Non-enzymatic glucose oxidation to gluconic acid with N, N′-bis(2-hydroxybenzylidineamino) benzene gold (III) complex

IF 1.7 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY
Sontara Konwar Boruah, Hirendra Das, Prabin Kumar Boruah
{"title":"Non-enzymatic glucose oxidation to gluconic acid with N, N′-bis(2-hydroxybenzylidineamino) benzene gold (III) complex","authors":"Sontara Konwar Boruah,&nbsp;Hirendra Das,&nbsp;Prabin Kumar Boruah","doi":"10.1007/s12039-023-02198-7","DOIUrl":null,"url":null,"abstract":"<div><p>In this paper we report non-enzymatic glucose oxidation with N, N′-Bis(2-hydroxybenzylidineamino) benzene gold (III) complex on reduced graphene oxide-gold (rGO-Au) nanoparticle coated modified copper (Cu) electrode. Potassium ferricyanide in 50 mM phosphate buffer solution (pH 7.0) was used as a mediator. The [(Salophen)Au]<sup>+</sup> on rGO shows good catalytic property for the oxidation of glucose to gluconic acid (GA). The maximum current response produced by Au<sup>3+</sup>/Au<sup>+</sup> redox potential was monitored by the linear sweep voltammetric method (LSV). As glucose concentration increases the current response at Au<sup>+3</sup>/Au<sup>+</sup> redox potential decreases simultaneously. On catalytic oxidation of glucose to GA by the complex [(Salophen)Au]<sup><b>+</b></sup>, the solution pH reduces to 2.75, which results the decrease of current responses at the Au<sup>3+</sup>/Au<sup>+</sup> working potential.</p><h3>Graphical abstract</h3><p>Direct oxidation of glucose to gluconic acid is achieved adopting non­enzytnatic technique by rGO based heterogeneous catalyst is reported in the present study. N,N'-Bis (2-hydroxy benzylidineatnino) benzene gold (III) complex on rGO-Au nanoparticles is used to fabricate the tnodified electrode. The oxidation mechanism is demonstrated. This work showed the potential of using [(Salophen)Au]<sup>+</sup> Schiff base complex as a non­enzymatic substitute for glucose oxidize enzyme.\n</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":616,"journal":{"name":"Journal of Chemical Sciences","volume":null,"pages":null},"PeriodicalIF":1.7000,"publicationDate":"2023-07-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Sciences","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s12039-023-02198-7","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

In this paper we report non-enzymatic glucose oxidation with N, N′-Bis(2-hydroxybenzylidineamino) benzene gold (III) complex on reduced graphene oxide-gold (rGO-Au) nanoparticle coated modified copper (Cu) electrode. Potassium ferricyanide in 50 mM phosphate buffer solution (pH 7.0) was used as a mediator. The [(Salophen)Au]+ on rGO shows good catalytic property for the oxidation of glucose to gluconic acid (GA). The maximum current response produced by Au3+/Au+ redox potential was monitored by the linear sweep voltammetric method (LSV). As glucose concentration increases the current response at Au+3/Au+ redox potential decreases simultaneously. On catalytic oxidation of glucose to GA by the complex [(Salophen)Au]+, the solution pH reduces to 2.75, which results the decrease of current responses at the Au3+/Au+ working potential.

Graphical abstract

Direct oxidation of glucose to gluconic acid is achieved adopting non­enzytnatic technique by rGO based heterogeneous catalyst is reported in the present study. N,N'-Bis (2-hydroxy benzylidineatnino) benzene gold (III) complex on rGO-Au nanoparticles is used to fabricate the tnodified electrode. The oxidation mechanism is demonstrated. This work showed the potential of using [(Salophen)Au]+ Schiff base complex as a non­enzymatic substitute for glucose oxidize enzyme.

Abstract Image

用N, N ' -双(2-羟基苄基氨基)苯金(III)配合物非酶促葡萄糖氧化制葡萄糖酸
在本文中,我们报道了N, N ' -双(2-羟基苄基氨基)苯金(III)配合物在还原氧化石墨烯-金(rGO-Au)纳米颗粒包覆的修饰铜(Cu)电极上非酶氧化葡萄糖。采用50 mM磷酸盐缓冲液(pH 7.0)中的铁氰化钾作为介质。还原氧化石墨烯上的[(Salophen)Au]+对葡萄糖氧化制葡萄糖酸(GA)具有良好的催化性能。采用线性扫描伏安法(LSV)监测了Au3+/Au+氧化还原电位产生的最大电流响应。随着葡萄糖浓度的增加,Au+3/Au+氧化还原电位的电流响应同时降低。配合物[(Salophen)Au]+催化葡萄糖氧化制GA时,溶液pH降至2.75,导致在Au3+/Au+工作电位处电流响应降低。摘要本文报道了采用非酶催化技术,以氧化石墨烯为基础的多相催化剂,实现了葡萄糖直接氧化制葡萄糖酸。采用N,N'-双(2-羟基苄基苯基尼诺)苯金(III)配合物在氧化石墨烯-金纳米颗粒上制备二甲基化电极。证明了氧化机理。本研究显示了[(Salophen)Au]+希夫碱配合物作为葡萄糖氧化酶的非酶替代品的潜力。
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
Journal of Chemical Sciences
Journal of Chemical Sciences CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
3.10
自引率
5.90%
发文量
107
审稿时长
1 months
期刊介绍: Journal of Chemical Sciences is a monthly journal published by the Indian Academy of Sciences. It formed part of the original Proceedings of the Indian Academy of Sciences – Part A, started by the Nobel Laureate Prof C V Raman in 1934, that was split in 1978 into three separate journals. It was renamed as Journal of Chemical Sciences in 2004. The journal publishes original research articles and rapid communications, covering all areas of chemical sciences. A significant feature of the journal is its special issues, brought out from time to time, devoted to conference symposia/proceedings in frontier areas of the subject, held not only in India but also in other countries.
×
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