1016/j.jorganchem.2024.123370\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>A novel multi-site receptor <strong>1</strong> bearing four ferrocenyl arms comprising benzimidazolium moieties was synthesized and structurally characterized by IR, NMR, elemental analysis, mass spectra. Moreover, the structure of receptor <strong>1</strong> was confirmed by X-ray crystallography, it was clear that the cationic heterocyclic was interacted with PF<sub>6</sub><sup>−</sup> through C–H···F hydrogen bonds. Its electrochemical properties of sensing the various anions were investigated by cyclic voltammograms (CV) and differential pulse voltammetry (DPV), the receptor <strong>1</strong> displayed a significant cathodic shift for <em>F</em><sup>−</sup>and OH<sup>−</sup>. The addition of <em>F</em><sup>−</sup> and OH<sup>−</sup>to the solution of receptor <strong>1</strong> resulted in obvious absorption changes in the UV–Vis spectrum, showing that receptor <strong>1</strong> was an excellent sensor for these analytes (<em>F</em><sup>−</sup>: LOD = 3.11 × 10<sup>−6</sup> M, LOQ = 1.03 × 10<sup>−5</sup> M, <em>K<sub>a</sub></em> = 5.83 × 10<sup>5</sup> <em>M</em><sup>−1</sup>; and OH<sup>–</sup>: LOD = 1.36 × 10<sup>−6</sup> M, LOQ = 4.11 × 10<sup>−5</sup> M, <em>K<sub>a</sub></em> = 9.03 × 10<sup>5</sup> <em>M</em><sup>−1</sup>). <sup>1</sup>H NMR titrations demonstrated that anion was recognized by receptor <strong>1</strong> through (C–H)<sup>+</sup>···<em>X</em><sup>−</sup> and C–H···X hydrogen bonds, the binding process involve initial formation of hydrogen bond and followed by deprotonation.</p></div>\",\"PeriodicalId\":374,\"journal\":{\"name\":\"Journal of Organometallic Chemistry\",\"volume\":\"1021 \",\"pages\":\"Article 123370\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2024-09-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Organometallic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0022328X24003656\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Organometallic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0022328X24003656","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0

摘要

通过红外光谱、核磁共振、元素分析和质谱分析,合成了一种新型多位点受体 1,该受体含有四个由苯并咪唑分子组成的二茂铁臂。此外,X 射线晶体学还证实了受体 1 的结构,阳离子杂环显然是通过 C-H-F 氢键与 PF6- 相互作用的。通过循环伏安图(CV)和微分脉冲伏安法(DPV)研究了受体1感知各种阴离子的电化学特性。在受体 1 的溶液中加入 F- 和 OH- 会导致紫外可见光谱中出现明显的吸收变化,这表明受体 1 对这些分析物具有极佳的传感器性能(F-:LOD = 3.11 × 10-6 M,LOQ = 1.03 × 10-5 M,Ka = 5.83 × 105 M-1;OH-:LOD = 1.36 × 10-6 M,LOQ = 1.03 × 10-5 M,Ka = 5.83 × 105 M-1):LOD = 1.36 × 10-6 M,LOQ = 4.11 × 10-5 M,Ka = 9.03 × 105 M-1)。1H NMR 滴定结果表明,阴离子是通过(C-H)+--X-和 C-H---X 氢键被受体 1 识别的,结合过程包括氢键的初始形成和随后的去质子化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

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
Electrochemical and optical recognition studies of anions using a multi-site ferrocene-based benzimidazolium receptor

A novel multi-site receptor 1 bearing four ferrocenyl arms comprising benzimidazolium moieties was synthesized and structurally characterized by IR, NMR, elemental analysis, mass spectra. Moreover, the structure of receptor 1 was confirmed by X-ray crystallography, it was clear that the cationic heterocyclic was interacted with PF6 through C–H···F hydrogen bonds. Its electrochemical properties of sensing the various anions were investigated by cyclic voltammograms (CV) and differential pulse voltammetry (DPV), the receptor 1 displayed a significant cathodic shift for Fand OH. The addition of F and OHto the solution of receptor 1 resulted in obvious absorption changes in the UV–Vis spectrum, showing that receptor 1 was an excellent sensor for these analytes (F: LOD = 3.11 × 10−6 M, LOQ = 1.03 × 10−5 M, Ka = 5.83 × 105 M−1; and OH: LOD = 1.36 × 10−6 M, LOQ = 4.11 × 10−5 M, Ka = 9.03 × 105 M−1). 1H NMR titrations demonstrated that anion was recognized by receptor 1 through (C–H)+···X and C–H···X hydrogen bonds, the binding process involve initial formation of hydrogen bond and followed by deprotonation.

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
Journal of Organometallic Chemistry
Journal of Organometallic Chemistry 化学-无机化学与核化学
CiteScore
4.40
自引率
8.70%
发文量
221
审稿时长
36 days
期刊介绍: The Journal of Organometallic Chemistry targets original papers dealing with theoretical aspects, structural chemistry, synthesis, physical and chemical properties (including reaction mechanisms), and practical applications of organometallic compounds. Organometallic compounds are defined as compounds that contain metal - carbon bonds. The term metal includes all alkali and alkaline earth metals, all transition metals and the lanthanides and actinides in the Periodic Table. Metalloids including the elements in Group 13 and the heavier members of the Groups 14 - 16 are also included. The term chemistry includes syntheses, characterizations and reaction chemistry of all such compounds. Research reports based on use of organometallic complexes in bioorganometallic chemistry, medicine, material sciences, homogeneous catalysis and energy conversion are also welcome. The scope of the journal has been enlarged to encompass important research on organometallic complexes in bioorganometallic chemistry and material sciences, and of heavier main group elements in organometallic chemistry. The journal also publishes review articles, short communications and notes.
期刊最新文献
Recent progress in synthesis, reactivity, and biological activities of selenopheno[2,3-c/3,2-c] pyrazole heterocycles DFT study on the mechanism and structural aspects of iron(II)-catalyzed condensation of epichlorohydrin and CO2 2,3-diferrocenyl-(1-triphenylphosphoranylidene)ketene: Synthesis and interactions with O, C, N, S, Se nucleophiles, characterization and X-ray diffraction Recyclable and reusable Pd(acac)2/BrettPhos/PEG-1000 system for the Suzuki-Miyaura coupling of nitroarenes Recent advances in homogeneous catalysts for the acceptorless dehydrogenation of alcohols to ketones and aldehydes
×
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: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