Reduction of highly bulky triphenolamine molybdenum nitrido and chloride complexes.

Transition metal nitrides are key intermediates in the catalytic reduction of dinitrogen to ammonia. To date, transition metal nitride complexes with the triphenolamine (TPA) ligand have not been reported and the system with the ligand has been much less studied for ammonia formation compared with other systems. Herein, we report a series of molybdenum complexes supported by a sterically demanding TPA ligand, including a nitrido complex NMo(TPA). We achieved the stoichiometric conversion of the nitride moiety into ammonia under ambient conditions by adding proton and electron sources to NMo(TPA). However, the catalytic turnover for N reduction to ammonia was not observed in the triphenolamine ligand system unlike the Schrock system-triamidoamine ligand. Density functional theory calculation revealed that the molybdenum center favors binding NH over N by 16.9 kcal mol and the structural lability of the trigonal bipyramidal (TBP) molybdenum complex seems to prevent catalytic turnover. Our systematic study showed that the electronegativity and bond length of ancillary ligands determine the preference between N and NH, suggesting a systematic design strategy for improvement.