31053-95-9Relevant articles and documents
PHOTODISSOCIATION OF AROMATIC THIOLS AND DISULFIDES
Borisevich, N. A.,Malkin, Ya. N.,Ruziev, Sh.,Mel'nichuk, S. V.,Tikhomirov, S. A.,et al.
, p. 468 - 471 (1990)
For the first time, the quantum yields of cleavage of SS and SH bonds in a disulfide and a thiol and also the extinction coefficient of the photoinduced aminophenylthiyl radical were determined, on the basis of which the relation of the photodissociation
Photochemical properties of excited triplet state of 6H-purine-6-thione investigated by laser flash photolysis
Alam,Fujitsuka,Watanabe,Ito
, p. 1338 - 1344 (2007/10/03)
Photochemical reactions of 6H-purine-6-thione (PuT) via the excited triplet state [3(PuT)*] have been studied by means of laser flash photolysis in organic solvents. Transient absorption bands at 475 and 690 nm were assigned to 3(PuT)*. Intersystem quantum yield and the lowest triplet energy of 3(PuT)* were evaluated to be 0.99 and 63 kcal/mol, respectively. The self-quenching rate constant is quite large (2.3×109 M-1 s-1 in THF). In photoinduced electron transfer, 3(PuT)* acts as electron acceptor for tetramethylbenzidine, while 3(PuT)* acts as electron donor for p-dinitrobenzene. Rate constants for H-atom abstraction (khT) of 3(PuT)* from benzenethiols, tocopherol, and 1,4-cyclohexadiene are on the order of 108 M-1 s-1. From the Hammett plots of khT for substituted benzenethiols, a negative ρ value indicates that 3(PuT)* has electrophilic character. In the addition reaction of 3(PuT)* toward various alkenes, the electrophilic character of 3(PuT)* was also confirmed. By steady-light photolysis of PuT, purine was produced via 3(PuT)* after H-atom abstraction. On combination of these results, the character of the lowest 3(PuT)* was presumed.
Kinetic Study for Spin-Trapping Reactions of Thiyl Radicals with Nitroso Compounds
Ito, Osamu,Matsuda, Minoru
, p. 1937 - 1940 (2007/10/02)
The rate constants for the reactions of para-substituted benzenethiyl radicals with nitroso compounds have been determined by flash photolysis.For the benzenethiyl radical the rate constants (M-1 s-1) decreased in the order pentameth