Catalytic Formation of Ammonia from Molecular Dinitrogen by Use of Dinitrogen-Bridged Dimolybdenum–Dinitrogen Complexes Bearing PNP-Pincer Ligands: Remarkable Effect of Substituent at PNP-Pincer Ligand

A series of dinitrogen-bridged dimolybdenum–dinitrogen
complexes
bearing 4-substituted PNP-pincer ligands are synthesized by the reduction
of the corresponding molybdenum trichloride complexes under 1 atm
of molecular dinitrogen. In accordance with a theoretical study, the
catalytic activity is enhanced by the introduction of an electron-donating
group to the pyridine ring of PNP-pincer ligand, and the complex bearing
4-methoxy-substituted PNP-pincer ligands is found to work as the most
effective catalyst, where 52 equiv of ammonia are produced based on
the catalyst (26 equiv of ammonia based on each molybdenum atom of
the catalyst), together with molecular dihydrogen as a side-product.
Time profiles for the catalytic reactions indicate that the rates
of the formation of ammonia and molecular dihydrogen depend on the
nature of the substituent on the PNP-pincer ligand of the complexes.
The formation of ammonia and molecular dihydrogen is complementary
in the reaction system.