Radiation chemistry of organic molecules in solid rare gas matrices: 2. Selective deprotonation of the primary radical cations upon irradiation of oxygen-containing molecules in xenon matrices

Citation
Vi. Feldman et al., Radiation chemistry of organic molecules in solid rare gas matrices: 2. Selective deprotonation of the primary radical cations upon irradiation of oxygen-containing molecules in xenon matrices, HIGH ENERG, 35(5), 2001, pp. 319-327
Citations number
36
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
HIGH ENERGY CHEMISTRY
ISSN journal
00181439 → ACNP
Volume
35
Issue
5
Year of publication
2001
Pages
319 - 327
Database
ISI
SICI code
0018-1439(200109/10)35:5<319:RCOOMI>2.0.ZU;2-O
Abstract
The composition of radical products trapped after irradiation of various et hers (dimethyl ether, tetrahydrofuran, methylal, 1,3-dioxolane) or acetalde hyde in xenon matrices at 15-17 K in the presence of electron scavengers wa s studied by an ESR technique. It was shown that the primary radical cation s give corresponding deprotonation products (carbon-centered radicals), rat her than stabilize in xenon, under the given experimental conditions. The d eprotonation process is characterized by extremely high selectivity; i.e., the only type of radicals resulting from deprotonation at maximum spin dens ity position was observed in each of the cases. The possible mechanism of t he reactions and the nature of their selectivity are discussed.