Ammonia Activation, H2 Evolution and Nitride Formation from a Molybdenum Complex with a Chemically and Redox Noninnocent Ligand

Treatment of the bis­(imino)­pyridine molybdenum η6-benzene complex (iPrPDI)­Mo­(η6-C6H6) (iPrPDI, 2,6-(2,6-iPr2C6H3NCMe)2C5H3N) with NH3 resulted in coordination induced haptotropic rearrangement of the arene to form (iPrPDI)­Mo­(NH3)2(η2-C6H6). Analogous η2-ethylene and η2-cyclohexene complexes were also synthesized, and the latter was crystallographically characterized. All three compounds undergo loss of the η2-coordinated ligand followed by N–H bond activation, bis­(imino)­pyridine modification, and H2 loss. A dual ammonia activation approach has been discovered whereby reversible M–L cooperativity and coordination induced bond weakening likely contribute to dihydrogen formation. Significantly, the weakened N–H bonds in (iPrPDI)­Mo­(NH3)2(η2-C2H4) enabled hydrogen atom abstraction and synthesis of a terminal nitride from coordinated ammonia, a key step in NH3 oxidation.