Journal of Chemical Physics 111 , 7727-7735 (1999)

Anne Milet^b, Tatiana Korona^a, Robert Moszynski^a,b, and Elise Kochanski^a,b

^a Department of Chemistry, University of Warsaw, Pasteura 1, 02-093 Warsaw, Poland
^b Laboratoire de Chimie Théorique, Université Louis Pasteur, 4, rue Blaise Pascal, 67070 Strasbourg, France

Anisotropic intermolecular interactions in van der Waals and hydrogen-bonded complexes: what can we get from density functional calculations?

Abstract

The applicability of various density functional theories (DFT) to describe the anisotropy of the intermolecular potential energy surfaces of hydrogen-bonded [OH^--H₂O, (H₂O)₂] and van der Waals [CO-H₂O, He-CO₂] complexes has been tested by comparison with supermolecule CCSD(T) (coupled-cluster method restricted to single, double, and noniterative triple excitations) and perturbational SAPT (symmetry-adapted perturtabional theory) results computed for the same geometries and with the same basis sets. It is shown that for strongly bound ionic hydrogen-bonded complexes, like OH^--H₂O, hybrid approaches provide accurate results. For other systems, including the water dimer, the DFT calculations fail to reproduce the correct angular dependence of the potential surfaces. It is also shown that a hybrid functional adjusted to reproduce the CCSD(T) value of the binding energy for the water dimer produces results worse than the standard hybrid functionals for OH^--H₂O, and fails to describe the correct anisotropy of the CO-H₂O interaction.

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