溶剂化
化学
二甲基甲酰胺
乙腈
协调数
水溶液中的金属离子
离子
金属
配位复合体
无机化学
氨
电子供体
溶剂
有机化学
催化作用
标识
DOI:10.1039/bk9781839169601-00120
摘要
This chapter summarizes the experimentally reported structures of hydrated and solvated metal ions in solution and the solid state. The oxygen donor solvents dimethylsulfoxide, N,N-dimethylformamide, and N,N′-dimethylpropyleneurea and the nitrogen donor solvents acetonitrile and liquid ammonia have been selected because a relatively large number of solvate structures, in both the solid state and solution, have been reported. Their bonding characteristics are fairly different and can therefore act as models for a wide range of solvents. N,N′-Dimethylpropyleneurea is selected as it is space-demanding upon coordination forcing many metal ions to adopt lower coordination numbers than for most oxygen donor solvents. The physico-chemical impact of a lower coordination number with low symmetry is discussed. Liquid ammonia is representative for solvents with a strong electron-pair donor ability, and the impact on the coordination chemistry is discussed.
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