Jori, NadirRajeshkumar, ThayalanScopelliti, RosarioZivkovic, IvicaSienkiewicz, AndrzejMaron, LaurentMazzanti, Marinella2022-08-012022-08-012022-08-012022-07-1410.1039/d2sc02530bhttps://infoscience.epfl.ch/handle/20.500.14299/189651WOS:000828708000001The role of alkali promoters in N-2 cleavage by metal complexes remains poorly understood despite its relevance to the industrial production of ammonia from N-2. Here we report a series of alkali bound-oxo-bridged diuranium(iii) complexes that provide a unique example of decreasing N-2 binding affinity with increasing cation size (from K to Cs). N-2 binding was found to be irreversible in the presence of K. A N-2 complex could be isolated in the solid state in the presence of the Rb cation and crystallographically characterized, but N-2 binding was found to be reversible under vacuum. In the presence of the Cs cation N-2 binding could not be detected at 1 atm. Electrochemical and Computational studies suggest that the decrease in N-2 binding affinity is due to steric rather than electronic effects. We also find that weak N-2 binding in ambient conditions does not prevent alkali assisted N-2 cleavage to nitride from occurring. More importantly, we present the first example of cesium assisted N-2 cleavage leading to the isolation of a N-2 derived multimetallic U/Cs bis-nitride. The nitrides readily react with protons and CO to yield ammonia, cyanate and cyanide.Chemistry, MultidisciplinaryChemistrymultiple bond formationmultimetallic cooperativitymagnetic communicationstepwise reductionnitrideactivationammonian-2hydrogenationligandtext::journal::journal article::research article