Catalytic and stoichiometric stepwise conversion of side-on bound dinitrogen to ammonia mediated by a uranium complex

The study of well-defined catalytic conversion of dinitrogen (N₂) to ammonia (NH₃) by molecular complexes is of fundamental interest and important for providing atomic-level understanding of reactivity that can be related to industrial and biological nitrogen-fixation processes. Molecular catalytic N₂ to NH₃ conversion exclusively involves reduction and protonation of terminal or bridging end-on bound metal-N₂ complexes. Thus, conspicuous by its absence is catalytic N₂ to NH₃ conversion with side-on bound metal-N₂ complexes. Here, using a uranium triamidoamine complex, we report catalytic N₂  to NH₃ conversion involving side-on bound N₂ binding. Stoichiometric reactions reveal stepwise reduction of N₂ from free-N2 to bridging side-on bound forms and subsequently to bridging nitrides, uniquely accessing four different states of side-on bound N₂ for the same molecular system. This reveals the roles of N₂, N₂^2– , N₂^3–,  N₂^4– , and N^3– in the catalytic conversion of N₂ to NH₃ when involving side-on bridging N₂.