Abstract
AbstractCatalytic formation of borylamines from atmospheric N2 is achieved for the first time using a series of homogenous (triphosphine)Mo complexes. Stepwise functionalization of the (triphosphine)Mo‐nitrido complex with chloroborane led to the synthesis of the imido complex. Electrochemical characterization of the (PPP)Mo‐nitrido and (PPP)Mo‐borylimido complexes showed that the latter is much more easily reduced.
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