Frutos María, Parvin Nasrina, Baceiredo Antoine, Madec David, Saffon-Merceron Nathalie, Branchadell Vicenç, Kato Tsuyoshi
Laboratoire Hétérochimie Fondamentale et Appliquée (UMR 5069), Université de Toulouse, CNRS, 118 route de Narbonne, F-31062, Toulouse, France.
Institut de Chimie de Toulouse (UAR 2599), Université de Toulouse, CNRS, 118 route de Narbonne, F-31062, Toulouse, France.
Angew Chem Int Ed Engl. 2022 Jul 18;61(29):e202201932. doi: 10.1002/anie.202201932. Epub 2022 May 25.
A donor-stabilized silylene 4 featuring a Ni -based donating ligand was synthesized. Complex 4 exhibits a pyramidalized and nucleophilic Si center and shows a peculiar behavior due to the cooperative reactivity of Si and Ni centers. Calculations indicate that the orientation of Ni-ligands with respect to the silylene moiety is crucial in determining the role of the Ni-fragment (Lewis acid or Lewis base) towards silylene. Indeed, a simple 90° rotation of the Si-Ni bond, reverses the role of Ni, and transforms a classical silylene→Ni complex into an unprecedented Ni →silylene complex.
合成了一种具有镍基给体配体的供体稳定硅烯4。配合物4呈现出一个金字塔形且亲核的硅中心,并由于硅和镍中心的协同反应性而表现出独特的行为。计算表明,镍配体相对于硅烯部分的取向对于确定镍片段(路易斯酸或路易斯碱)对硅烯的作用至关重要。实际上,硅-镍键简单旋转90°会使镍的作用反转,并将经典的硅烯→镍配合物转变为前所未有的镍→硅烯配合物。