首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Phosphane-functionalized heavier tetrylenes: synthesis of silylene- and germylene-decorated phosphanes and their reactions with Group 10 metal complexes
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Phosphane-functionalized heavier tetrylenes: synthesis of silylene- and germylene-decorated phosphanes and their reactions with Group 10 metal complexes

机译:磷酸官能化较重的Tetrylenes:合成甲硅烷基甲硅烷和常介质装饰磷及其与10组金属配合物的反应

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摘要

The stable phosphane-functionalized heavier tetrylenes E((t)Bu(2)bzam)pyrmP(t)Bu(2)(E = Si (1(Si)), Ge (1(Ge));(t)Bu(2)bzam =N,N '-ditertbutylbenzamidinate; HpyrmP(t)Bu(2)= ditertbutyl(2-pyrrolylmethyl)phosphane) have been prepared by reacting the amidinatotetrylenes E((t)Bu(2)bzam)Cl (E = Si, Ge) with LipyrmP(t)Bu(2). The reactions of1(Si)and1(Ge)with selected M(0)and M-II(M = Ni, Pd, Pt) metal precursors have allowed the synthesis of square-planar [MCl2{kappa E-2,P-E((t)Bu(2)bzam)pyrmP(t)Bu(2)}] (M = Ni, Pd, Pt; E = Si, Ge), tetrahedral [Ni{kappa E-2,P-E((t)Bu(2)bzam)pyrmP(t)Bu(2)}(cod)] (E = Si, Ge; cod = 1,5-cyclooctadiene) and triangular [M{kappa E-2,P-E((t)Bu(2)bzam)pyrmP(t)Bu(2)}(PPh3)] (M = Pd, Pt; E = Si, Ge) complexes, showing that1(Si)and1(Ge)are excellentSi,P- andGe,P-chelating ligands that, due to their large steric bulk, are able to stabilize three-coordinate Pd(0)and Pt(0)complexes.
机译:稳定的磷酸官能化较重的Tetrylenese((t)bu(2)bzam)PyrMP(T)Bu(2)(E = Si(1(Si)),Ge(1(Ge));(t)bu( 2)BZAM = N,N' - 二苯乙烯基苯并甲酰酰胺;通过使酰胺蛋白酶丙酮醇E((T)BU(2)BZAM)Cl(E =)反应制备二酯(2-吡咯基甲基)膦酸酯(2-吡咯基甲基)膦。 Si,Ge)具有Lipyrmp(t)bu(2)。 用所选M(0)和M-II(M = Ni,Pd,Pd)金属前体的1(Si)和1(Ge)的反应允许合成方形平面[Mcl 2 {kappa e-2,pe(( t)Bu(2)Bzam)PyrMP(T)Bu(2)}](M = Ni,Pd,Pt; e = Si,Ge),四面体[Ni {kappa e-2,Pe((t)bu( 2)Bzam)PyrMP(T)Bu(2)}(COD)](e = Si,Ge; Cod = 1,5-环辛二烯)和三角形[M {kappa E-2,PE((T)BU(2 )Bzam)PyrMP(T)Bu(2)}(PPH3)](M = Pd,Pt; e = Si,Ge)复合物,显示该1(Si)和1(GE)是卓越的,P-Andge,P-Chelating 由于它们的大型块状物,能够稳定三坐标Pd(0)和Pt(0)络合物的配体。

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