The products of the reactions of electronically excited Ar(3P0,3P2), Kr(3P2), and Xe(3P2) atoms with the chloromethanes, chlorofluoromethanes, CF3H, CF2HCl, CFHCl2, CF2Clsdot;CF2Cl, CF3sdot;CCl3, and HCl have been investigated by the dischargehyphen;flow technique, using atomic resonance fluorescence to probe dissociation channels and emission spectroscopy. Energy transfer leading to cleavage of Cndash;H or Cndash;Cl bonds is extremely efficient, particularly in the reactions of Xe(3P2) with CF2Cl2and CFCl3and of Ar(3P0,thinsp;2) with CFCl3, in which more than two Cl atoms are released per primary reactive event. The observation of contrasting behavior in the reactions of Xe(3P2) with CF3H and CF4has led to the discovery of a qualitative correlation between the rate constants, the products of the energy transfer process, and the accessibility of dissociative or ionizing states of the reagent molecule, as revealed by its vacuum UV absorption spectrum.
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