MECHANISTIC STUDY OF OXIDATION REACTIONS OF HYDROQUINONE, CATECHOL, AND L-ASCORBIC-ACID BY DICYANOBIS(1,10-PHENANTHROLINE)IRON(III) IN DIMETHYL-SULFOXIDE
Hd. Takagi et al., MECHANISTIC STUDY OF OXIDATION REACTIONS OF HYDROQUINONE, CATECHOL, AND L-ASCORBIC-ACID BY DICYANOBIS(1,10-PHENANTHROLINE)IRON(III) IN DIMETHYL-SULFOXIDE, Journal of molecular liquids, 65-6, 1995, pp. 277-280
Reactions of hydroquinone, catechol, and L-ascorbic acid with dicyanob
is(1,10-phenanthroline)iron(III) were studied in dimethyl sulfoxide (D
MSO). Application of the Marcus theory to the reactions of catechol an
d hydroquinone provided the electron exchange rate constant for the Fe
(III/II) couple in DMSO. The self-exchange rate constant for the ascor
bic acid/radical couple was estimated for the first time in DMSO. The
one electron-oxidation process of L-ascorbic acid in an aprotic solven
ts such as DMSO may be completely different from that in aqueous solut
ions.