STATE RESOLVED COLLISIONAL ENERGY TRANSFER IN HIGHLY EXCITED $NO_{2}$: STATE-TO-STATE RELAXATION, PROPENSITIES, AND COMPETITION BETWEEN BIMOLECULAR REACTION AND ENERGY TRANSFER

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1995

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Ohio State University

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A sequential optical double resonance technique with sensitive LIF-detection has been employed for the assignment and the investigation of single states of NO2 in the energy range between 17000 and 25000cm−1. Assignments for selected states and information about perturbations, "good quantum numbers", and IVR could be obtained from the double resonance spectra in the frequency domain. Subsequently, we were able to measure state-to-state rotational and vibrational energy transfer in NO2NO2 and NO2-Ar collisions, and the competition between bimolecular reaction and collisional energy transfer using a time resolved double resonance technique. From these data we obtained direct information about propensity rules and intermolecular interactions for collisional energy transfer of NO2 at high vibrational excitation

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Author Institution: Universität Göttingen, Tammannstr 6, 37077 Göttingen, Germany

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