Drastic acceleration of hexacyanoferrate(II) oxidation in the presence of strong electron-donor solvents
Abstract
The rate of oxidation of [Fe(CN)6]4– to [Fe(CN)6]3– by O2 in aqueous–organic solvent mixtures depends drastically on the electron-donating abilites of the solvents, the reaction in dimethyl sulphoxide and dimethylformamide being about 104 times faster than in water; the rate does not correlate with the solvent's dielectric constant.