Metal phthalocyanines (Fe, Co, Ni and Sn) and ruthenium tetramethylcyclam 14 and 15 were studied as cocatalysts for methanol oxidation on platinum supported catalysts. The formation of well defined monolayers of the adsorbed complexes was inferred from the Langmuirian form of the adsorption isotherms in solutions of macrocycles. The coverage at monolayer levels was low, e.g. 1.25 to 2.25 x 10(13) molecules cm(-2) or 400 to 800 Angstrom(2) molecule(-1). Enhancement for the methanol oxidation reaction was observed for Pt co-catalyzed with Sn phthalocyanine and Ru tetramethylcyclam. Ru tetramethylcyclam showed an enhancement for methanol oxidation on a per unit weight basis over pure Pt, approaching the activity of PtRu at lower potentials. Increasing the size of the nitrogen ring from 14 to 15 resulted in a lower redox potential and increase in the activity of methanol oxidation. The activity of Pt co-catalyzed with Ru TMC 15 decreased with time suggesting that the macrocycle was desorbing from the supported catalyst surface.