One-electron transfer reactions of some hydroxynaphthoquinones. Solvent and substitution effect as studied by pulse radiolysis

1996 ◽  
Vol 92 (11) ◽  
pp. 1891 ◽  
Author(s):  
Madhab C. Rath ◽  
Haridas Pal ◽  
Tulsi Mukherjee
1986 ◽  
Vol 240 (3) ◽  
pp. 905-907 ◽  
Author(s):  
L G Forni ◽  
R L Willson

Absolute rate constants for the reaction of ferrocytochrome c with the thiyl radicals derived from cysteine, GSH, penicillamine and N-(2-mercaptopropionyl)glycine were measured by using the technique of pulse radiolysis. The reaction is believed to occur through a one-electron-transfer process, in agreement with the hypothesis that thiols may act as catalysts linking hydrogen-atom- and electron-transfer reactions.


Sign in / Sign up

Export Citation Format

Share Document