35861-33-7Relevant academic research and scientific papers
Kinetic study of the hydrogen abstraction reaction of the benzotriazole-N-oxyl radical (BTNO) with H-donor substrates
Brandi, Paolo,Galli, Carlo,Gentili, Patrizia
, p. 9521 - 9528 (2007/10/03)
The aminoxyl radical (>N-O.) BTNO (benzotriazole-N-oxyl) has been generated by the oxidation of 1-hydroxybenzotriazole (HBT; >N-OH) with a CeIV salt in MeCN. BTNO presents a broad absorption band with λmax 474 nm and e 184
Picosecond Dynamics of Nonadiabatic Proton Transfer: A Kinetic Study of Proton Transfer within the Contact Radical Ion Pair of Substituted Benzophenones/N,N-Dimethylaniline
Peters, Kevin S.,Cashin, Amanda,Timbers, Peter
, p. 107 - 113 (2007/10/03)
Picosecond absorption spectroscopy has been employed in the study of the dynamics of proton transfer within substituted benzophenones/N,N-dimethylaniline contact radical ion pairs. The reactions were investigated in the solvents cyclohexane, benzene, and dimethylformamide. The correlation of the reaction rates with the change in free energy reveals that the reaction pathway corresponds to a nonadiabatic process, that is the reaction proceeds by proton tunneling. In nonpolar solvents, an inverted region is observed in the proton-transfer process.
Direct measurement of ultrafast carbon-carbon cleavage rates via the subpicosecond charge-transfer activation of pinacols
Bockman,Hubig,Kochi
, p. 6542 - 6547 (2007/10/03)
Highly transient (benzpinacol) cation radicals (D2+.) and their ultrafast mesolytic fragmentations to the diarylhydroxymethyl radical (D.) and cation (D+) are directly observed on the early picosecond time scale upon the charge-transfer photoactivation of the intermolecular donor-acceptor complexes of pinacol donors with methyl viologen. Ultrashort lifetimes of the cation radicals with τ ~ 10 ps obtain (for the first time) from quantitative kinetics analysis of the time-resolved spectroscopic results. These rapid C-C bond scissions successfully compete with back-electron transfer, which normally predominates on this time scale, and lead to exceptionally high efficiencies for the oxidative fragmentation of pinacols.
