The Dual Roles of Phenylenediamines: Using their Voltammetric Behavior to Measure the Hydrogen Donor and Acceptor Abilities of Alcohols in Acetonitrile.

Abstract

Cyclic voltammetry experiments on 2,3,5,6-tetramethyl-1,4-phenylenediamine (P) in acetonitrile in the presence of varying concentrations of alcohols indicate that the oxidized forms of the compound (P.+ and P2+ ) interact with the alcohols through a hydrogen-bonding mechanism where P.+ and P2+ act as the hydrogen donor and the alcohols act as acceptors. However, the neutral form (P) largely acts as a hydrogen acceptor but only for strong hydrogen donors that do not undergo proton-transfer reactions with the phenylenediamine. These results were ascertained based on measuring the difference in potential of the two one-electron transfer reactions (ΔEPox(1, 2) =|EPox(1) -EPox(2) |) in the oxidative electrochemistry of P, which thereby allows a simple measure of relative hydrogen bonding strengths.