Stimuli-responsive Zn(ii) complexes showing the structural conversion and on/off switching of catalytic properties†

IF 3.9 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
RSC Advances Pub Date : 2024-10-16 DOI:10.1039/D4RA06058J
So Hyeon Kwon, Sunwoo Lee, Jacopo Tessarolo and Haeri Lee
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引用次数: 0

Abstract

In this work, we report a series of dinuclear Zn(II) complexes and their corresponding catalytic properties for a transesterification reaction. We show that the structures and catalytic activity of the complexes are strongly dependent on their molecular structures surrounding the metal centres. The use of halides yields a series of [Zn2X4L] (X = Cl, Br, and I) complexes with low catalytic activity because of the fully saturated coordination environment, whereas Zn(ClO4)2 results in two isomeric [ZnL]n 1D coordination polymers with efficient catalytic properties, despite being susceptible to structural rearrangement and consequent changes in catalytic activity over time. The response to chemical stimuli to trigger anion exchange allows for switching on/off the systems' catalytic activity, simultaneously recovering the catalytic effect upon degradation and thus reconstructing the coordination environment of the 1D polymer.

显示催化特性结构转换和开关切换的刺激响应型 Zn(ii) 复合物†。
在这项研究中,我们报告了一系列双核锌(II)配合物及其在酯交换反应中的相应催化特性。我们发现,配合物的结构和催化活性在很大程度上取决于围绕金属中心的分子结构。使用卤化物会产生一系列[Zn2X4L](X = Cl、Br 和 I)配合物,由于完全饱和的配位环境,这些配合物的催化活性较低;而 Zn(ClO4)2 则会产生两种同分异构的[ZnL]n 一维配位聚合物,它们具有高效的催化特性,尽管随着时间的推移容易发生结构重排并导致催化活性发生变化。通过对化学刺激的响应来触发阴离子交换,可以开启/关闭系统的催化活性,同时在降解时恢复催化效果,从而重建一维聚合物的配位环境。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
RSC Advances
RSC Advances chemical sciences-
CiteScore
7.50
自引率
2.60%
发文量
3116
审稿时长
1.6 months
期刊介绍: An international, peer-reviewed journal covering all of the chemical sciences, including multidisciplinary and emerging areas. RSC Advances is a gold open access journal allowing researchers free access to research articles, and offering an affordable open access publishing option for authors around the world.
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