首页> 外文期刊>Journal of the Korean Chemical Society >Multi-Nuclear NMR Investigation of Nickel(ll), Palladium(II), Platinum(II) and Ruthenium(II) Complexes of an Asymmetrical Ditertiary Phosphine
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Multi-Nuclear NMR Investigation of Nickel(ll), Palladium(II), Platinum(II) and Ruthenium(II) Complexes of an Asymmetrical Ditertiary Phosphine

机译:不对称二氢膦的镍(II),钯(II),铂(II)和钌(II)配合物的多核NMR研究

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摘要

Complexes synthesized by reacting alkyl and aryl phosphines with different transition metals are of great interest due to their catalytic properties. Many of the phosphine complexes are soluble in polar solvents as a result they find applications in homogeneous catalysis. In our present work we report, four transition metal complexes of Ni(II), Pd(II), Pt(II) and Ru(II) with an asymmetrical ditertiaryphosphine ligand. The synthesized ligand bears a less electronegative substituent such as methyl group on the aromatic nucleus hence makes it a strong a-donor to form stable complexes and thus could effectively used in catalytic reactions. The complexes have been completely characterized by elemental analyses, FTIR, ~1HNMR, ~(31)PNMR and FAB Mass Spectrometry methods. Based on the spectroscopic evidences it has been confirmed that Ni(II), Pd(II) and Pt(II) complexes with the ditertiaryphosphine ligand showed cis whereas the Ru(II) complex showed trans geometry in their molecular structure.
机译:通过烷基和芳基膦与不同的过渡金属反应合成的配合物由于其催化性能而引起人们的极大兴趣。许多膦配合物可溶于极性溶剂,因此它们可用于均相催化。在我们目前的工作中,我们报告了具有不对称二叔膦配体的Ni(II),Pd(II),Pt(II)和Ru(II)的四种过渡金属配合物。合成的配体在芳香核上带有较少的负电性取代基(如甲基),因此使其成为形成稳定配合物的强a-供体,因此可以有效地用于催化反应。配合物已通过元素分析,FTIR,〜1HNMR,〜(31)PNMR和FAB质谱法完全表征。基于光谱学证据,已经证实具有二叔膦配体的Ni(II),Pd(II)和Pt(II)配合物显示顺式,而Ru(II)配合物在其分子结构中显示反式几何形状。

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