On irradiation in solution in hydrogen-donating solvents, methyl and ethyl pyruvale react through their excited singlet and triplet states to yield a pair of isomeric radicals. Each isomer is formed via both pathways, but in some solvents one is produced predominantly from the singlet state and the
CIDEP study of the formation of a cyclohexadienyl-type radical in the hydrogen abstraction reactions of triplet xanthone
β Scribed by Yoshio Sakaguchi; Hisaharu Hayashi; Hisao Murai; J. I'haya; Kunio Mochida
- Publisher
- Elsevier Science
- Year
- 1985
- Tongue
- English
- Weight
- 357 KB
- Volume
- 120
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
From CIDEP measuremen& a new reaction or ~nplr~ xnnthone hydrogen abswwuon by a benzene rmg was found IO occur in the reactions wllh nethylgermane and sodurn borohldnds An anomalous E/A phase pa1k.m wIthIn each h>pfrfine lme WLB also obsened for the generated cyclohexadlenyl-type radical in a mnzelle
π SIMILAR VOLUMES
Rate consfanis for the reactions of the hydroxyc~clohexodienyl ( E:CMD) radical. the adduct of the OH + benzene reaction, with NO, (1 J and NO (2) in rhe gas phase have been delermined ar 298 K using long-path cw UV laser absorplion LO monitor HCHD. The rate cons~anu are Found 10 be k, = (8.5~2.1)~1
Chemically induced dynamic electron polarization (CIDEP) generated through the interaction of the excited triplet state of benzophenone with the 2,2,6,6,-tetramethyl-l-piperidinyloxyl (TEMPO) radical was investigated by time-resolved ESR spectroscopy in benzene solution. We carefully examined what f
## Abstract By means of the dualβlevel direct dynamics method, the mechanisms of the reactions, CH~3~CF~2~Cl + OH β products (R1) and CH~3~CFCl~2~ + OH β products (R2), are studied over a wide temperature range 200β2000 K. The optimized geometries and frequencies of the stationary points are calcul