Ab initio study of the intermolecular potential of Ar–H2O.

The combination of supermolecular Mo\ller–Plesset treatment with the perturbation theory of intermolecular forces is applied in the analysis of the potential-energy surface of Ar–H2O. The surface is very isotropic with the lowest barrier for rotation of ∼35 cm-1 above the absolute minimum. The lower bound for De is found to be 108 cm-1 and the complex reveals a very floppy structure, with Ar moving freely from the H-bridged structure to the coplanar and almost perpendicular arrangement of the C2 –water axis and the Ar–O axis, ‘‘T-shaped’’ structure. This motion is almost isoenergetic (energy change of less than 2 cm-1 ). The H-bridged structure is favored by the attractive induction and dispersion anisotropies; the T-shaped structure is favored by repulsive exchange anisotropy. The nonadditive effect in the Ar2–H2O cluster was also calculated. Implications of our results on the present models of hydrophobic interactions are also discussed. [ABSTRACT FROM AUTHOR]