Pt(1,2-bis(diethylphosphino)ethane)(PEt3)2 、 bis(2-silylphenyl)silane 以
not given 为溶剂,
生成 [Pt(depe)(H)(SiH2C6H4SiHC6H4SiH2)]
参考文献:
名称:
Reaction of [2-(SiH3)C6H4]2SiH2 with Ni(Et2PCH2CH2PEt2)(PEt3)2: Characterization of η2-(Si−H)Ni and NiIV−H Complexes
摘要:
The reaction of (2-SiH3C6H4)2SiH2 with Ni(Et2PCH2CH2PEt2)(PEt3)2 afforded a new silylnickel complex, which, in the solid state, was determined to be a bis(silyl)eta2-(Si-H)nickel complex, the first example of eta2-(Si-H)nickel complex by single-crystal X-ray analysis. Variable-temperature NMR spectroscopy revealed fluxional behavior of the complex in solution; at room temperature, exchange of five hydrogens (two SiH2 and one hydrogen bound to nickel) was observed, while at -80 degrees C the exchange of hydrogens appeared frozen to adopt a tris(silyl)(hydrido)nickel(IV) structure, which was confirmed by theoretical calculation. The latter complex is the first example of hydridonickel(IV) complex.
R2PCH2CH2PR2 (R = Me or Et) to give dinuclear (silyl)(µ-silylene)palladium(II) complexes, while the reaction with a mixture of Pd(Pet3)4 and Cy2PCH2CH2Pcy2 (Cy = cyclohexyl) afforded a mononuclear (silyl)(disilanyl)palladium(II) complex, the Si–Si bond of which was formed by the intramolecular dehydrocoupling. The structures of the new complexes were determined by X-ray diffraction.
一种新的三齿氢硅烷 (2-SiH3C6H4)2SiH2 与 Pd(Pet3)4 和 R2PCH2CH2PR2(R = Me 或 Et)的混合物反应生成双核(甲硅烷基)(μ-亚甲硅烷基)钯(II)配合物,同时与Pd(Pet3)4 和 Cy2PCH2CH2Pcy2(Cy = 环己基)的混合物提供了单核(甲硅烷基)(二硅烷基)钯(II)配合物,其 Si-Si 键是通过分子内脱氢偶联形成的。新配合物的结构由 X 射线衍射确定。
Reaction of [2-(SiH<sub>3</sub>)C<sub>6</sub>H<sub>4</sub>]<sub>2</sub>SiH<sub>2</sub> with Ni(Et<sub>2</sub>PCH<sub>2</sub>CH<sub>2</sub>PEt<sub>2</sub>)(PEt<sub>3</sub>)<sub>2</sub>: Characterization of η<sup>2</sup>-(Si−H)Ni and Ni<sup>IV</sup>−H Complexes
The reaction of (2-SiH3C6H4)2SiH2 with Ni(Et2PCH2CH2PEt2)(PEt3)2 afforded a new silylnickel complex, which, in the solid state, was determined to be a bis(silyl)eta2-(Si-H)nickel complex, the first example of eta2-(Si-H)nickel complex by single-crystal X-ray analysis. Variable-temperature NMR spectroscopy revealed fluxional behavior of the complex in solution; at room temperature, exchange of five hydrogens (two SiH2 and one hydrogen bound to nickel) was observed, while at -80 degrees C the exchange of hydrogens appeared frozen to adopt a tris(silyl)(hydrido)nickel(IV) structure, which was confirmed by theoretical calculation. The latter complex is the first example of hydridonickel(IV) complex.