Abstract

Electronic-to-vibration (E–V) energy transfer from excited Br(4 2P1/2) atoms to nitrosyl bromide has been investigated by an infrared fluorescence technique. The excited bromine atoms are generated by pulsed laser photolysis of Br2 at 500 nm. Approximately 50% of the quenching collisions of Br*+BrNO yield BrNO molecules excited in the 1800 cm−1 v1 stretching mode. Of these, six times as many BrNO molecules are produced in the v1=1 state as in v1=2, despite the fact that the latter is nearly resonant with the electronic energy of Br*. The total rate coefficient for removal of Br* by BrNO is determined to be (1.5±0.2)×10−11 cm3 molecule−1 s−1. Indirect comparison of our results with previous work suggests that quenching proceeds primarily by inelastic collisions; reactive quenching to form Br2+NO is probably a minor channel.

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