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Journal ArticleDOI

The hydrogen bond in the solid state.

Thomas Steiner
- 04 Jan 2002 - 
- Vol. 41, Iss: 1, pp 48-76
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TLDR
The hydrogen bond is the most important of all directional intermolecular interactions, operative in determining molecular conformation, molecular aggregation, and the function of a vast number of chemical systems ranging from inorganic to biological.
Abstract
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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Citations
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Measurement of two solvation regimes in water-ethanol mixtures using x-ray compton scattering.

TL;DR: The synchrotron x-ray Compton scattering technique is utilized to elucidate the structure of aqueous ethanol from a new experimental perspective and brings new light to evaluating the hypothesis of formation of clathratelike structures at the dilute concentrations.
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Syntheses and crystal structures of two novel zinc(II) coordination polymers

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Nature of the attractive interaction between proton acceptors and organic ring systems.

TL;DR: It is demonstrated that a major proportion of the interaction energy gain is originating from the non-adjacent moieties, that are not in close contact with the proton acceptor group.
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A comprehensive classification and nomenclature of carboxyl- carboxyl(ate) supramolecular motifs and related catemers: implications for biomolecular systems

TL;DR: The vast diversity of carboxyl–carboxyl(ate) arrangements is reduced to 17 supramolecular motifs and eight catemers, extracted from the CSD.
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Half-sandwich η6-benzene Ru(II) complexes of pyridylpyrazole and pyridylimidazole ligands : Synthesis, spectra, and structure

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References
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Journal ArticleDOI

van der Waals Volumes and Radii

Journal ArticleDOI

Patterns in Hydrogen Bonding: Functionality and Graph Set Analysis in Crystals

TL;DR: In this article, a review of the most promising systematic approaches to resolving this enigma was initially developed by the late M. C. Etter, who applied graph theory to recognize, and then utilize, patterns of hydrogen bonding for the understanding and design of molecular crystals.
Book

An Introduction to Hydrogen Bonding

TL;DR: In this paper, the authors discuss the properties of strong and moderate hydrogen bonds in biological molecules and include inclusion of inclusion compounds in the graph set theory of graph set theories, which is used in this paper.
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