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Catalytic Dinitrogen Reduction at the Molybdenum Center Promoted by a Bulky Tetradentate Phosphine Ligand
Author(s) -
Liao Qian,
SaffonMerceron Nathalie,
Mézailles Nicolas
Publication year - 2014
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.201408664
Subject(s) - phosphine , chemistry , molybdenum , catalysis , trimethylsilyl , ligand (biochemistry) , stoichiometry , medicinal chemistry , center (category theory) , polymer chemistry , inorganic chemistry , crystallography , organic chemistry , receptor , biochemistry
Stoichiometric reduction of N 2 at a Mo center stabilized by a bulky tetradentate phosphine ligand ( ${{\rm PP}{{{\rm Cy}\hfill \atop 3\hfill}}}$ ) allowed isolation of Mo–imidoamine and Mo–imido complexes. Both complexes as well as the Mo II precursor are equally suitable catalysts for the synthesis of NTMS 3 (TMS=trimethylsilyl) from N 2 , TMSCl, and electron sources. Mechanistic studies prove the involvement of a TMS radical at least in one of the catalytic steps.

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