4.6 Article

Rate coefficients for rotational energy transfer from the levels OH(X 2Π3/2, v=1, ji=1.5, 3.5-8.5) in collisions with He, Ar, N2 and HNO3

Journal

PHYSICAL CHEMISTRY CHEMICAL PHYSICS
Volume 4, Issue 22, Pages 5613-5621

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/b207549k

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Using an infrared-ultraviolet double resonance method, we have measured rate coefficients at room temperature for the transfer of OH radicals from rotational levels between j(i) = 1.5 (N = 1) and j(i) = 8.5 (N = 8) in the X (2)Pi, Omega = 3/2; nu = 1 vibronic state in collisions with He, Ar, N(2) and HNO(3) . OH radicals were generated by 266 urn pulsed laser photolysis of HNO(3) and promoted to selected ji using a pulsed infrared laser tuned to an appropriate line in the (1,0) infrared fundamental band of OH. The evolution of population in selected levels was observed using time-delayed laser-induced fluorescence in the (1,1) band of the A (2)Sigma(+)-X (2)Pi system. The results of two kinds of measurement are reported. For j(i) = 3.5 and 6.5, a single Lambda-doublet component of the selected rotational level was excited and the evolution of the populations in both Lambda-doublet components was observed. The decay of the sum of the two individual populations then yields rate coefficients for the transfer of population from j(i), free of complications arising from the transfer of population between the two Lambda-doublet levels. For a wider range of levels, including j(i) = 6.5, we have carried out simpler measurements in which rate coefficients for transfer from the initially excited level j(i) are inferred by monitoring only the change in population in the Lambda-doublet level that is directly populated by the pump laser. Measurements of both kinds have been carried out for j(i) = 6.5 and the rate coefficients derived from the two sets of measurements are in good agreement. The measured rate coefficients for rotational relaxation (k(RET)) show a significant dependence on both the collision partner, with k(RET)(He)approximate tok(RET)(Ar) < k(RET)(N(2)) < k(RET)(HNO(3)), and on the rotational level with the values of k(RET) generally decreasing as j(i) is increased beyond j(i) = 3.5.

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