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金属配位导向大环配合物的合成方法。

Synthetic approaches to metal-coordination-directed macrocyclic complexes.

作者信息

Fang Qingqing, Xu Yan, Yan Xiaosheng, Jiang Tao, Jiang Yunbao

机构信息

Department of Chemistry, College of Chemistry and Chemical Engineering, The MOE Key Laboratory of Spectrochemical Analysis and Instrumentation, and iChEM, Xiamen University, Xiamen, China.

Songshan Academy, Zhengzhou University of Aeronautics, Zhengzhou, China.

出版信息

Front Chem. 2022 Nov 24;10:1078432. doi: 10.3389/fchem.2022.1078432. eCollection 2022.

Abstract

Metal-coordination-directed macrocyclic complexes, in which macrocyclic architectures are formed by metal-ligand coordination interactions, have emerged as attractive supramolecular scaffolds for the creation of materials for applications in biosensing and therapeutics. Despite recent progress, uncontrolled multicyclic cages and linear oligomers/polymers is the most likely outcome from metal-ligands assembly, representing a challenge to current synthetic methods. Herein we outlined the state-of-art synthetic approaches to the metal-coordination-directed macrocyclic complexes by using foldable ligands or through assembly of amphiphilic ligands. This mini-review offers a guideline for the efficient preparation of metal-coordination-directed macrocyclic complexes with predictable and controllable structures, which may find applications in many biology-related areas.

摘要

金属配位导向的大环配合物,其中大环结构是通过金属-配体配位相互作用形成的,已成为用于创建生物传感和治疗应用材料的有吸引力的超分子支架。尽管最近取得了进展,但金属-配体组装最可能产生不受控制的多环笼和线性低聚物/聚合物,这对当前的合成方法构成了挑战。在此,我们概述了通过使用可折叠配体或通过两亲性配体组装来合成金属配位导向大环配合物的最新方法。这篇综述为高效制备具有可预测和可控结构的金属配位导向大环配合物提供了指导,这些配合物可能在许多生物学相关领域找到应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95ed/9731519/f8e6ec894e7a/fchem-10-1078432-g001.jpg

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