Suppr超能文献

2-甲氧基苯酚在多壁碳纳米管上简便电化学脱甲基生成表面受限儿茶酚及其高效电催化肼氧化和传感应用

Facile Electrochemical Demethylation of 2-Methoxyphenol to Surface-Confined Catechol on the MWCNT and Its Efficient Electrocatalytic Hydrazine Oxidation and Sensing Applications.

作者信息

Gandhi Mansi, Rajagopal Desikan, Senthil Kumar Annamalai

机构信息

Nano and Bioelectrochemistry Research Laboratory, Department of Chemistry, School of Advanced Sciences, Vellore Institute of Technology University, Vellore 632014, India.

Department of Chemistry, School of Advanced Sciences, Vellore Institute of Technology University, Vellore 632014, India.

出版信息

ACS Omega. 2020 Jun 22;5(26):16208-16219. doi: 10.1021/acsomega.0c01846. eCollection 2020 Jul 7.

Abstract

Owing to its biological significance, preparation of stable surface-confined catechol (CA) is a long-standing interest in electrochemistry and surface chemistry. In this connection, various chemical approaches such as covalent immobilization (using amine- and carboxylate-functionalized CA, diazotization-based coupling, and Michael addition reaction), self-assembled monolayer on gold (thiol-functionalized CA is assembled on the gold surface), CA adsorption on the ad-layer of a defect-free single-crystal Pt surface, π-π bonding, CA pendant metal complexes, and CA-functionalized polymer-modified electrodes have been reported in the literature. In general, these conventional methods are involved with a series of time-consuming synthetic procedures. Indeed, the preparation of a surface-fouling-free surface-confined system is a challenging task. Herein, we introduce a new and facile approach based on electrochemical demethylation of 2-methoxyphenol as a precursor on the graphitic surface (MWCNT) at a bias potential, 0.5 V vs Ag/AgCl in neutral pH solution. Such an electrochemical performance resulted in the development of a stable and well-defined redox peak at ' = 0.15 (A2/C2) V vs Ag/AgCl within 10 min of preparation time in pH 7 phosphate buffer solution. Calculated surface excess (16.65 × 10 mol cm) is about 10-1000 times higher than the values reported with other preparation methods. The product (catechol) formed on the modified electrode was confirmed by collective electrochemical and physicochemical characterizations such as potential segment analysis, TEM, Raman, IR, UV-vis, GC-MS, and NMR spectroscopic techniques, and thin-layer chromatographic studies. The electrocatalytic efficiency of the surface-confined CA system was demonstrated by studying hydrazine oxidation and sensing reactions in a neutral pH solution. This new system is found to be tolerant to various interfering biochemicals such as uric acid, xanthine, hypoxanthine, glucose, nitrate, hydrogen peroxide, ascorbic acid, Cu, and Fe. Since the approach is simple, rapid, and reproducible, a variety of surface-confined CA systems can be prepared.

摘要

由于其生物学意义,制备稳定的表面受限儿茶酚(CA)一直是电化学和表面化学领域长期关注的问题。在这方面,文献中报道了各种化学方法,如共价固定(使用胺基和羧基功能化的CA、基于重氮化的偶联和迈克尔加成反应)、金表面的自组装单层(硫醇功能化的CA组装在金表面)、CA在无缺陷单晶Pt表面的吸附层上的吸附、π-π键合、CA悬垂金属配合物以及CA功能化聚合物修饰电极。一般来说,这些传统方法涉及一系列耗时的合成步骤。实际上,制备无表面污染的表面受限体系是一项具有挑战性的任务。在此,我们介绍一种基于在中性pH溶液中,以0.5 V对Ag/AgCl的偏压电位,在石墨表面(MWCNT)上对作为前体的2-甲氧基苯酚进行电化学脱甲基的新的简便方法。这种电化学性能导致在pH 7磷酸盐缓冲溶液中,在制备时间10分钟内,在' = 0.15(A2/C2)V对Ag/AgCl处出现稳定且明确的氧化还原峰。计算得到的表面过量(16.65×10 mol cm)比其他制备方法报道的值高约10 - 1000倍。通过电位分段分析、TEM、拉曼、红外、紫外可见、气相色谱 - 质谱和核磁共振光谱技术以及薄层色谱研究等综合电化学和物理化学表征,证实了修饰电极上形成的产物(儿茶酚)。通过研究中性pH溶液中的肼氧化和传感反应,证明了表面受限CA体系的电催化效率。发现这种新体系对各种干扰生化物质如尿酸、黄嘌呤、次黄嘌呤、葡萄糖、硝酸盐、过氧化氢、抗坏血酸、铜和铁具有耐受性。由于该方法简单、快速且可重复,因此可以制备各种表面受限的CA体系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d96a/7346242/cddb3def0ebb/ao0c01846_0001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验