Fang Yu, Powell Joshua A, Li Errui, Wang Qi, Perry Zachary, Kirchon Angelo, Yang Xinyu, Xiao Zhifeng, Zhu Chengfeng, Zhang Liangliang, Huang Feihe, Zhou Hong-Cai
Department of Chemistry, Texas A&M University, College Station, Texas 77842-3012, USA.
Chem Soc Rev. 2019 Aug 27;48(17):4707-4730. doi: 10.1039/c9cs00091g.
Natural enzymes catalyze reactions in their substrate-binding cavities, exhibiting high specificity and efficiency. In an effort to mimic the structure and functionality of enzymes, discrete coordination cages were designed and synthesized. These self-assembled systems have a variety of confined cavities, which have been applied to accelerate conventional reactions, perform substrate-specific reactions, and manipulate regio- and enantio-selectivity. Many coordination cages or cage-catalyst composites have achieved unprecedented results, outperforming their counterparts in different catalytic reactions. This tutorial review summarizes recent developments of coordination cages across three key approaches to coordination cage catalysis: (1) cavity promoted reactions, (2) embedding of active sites in the structure of the cage, and (3) encapsulation of catalysts within the cage. Special emphasis of the review involves (1) introduction of the structure and property of the coordination cage, (2) discussion of the catalytic pathway mediated by the cage, (3) elucidation of the structure-property relationship between the cage and the designated reaction. This work will summarize the recent progress in supramolecular catalysis and attract more researchers to pursue cavity-promoted reactions using discrete coordination cages.
天然酶在其底物结合腔内催化反应,具有高度的特异性和效率。为了模拟酶的结构和功能,人们设计并合成了离散的配位笼。这些自组装体系具有多种受限腔,已被用于加速传统反应、进行底物特异性反应以及控制区域和对映选择性。许多配位笼或笼-催化剂复合材料都取得了前所未有的成果,在不同的催化反应中表现优于同类材料。本教程综述总结了配位笼在配位笼催化的三种关键方法中的最新进展:(1)腔促进反应,(2)在笼结构中嵌入活性位点,(3)将催化剂封装在笼内。该综述特别强调:(1)介绍配位笼的结构和性质,(2)讨论由笼介导的催化途径,(3)阐明笼与指定反应之间的结构-性质关系。这项工作将总结超分子催化的最新进展,并吸引更多研究人员利用离散配位笼进行腔促进反应。