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Pd(II) 和 Ni(II) 配合物的“膦亚胺”配体:合成与密度泛函理论研究。

Pd(II) and Ni(II) complexes featuring a "phosphasalen" ligand: synthesis and DFT study.

机构信息

Laboratoire Hétéroéléments et Coordination, Ecole Polytechnique, CNRS, 91128, Palaiseau Cedex, France.

出版信息

Dalton Trans. 2011 Oct 21;40(39):10029-37. doi: 10.1039/c1dt10906e. Epub 2011 Aug 30.

Abstract

A phosphorus analog of salen ligands featuring iminophosphorane functionalities in place of the imine groups was synthesised in 2 steps from o-diphenylphosphinophenol via the preparation of the corresponding bis-aminophosphonium salt. This novel tetradentate ligand (1), which we named phosphasalen, was coordinated to Pd(II) and Ni(II) metal centres affording complexes 6 and 7 respectively, which were characterised by multinuclear NMR, elemental and X-ray diffraction analyses. Both neutral complexes adopt a nearly square-planar geometry around the metal with coordination of all iminophosphorane and phenolate moieties. The electronic properties of these new complexes were investigated by cyclic voltammetry and comparison with known salens was made when possible. Moreover, the particular behaviour of the phosphasalen nickel complex 7 was further investigated through magnetic moment measurements and a DFT study.

摘要

合成了一种磷类似物的 salen 配体,其中亚氨基膦烷官能团取代了亚胺基团。该配体通过邻二苯膦酚合成,分两步进行,首先制备相应的双氨基磷盐。这种新型四齿配体(1),我们命名为磷-salen,与 Pd(II) 和 Ni(II) 金属中心配位,分别得到配合物 6 和 7,通过多核 NMR、元素和 X 射线衍射分析对其进行了表征。两个中性配合物在金属周围采用几乎正方形平面几何形状,其中所有亚氨基膦烷和苯氧基团都进行了配位。通过循环伏安法研究了这些新配合物的电子性质,并在可能的情况下与已知的 salens 进行了比较。此外,通过磁矩测量和 DFT 研究进一步研究了磷-salen 镍配合物 7 的特殊行为。

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