Photodissociation of ethyl bromide cation, C2H5Br+, as well as its isotopomers CH3CD2Br+ and CD3CH2Br+ has been studied at 355 nm by means of time of flight mass spectrometry (TOF-MS) and ion velocity imaging techniques. The TOF mass spectrum of fragment ions from C2H5Br++hν355 nm shows three peaks at m/e of 29 (C2H5+), 28 (C2H4+) and 27 (C2H3+). The TOF spectra for the two isotopomers CH3CD2Br+ and CD3CH2Br+ clearly show that all possible H-loss patterns are operative. The observation indicates that both three- and four-center intermediates are involved for both C2H4+ and C2H3+ channels. Images are recorded for C2H5+, C2H5+ + C2H4+ and C2H3+ ions, from which translational energy and angular distributions are derived using back-projection algorithm. The C2H5+ + Br channel could be well described by a parallel excitation followed by fast fragmentation with β∼1.7. C2H4++HBr channel has a very small translational energy release and a nearly isotropic angular distribution. Most of the energy went into the vibrational degrees of freedom of both C2H4+ and HBr. The anisotropy parameter β∼1.0 is found for C2H3+, whose translational energy is slightly higher than C2H4+, but much lower than C2H5+. From these results, we can rule out the possibility of the secondary dissociation of C2H5+ or C2H4+. Reaction C2H5Br++hν355 nm → C2H3++H2+Br could be considered as a concerted three-body dissociation process. Before Br atom moves out of the interaction range the H2 molecule is already formed. Morework is being done to reveal each of the H-loss channels. By measuring negative ions from C2H5Cl and CH3Br we show that the previously proposed ion-pair mechanism for the formation of C2H5+ from ethyl bromide at 118 nm is wrong [J. Phys. Chem. A 101 (1997) 1222].
Print ISSN: 0942-9352
Volume: 215, 02/2001
Pages: 253