ISSN:
1089-7690
Quelle:
AIP Digital Archive
Thema:
Physik
,
Chemie und Pharmazie
Notizen:
This paper presents product translational energy spectroscopy measurements of the primary photofragmentation channels of 2-chloropropene excited at 193 nm and of the unimolecular dissociation of the 2-propenyl radical. Tunable vacuum ultraviolet (VUV) photoionization of the products allows us to distinguish between the various product isomers formed in these processes. The data show evidence for three significant primary reaction channels in the dissociation of 2-chloropropene: An excited-state C–Cl fission channel producing fast Cl atoms, a C–Cl fission channel producing slow Cl atoms, and HCl elimination. A minor C–CH3 fission channel contributes as well. The measured branching of the major primary product channels is: [fast C–Cl]:[slow C–Cl]:[HCl elimination]=62%:23%:15%. The experiments also allow us to resolve selectively the product branching between the unimolecular dissociation channels of the 2-propenyl radical, a high energy C3H5 isomer; we measure how the branching ratio between the two competing C–H fission channels changes as a function of the radical's internal energy. The data resolve the competition between the unimolecular H+allene and H+propyne product channels from the radical with internal energies from 0 to 18 kcal/mol above the H+propyne barrier. We find that the barrier to H+allene formation from this high-energy C3H5 radical is higher than the barrier to H+propyne formation, in agreement with recent theoretical calculations but in sharp contrast to that predicted for the most stable C3H5 isomer, the allyl radical. The experiments demonstrate a general technique for selectively forming a particular CnHm isomer dispersed by internal energy due to the primary photolysis, thus allowing us to determine the branching between unimolecular dissociation channels as a function of the selected radical isomer's internal energy. © 2001 American Institute of Physics.
Materialart:
Digitale Medien
URL:
http://dx.doi.org/10.1063/1.1345877
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