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Multielectron reduction of diazoalkane and azides via reversible cyclometalation in ditantalum complexes
Authors:Kurogi Takashi  Ishida Yutaka  Hatanaka Tsubasa  Kawaguchi Hiroyuki
Affiliation:Department of Chemistry, Tokyo Institute of Technology, Ookayama, Meguro-ku, Tokyo 152-8551, Japan.
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.
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