Electrochemical study of some 2,5-dimethoxyamphetamine derivatives
A set of 2,5-dimethoxyamphetarnines differing in their substitution at C4 was studied by differential pulse voltammetry and linear scan cyclic voltammetry in aqueous media. These experiments showed a single oxydation peak for each of the compounds studied. This peak is attributed to oxidation of the aromatic ring with formation of a radical cation stabilized by the methoxy group bonded to the benzene ring.
This work was supported in part by FONDECYT Grants N 1120-92 and 915-89 and DTI grants N Q 3121-9013.
Quote ItemJournal of Chemical Physics, Vol. 89, pp. 669-679, 1992.