The Hydrogen Bond in the Solid State

氢键 范德瓦尔斯力 共价键 化学 分子间力 化学物理 六重键 离子键合 离解(化学) 化学键 低势垒氢键 非共价相互作用 合并(版本控制) 伦敦分散部队 计算化学 债券定单 分子 粘结长度 物理化学 有机化学 离子 计算机科学 情报检索
作者
Thomas Steiner
出处
期刊:Angewandte Chemie [Wiley]
卷期号:41 (1): 48-76 被引量:6092
标识
DOI:10.1002/1521-3773(20020104)41:1<48::aid-anie48>3.0.co;2-u
摘要

The hydrogen bond is the most important of all directional intermolecular interactions. It is operative in determining molecular conformation, molecular aggregation, and the function of a vast number of chemical systems ranging from inorganic to biological. Research into hydrogen bonds experienced a stagnant period in the 1980s, but re-opened around 1990, and has been in rapid development since then. In terms of modern concepts, the hydrogen bond is understood as a very broad phenomenon, and it is accepted that there are open borders to other effects. There are dozens of different types of X-H.A hydrogen bonds that occur commonly in the condensed phases, and in addition there are innumerable less common ones. Dissociation energies span more than two orders of magnitude (about 0.2-40 kcal mol(-1)). Within this range, the nature of the interaction is not constant, but its electrostatic, covalent, and dispersion contributions vary in their relative weights. The hydrogen bond has broad transition regions that merge continuously with the covalent bond, the van der Waals interaction, the ionic interaction, and also the cation-pi interaction. All hydrogen bonds can be considered as incipient proton transfer reactions, and for strong hydrogen bonds, this reaction can be in a very advanced state. In this review, a coherent survey is given on all these matters.
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