Document Type

Article

Journal/Book Title

Journal of Chemical Physics

Publication Date

1994

Volume

101

First Page

6800

Last Page

6809

DOI

10.1063/1.468308

Abstract

The potential energy surface of the ground state He+Cl2(1Σg) is calculated by using the perturbation theory of intermolecular forces and supermolecular Møller–Plesset perturbation theory approach. The potential energy surface of the first excited triplet He+Cl2(3Πu) was evaluated using the supermolecular unrestricted Møller–Plesset perturbation theory approach. In the ground state two stable isomers are found which correspond to the linear He–Cl–Cl structure (a primary minimum, De=45.1 cm−1, Re=4.25 Å) and to the T‐shaped structure with He perpendicular to the molecular axis (a secondary minimum, De=40.8 cm−1, Re=3.5 Å). The small difference between these geometries is mainly due to the induction effect which is larger for the linear form. The results obtained for the T‐shaped minimum are in good agreement with the excitation spectroscopy experiments which observed only the T‐shaped form [Beneventi et al., J. Chem. Phys. 98, 178 (1993)]. In the lowest triplet states correlating with Cl2(3Πu), 3A′ and 3A″, the same two isomers correspond to minima. Now, however, the T‐shaped form is lower in energy. The 3A′ and 3A″ states correspond to (De,Re) of (19.9 cm−1, 3.75 Å) and (30.3 cm−1, 3.50 Å), respectively, whereas the linear form is characterized by (19.8 cm−1, 5.0 Å). The binding energy for the T form in the lower 3A″ state is in good agreement with the experimental value of Beneventi et al.

Comments

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

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