Journal
JOURNAL OF COMPUTATIONAL CHEMISTRY
Volume 28, Issue 1, Pages 455-466Publisher
WILEY
DOI: 10.1002/jcc.20523
Keywords
resonance-assisted binding; resonance-assisted hydrogen binding; electrostatic interaction; block-localized wave function
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Block-localized wave function (BLW) method, which is a variant of the ab initio valence bond (VB) theory, was employed to explore the nature of resonance-assisted hydrogen bonds (RAHBs) and to investigate the mechanism of synergistic interplay between pi delocalization and hydrogen-bonding interactions. We examined the dimers of formic acid, formamide, 4-pyrimidinone, 2-pyridinone, 2-hydroxpyridine, and 2-hydroxycyclopenta-2,4dien-1-one. In addition, we studied the interactions in beta-diketone enols with a simplified model, namely the hydrogen bonds of 3-hydroxypropenal with both ethenol and formaldehyde. The intermolecular interaction energies, either with or without the involvement of pi resonance, were decomposed into the Hitler-London energy (Delta E-HL), polarization energy (Delta E-pol), charge transfer energy (Delta E-CT), and electron correlation energy (Delta E-cor) terms. This allows for the examination of the character of hydrogen bonds and the impact of pi conjugation on hydrogen bonding interactions. Although it has been proposed that resonance-assisted hydrogen bonds are accompanied with an increasing of covalency character, our analyses showed that the enhanced interactions mostly originate from the classical dipole-dipole (i.e., electrostatic) attraction, as resonance redistributes the electron density and increases the dipole moments in monomers. The covalency of hydrogen bonds, however, changes very little. This disputes the belief that RAHB is primarily covalent in nature. Accordingly, we recommend the term resonance-assisted binding (RAB) instead of resonance-assisted hydrogen bonding (RHAB) to highlight the electrostatic, which is a long-range effect, rather than the electron transfer nature of the enhanced stabilization in RAHBs. (C) 2006 Wiley Periodicals, Inc.
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