Affiliation:
1. Department of Chemistry, Faculty of Science, Okayama University, 3-1-1 Tsushima Naka, Kita-ku, Okayama 700-8530, Japan
Abstract
Abstract
Using a competitive trapping method employing two different traps, the
trapping rates of anionic radicals (CO2
–
· and
SO3
–
·), hydroxyl, and ethyl were quantified for various
PBN- and DMPO-type traps. We have examined the characteristic effects
of substituent and external pressure on the spin trapping of anionic
radicals and compared with those of neutral radicals such as ethyl and
hydroxyl radicals. In DMPO-type traps, the effects of substituent on
trapping rates of two anionic radicals were small compared with that
of C2H5 ·. In PBN-type traps, the large effects of
substituent on trapping rates of CO2
–
· and
C2H5 · were observed. Further, the activation volumes
determined from the pressure dependence experiments for competitive
reactions show a difference in pressure behavior between the two
trapping reactions, and enable us to speculate on the reaction
mechanism of substituted PBN and DMPO traps for anionic radicals.
Subject
Physical and Theoretical Chemistry
Cited by
5 articles.
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