阳离子聚合
电负性
催化作用
星团(航天器)
离子半径
离子键合
金属
无机化学
齿合度
氢键
结晶学
离子
高分子化学
化学
分子
计算机科学
有机化学
程序设计语言
作者
Naoki Ogiwara,Sayaka Uchida
出处
期刊:Chem catalysis
[Elsevier]
日期:2023-04-21
卷期号:3 (7): 100607-100607
被引量:10
标识
DOI:10.1016/j.checat.2023.100607
摘要
This review discusses the catalysis of metal–oxo-cluster-based crystals. The catalytically active metal–oxo cluster anions (polyoxometalates [POMs]) can be solidified with inorganic cations, organic cations, cationic metal complexes, or cationic coordination polymers (CPs). The spatial periodicity of POMs, which is closely associated with their catalysis, can be engineered via electrostatic interaction, hydrogen bonds, or coordination bonds by appropriately choosing the cations above. We also refer to less common cationic metal–oxo clusters. The catalytic properties of metal–oxo clusters, such as acid/base and redox, can be controlled by the charge, electron configuration, ionic radius, or electronegativity of their constituent elements. Similarly, the properties of their counterparts (inorganic or organic ions, metal complexes, and CPs) can be designed by their nuclearity, denticity, or ligands. Therefore, the infinite combination of anions and cations would enable construction of a large variety of crystals, contributing to the development of catalytic science.
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