Dissociative photoionization of CH 3C(O)CH 2 to C 2H 5+

Abstract

We use a combination of crossed laser-molecular beam scattering experiments and velocity map imaging experiments to investigate the dissociative ionization of the CH 3C(O)CH 2 radical to C 2H 5 +. We form the radical from C–Cl bond fission in the photodissociation of chloroacetone at 193 nm. Upon 10.5 eV VUV photoionization, the radical is not detected at a parent mass-to-charge ratio of 57, but instead is only detected at the fragment m/ z = 29 (C 2H 5 +). While the appearance of multiple daughter ions is expected, and indeed observed, using 200 eV electron bombardment ionization, one normally expects “soft” VUV photoionization to give signal at parent ion. We present electronic structure calculations that offer an explanation of our experimental results. The results presented herein also confirm the presence of a minor dissociation channel for the highly vibrationally excited CH 3C(O)CH 2 radicals – one that forms C 2H 5 + CO following isomerization to CH 3CH 2CO.