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Analysis of the potential energy surface of Ar–NH3
The Journal of Chemical Physics (1989)
  • G. Chalasinski
  • S. M. Cybulski
  • M. M. Szczesniak
  • Steve Scheiner, Utah State University

The combination of supermolecular Møller–Plesset treatment with the perturbation theory of intermolecular forces is applied in the analysis of the potential energy surface of Ar–NH3. Anisotropy of the self‐consistent field (SCF) potential is determined by the first‐order exchange repulsion. Second‐order dispersion energy, the dominating attractive contribution, is anisotropic in the reciprocal sense to the first‐order exchange, i.e., minima in one nearly coincide with maxima in the other. The estimated second‐order correlation correction to the exchange effect is nearly as large as a half ΔESCF in the minimum and has a ‘‘smoothing’’ effect on the anisotropy of ϵ(20)disp. The model which combines ΔESCF with dispersion energy (SCF+D) is not accurate enough to quantitatively describe both radial and angular dependence of interaction energy. Comparison is also made between Ar–NH3 and Ar–PH3, as well as with the Ar dimer.

  • analysis,
  • potential,
  • energy,
  • surface,
  • Ar,
  • NH3
Publication Date
January 1, 1989
Publisher Statement

Originally published by American Institute of Physics in the Journal of Chemical Physics.

Publisher's PDF can be accessed through the remote link.

Citation Information
Analysis of the potential energy surface of Ar--NH[sub 3] G. Chalasinski, S. M. Cybulski, M. M. Szczesniak, and S. Scheiner, J. Chem. Phys. 91, 7809 (1989), DOI:10.1063/1.457249