Electron Transfer through Monolayers of Mixed Long-chain Aliphatic Acids and Alcohols

Abstract

Properties of monolayers of cetyl, stearyl, and eicosyl alcohols and stearic and behenic acids and their mixtures are studied, along with the kinetics of a redox reaction of hemin adsorbed on these monolayers. Three-dimensional computer models of corresponding monolayers are constructed and compared with their electrochemical behavior. Properties of monolayers of cetyl alcohol in acid and alkaline solutions and stearyl alcohol in acid solutions correspond to package of molecules in a stretched conformation oriented normally to the electrode surface; for the other one-component systems, the monolayer structure is less regular. The hemin redox reaction rate has no correlation whatsoever with the monolayer thickness and is defined by the length of the electron transfer path (over a chain of covalent bonds and through van der Waals contacts between molecules). The stronger the deviation of the conformation of molecules from the stretched one, the shorter the effective path of the electron transfer. In mixed films of stearic acid and cetyl alcohol (1 : 6), it is sometimes possible to keep molecules of stearic acid in a stretched conformation, thus inhibiting the electron transfer along the hydrocarbon chain of this molecule to a maximum extent. The other mixed systems, while making the conformation more stretched, fail to provide for a completely regular structure.