Abstract
One-electron oxidation of the rhodium(I) azido complex [Rh(N(3) )(PNP)] (5), bearing the neutral, pyridine-based PNP ligand 2,6-bis(di-tert-butylphosphinomethyl)pyridine, leads to instantaneous and selective formation of the mononuclear rhodium(I) dinitrogen complex [Rh(N(2) )(PNP)](+) (9(+) ). Interestingly, complex 5 also acts as a catalyst for electrochemical N(3)(-) oxidation (E(p) ≈-0.23 V vs. Fc(+/0) ) in the presence of excess azide. This is of potential relevance for the design of azide-based and direct ammonia fuel cells, expelling only harmless dinitrogen as an exhaust gas.