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Title: Br{sub 2} molecular elimination in 248 nm photolysis of CHBr{sub 2}Cl by using cavity ring-down absorption spectroscopy

Journal Article · · Journal of Chemical Physics
DOI:https://doi.org/10.1063/1.2426334· OSTI ID:20868216
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  1. Department of Chemistry, National Taiwan University, Taipei 106, Taiwan and Institute of Atomic and Molecular Sciences, Academia Sinica, Taipei 106, Taiwan (China)

Elimination of molecular bromine is probed in the B {sup 3}{pi}{sub ou}{sup +}<-X {sup 1}{sigma}{sub g}{sup +} transition following photodissociation of CHBr{sub 2}Cl at 248 nm by using cavity ring-down absorption spectroscopy. The quantum yield for the Br{sub 2} elimination reaction is determined to be 0.05{+-}0.03. The nascent vibrational population ratio of Br{sub 2}(v=1)/Br{sub 2}(v=0) is obtained to be 0.5{+-}0.2. A supersonic beam of CHBr{sub 2}Cl is similarly photofragmented and the resulting Br atoms are monitored with a velocity map ion-imaging detection, yielding spatial anisotropy parameters of 1.5 and 1.1 with photolyzing wavelengths of 234 and 267 nm, respectively. The results justify that the excited state promoted by 248 nm should have an A{sup ''} symmetry. Nevertheless, when CHBr{sub 2}Cl is prepared in a supersonic molecular beam under a cold temperature, photofragmentation gives no Br{sub 2} detectable in a time-of-flight mass spectrometer. A plausible pathway via internal conversion is proposed with the aid of ab initio potential energy calculations. Temperature dependence measurements lend support to the proposed pathway. The production rates of Br{sub 2} between CHBr{sub 2}Cl and CH{sub 2}Br{sub 2} are also compared to examine the chlorine-substituted effect.

OSTI ID:
20868216
Journal Information:
Journal of Chemical Physics, Vol. 126, Issue 3; Other Information: DOI: 10.1063/1.2426334; (c) 2007 American Institute of Physics; Country of input: International Atomic Energy Agency (IAEA); ISSN 0021-9606
Country of Publication:
United States
Language:
English