
Journal of Chemical Physics p. 4707 - 4710 (1993)
Update date:2022-08-11
Topics:
Moralejo, C.
Cody, R. J.
Allen, J. E.
The vibrational distribution of NO(X 2?) from the reaction O(3P) + NO2(X 2A1) -> NO(X 2?,v'') + O2 was studied at room temperature in a fast-flow system.Oxygen atoms were produced via the microwave-discharge dissociation of molecular oxygen with argon as the carrier gas.The reaction time between the NO2 molecules and the oxygen atoms was kept at ca. 3 ms to minimize vibrational energy quenching.NO(X) radicals were detected via laser-induced fluorescence of the A 2Σ+ <- X 2? electronic transition.The relative vibrational population ratio of NO inthe ground electronic state was determined to be 87.4 +/- 2.6percent and 12.6 +/- 2.7percent in the v'' = 0 and v'' = 1 levels, respectively.No higher vibrational states were observed.The NO vibrational population ratio measured in this study correlates well with the earlier obervation of high vibrational excitation in O2.
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