Jochmann Phillip, Stephan Douglas W
Department of Chemistry, University of Toronto 80 St. George Street, Toronto, Ontario M5S 3H6, Canada.
Chem Commun (Camb). 2014 Aug 7;50(61):8395-7. doi: 10.1039/c4cc03256j.
The commercially available radical TEMPO (2,2,6,6-tetramethylpiperidin-1-yloxy) reacts with [ZnCp2] (1) to yield the homoleptic compound [Zn(TEMPO)2]2 (2) through coupling of two Cp radicals. Compound 1 reacts with H2 to afford the hydride complex [Zn(μ-H)(μ(2)-η(1)-η(1)-TEMPO)]6 (3) featuring a planar Zn6H6 ring in the solid state. Preliminary data suggest that the formation of 3 proceeds via a radical mechanism.
市售的自由基TEMPO(2,2,6,6-四甲基哌啶-1-氧基)与[ZnCp2](1)反应,通过两个Cp自由基的偶联生成同配化合物[Zn(TEMPO)2]2(2)。化合物1与H2反应得到氢化物配合物[Zn(μ-H)(μ(2)-η(1)-η(1)-TEMPO)]6(3),其在固态中具有平面Zn6H6环。初步数据表明,3的形成是通过自由基机理进行的。