The absorption spectra of phenazine di-N-oxide radical cation (OPO+.)
in dichloromethane were recorded by the spectroelectrochemical method
in the range from 300 to 700 nm. The reactions of the electrochemicall
y generated OPO+. with para-substituted toluenes, ethylbenzene, and cu
mene were studied. Using differential cyclic voltammetry, relative rat
e constants of reactions of OPO+. with substrates were determined; the
ir correlations with sigma(para)(+) constants of substituents gives rh
o = -2.7, which attests to the nonradical character of the reaction of
OPO+. with RH. This conclusion is confirmed by the study of the effec
t of O-2 on oxidation of ethylbenzene and cumene.