Multielectron reduction of diazoalkane and azides via reversible cyclometalation in ditantalum complexes

Chem Commun (Camb). 2012 Jul 11;48(54):6809-11. doi: 10.1039/c2cc32535g. Epub 2012 May 31.

Abstract

Reactions of the cyclometalated hydride complexes with diazo and azide substrates are reported. While diazoalkane undergoes four-electron N-N bond cleavage, azides undergo two-electron N(2) extrusion.