
Journal of Chemical Physics p. 4033 - 4042 (1990)
Update date:2022-08-29
Topics:
Chen, Jing
Quinones, Edwin
Dagdigian, Paul J.
The H + N3 -> NH(X3Σ-, a1Δ, b1Σ+) + N2 reaction has been studied in a molecular beam-gas scattering arrangement in order to determine the nascent product state distribution.The NH product in specific rovibronic/fine-structure states has been detected by laser fluorescence excitation.The relative cross sections for formation of various vibrational levels in the a1Δ electronic state were determined to equal 1:1.0 +/- 0.3:1.4 +/- 0.3:<*>1.5 for v = 0 through 3, inclusive, while the v = 0 to v = 1 population ratio in the X3Σ- state was found to be 1:0.015 +/- 0.003.The rotational distributions in all vibronic levels were found to be characterized by temperatures near 300 K, suggestive of relaxation of the nascent rotational distributions.By comparison of the populations of a specific pair of X3Σ- and a1Δ state levels and with summation over the derived rovibrational distributions, an electronic state branching ratio of 3.2 +/- 1.3 was obtained for the X3Σ- to a 1Δ electronic state branching ratio.An upper limit of <*> 0.02 was also derived for the ratio of the b1Σ+ v = 0 to a1Δ v = 0 populations.These results are compared with NH fragment distributions observed in the photodissociation of HN3(<*>X1A') and with our expectations based on our fragmentary knowledge of HN3 potential energy surfaces.
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