The vibrational predissociation of Ar–CO2 at the state-to-state level. I. Vibrational propensity rules

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Abstract
A modified version of the optothermal technique has been used to measure photofragment angular distributions resulting from the vibrational predissociation of Ar–CO2 from both members of the (1001)/(0201) Fermi diad. These angular distributions show resolvable structure which can be assigned to individual final states of the resulting fragments. The emphasis of the present paper is on the role of the vibrational degrees of freedom of the CO2 fragment as depositories for the excess energy. The dissociation energy (D0) of the complex has been determined to be 166±1 cm−1. This result is used in conjunction with the spectroscopic data already available in the literature to refine two previously reported two‐dimensional Ar–CO2 potential energy surfaces.