Cation assisted binding and cleavage of dinitrogen by uranium complexes

Abstract

The role of alkali promoters in N₂ cleavage by metal complexes remains poorly understood despite its relevance to the industrial production of ammonia from N₂. Here we report a series of alkali bound-oxo-bridged diuranium(III) complexes that provide a unique example of decreasing N₂ binding affinity with increasing cation size (from K to Cs). N₂ binding was found to be irreversible in the presence of K. A N₂ complex could be isolated in the solid state in the presence of the Rb cation and crystallographically characterized, but N₂ binding was found to be reversible under vacuum. In the presence of the Cs cation N₂ binding could not be detected at 1 atm. Electrochemical and Computational studies suggest that the decrease in N₂ binding affinity is due to steric rather than electronic effects. We also find that weak N₂ binding in ambient conditions does not prevent alkali assisted N₂ cleavage to nitride from occurring. More importantly, we present the first example of cesium assisted N₂ cleavage leading to the isolation of a N₂ derived multimetallic U/Cs bis-nitride. The nitrides readily react with protons and CO to yield ammonia, cyanate and cyanide.