ISOMERS IN HELIUM COMPLEXES: OBSERVATION OF T-SHAPED AND LINEAR $He-CH_{3}F$, AND PREDICTION OF TWO NEARLY ISOENERGETIC FORMS OF $He-ClF_{3}$

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2000

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Ohio State University

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The existence of multiple minima on the intermolecular potential energy surface of rare gas-molecule complexes appears quite general. Localization of the rare gas atom in the various potential energy minima results in several ``isomeric'' forms of a single complex. The combination of ab initio calculations and microwave/millimeter wave spectroscopy of helium-molecule complexes has proven quite valuable in the study of this phenomena. As presented $previously.^{a}$ the ab initio intermolecular potential of $He-CH_{3}F$ exhibits two main wells: $-46.9 cm^{-1}$ in the ``linear'' position at the C end of the C-F axis, and $-44.8 cm^{-1}$ in the ``T-shaped'' position on the side of the C-F axis. Bound state calculations place the ground state in the T-shaped position with a state localized in the linear position being $4.0 cm^{-1}$ higher in energy. Pure rational transitions of states localized in the each minima, as well as transitions between the states, have now been observed experimentally. The initial observation of the linear state depended upon strong mixing of the $J_{K_{a}}K_{c} = 2_{20}$ level of the ground state with the $J_{K}=2_{0}$ level of the linear state. This mixing is accurately is accurately predicated by the ab initio potential and serves as a sensitive probe of the intermolecular potential. The observed T-shaped to linear gap is $4.4 cm^{-1}$. The intermolecular potential of $He-ClF_{3}$ at the MP2 level was previously $presented.^{b}$ While qualitatively correct, significant quantitative differences existed between the MP2 surface and selected points calculated at the MP4 level. We report a much refined full MP4 surface and bound state calculations. Two primary minima exist: $-53.9 cm^{-1}$ in the linear position at the Cl end of the $C_{2e}$ axis, and $-59.9 cm^{-1}$ in the T-shaped position above the molecular plane. Bound state calculation places the ground state in the linear minima, with a T-shaped state less than 1 GHz higher in energy. It is interesting to note that in both $He-ClF_{3}$ and $He-CH_{3}F$ the ground state is localized in the shallower of the two potential minima.

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$^{a}$54th International Symposium on Molecular Spectroscopy (1999) $^{b}$52nd International Symposium on Molecular Spectroscopy (1997)
Author Institution: Department of Chemistry and Chemical Biology, Harward University

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