Issue 64, 2004

The strength–length relationship at the light of ab initio computations: does it really hold?

Abstract

The validity of the so-called strength–length correlation (“the shorter the contact, the stronger it is”) has been evaluated for short O–H⋯O contacts by correlating the MP2 interaction energy with the O–H⋯O distance. This correlation has been carried out for all the dimolecular systems that present short O–H⋯O contacts with the metric expected for hydrogen bonds, within the set of neutron diffraction crystals deposited in the Cambridge Crystallographic Database (CSD). Using the crystal geometry of these dimolecular systems and the 6-31+G(d) basis set, we calculated their MP2 interaction energy (corrected by the BSSE error). We also computed the components of that interaction energy using the IMPT method of Stone. No correlation is found between the MP2 interaction energy and the H⋯O distance when all dimolecular systems are analysed together. The IMPT analysis shows that this is due to the different nature of the interaction energy for charged fragments compared to that for neutral fragments. When the charge⋯charge dimolecular systems are discarded, the interaction energy of the remaining systems is found to follow a trend that roughly resembles the shape of the 1/rO⋯H2 or 1/rO⋯H4 curves (rO⋯H = H⋯O distance), although with very wide deviations. Consequently, one should only use strength–length correlations when the correlated dimolecular systems present a similar behaviour of their interaction energies with the distance.

Graphical abstract: The strength–length relationship at the light of ab initio computations: does it really hold?

Article information

Article type
Paper
Submitted
04 may. 2004
Accepted
13 jul. 2004
First published
17 sep. 2004

CrystEngComm, 2004,6, 368-376

The strength–length relationship at the light of ab initio computations: does it really hold?

E. D'Oria and J. J. Novoa, CrystEngComm, 2004, 6, 368 DOI: 10.1039/B406743F

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