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Excitation of XeF* by reactions of XeF2 with Ar(3P0,2),Kr(3P2) and Xe(3P2)
Authors:J.E. Velazco  J.H. Kolts  D.W. Setser  J.A. Coxon
Affiliation:Department of Chemistry, Kansas State University, Manhattan, Kansas 66506, USA;Department of Chemistry, Dalhousie University, Halifax, Nova Scotia, Canada B3H 4J3
Abstract:The reactions of the lowest metastable states of Ar, Kr and Xe with XeF2 were studied in a flowing afterglow apparatus; XeF emission (from D2Π12 and B 2Π+ states) was observed in all cases. The total rate constants (cm3 molecule?1 s?1) for XeF* formation were determined as 75 × 10?11 ? Xe(3P2);64 × 10?11 ? Kr(3P2) and 20 × 10?11 ? Ar(3P0,2). The reactions of Ar(3P0,2) and Kr(3P2) with XeF2 also gave ArF* and KrF*, respectively. Analysis of these emissions indicates that at least two different mechanisms are operative: reactive quenching by the ionic—covalent curve-crossing mechanism and excitation transfer. The Ar(3P0,2 + XeF2 reaction is a sufficiently strong source of XeF(D—X) emission that the main features of the XeF(D2Π12 ? X2Σ+) system could be photographed and tentative assignments of these vibrational bands are given. The XeF(D → B) emission could not be observed and the ratio of the D—X versus the D—B transition probability must be > 1000 : 1.
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