Hydrogenation of a Trinuclear μ3‐Imido Complex of Ruthenium: Homolytic or Heterolytic H–H Bond Cleavage?
Hajime Kameo, Yumiko Nakajima, Hiroharu Suzuki
Abstract
Hajime Kameo, Yumiko Nakajima, Hiroharu Suzuki
Abstract
Abstract To elucidate the mode of hydrogen–hydrogen bond cleavage at transition metal sites that cooperate with a heteroatom, the hydrogenation of trinuclear μ3‐imido complex (Cp*Ru)3(μ3‐NH)(μ‐H)3 (Cp* = η5‐C5Me5) (1) with deuterium was carried out. The percentage of deuterium content in the amido ligand of (Cp*Ru)3(μ‐NH2)(μ‐H)4 (2), which was generated as an intermediate in the reaction of 1 with dihydrogen, proved that hydrogenation of 1 to 2 proceeded through homolytic cleavage of dihydrogen.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)
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Abstract To elucidate the mode of hydrogen–hydrogen bond cleavage at transition metal sites that cooperate with a heteroatom, the hydrogenation of trinuclear μ3‐imido complex (Cp*Ru)3(μ3‐NH)(μ‐H)3 (Cp* = η5‐C5Me5) (1) with deuterium was carried out. The percentage of deuterium content in the amido ligand of (Cp*Ru)3(μ‐NH2)(μ‐H)4 (2), which was generated as an intermediate in the reaction of 1 with dihydrogen, proved that hydrogenation of 1 to 2 proceeded through homolytic cleavage of dihydrogen.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)
Key concepts: Heterolysis, Chemistry, Homolysis, Bond cleavage, Ruthenium, Deuterium, Heteroatom, Cleavage (geology)