首页> 外文期刊>Inorganica Chimica Acta >Concentration-dependent palladium(II)-indole bond formation in complexes with a 2N-donor ligand containing an indole moiety: Synthesis, characterization, and reaction analysis
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Concentration-dependent palladium(II)-indole bond formation in complexes with a 2N-donor ligand containing an indole moiety: Synthesis, characterization, and reaction analysis

机译:与含吲哚部分的2N供体配体配合物中浓度依赖的钯(II)-吲哚键形成:合成,表征和反应分析

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摘要

The Pd(II) complexes of a 2N-donor ligand containing a pendent indole, 3-(2-pyridylmethylamino)ethylindole (L), were synthesized and characterized. Reaction of the ligand with [PdCl_2(CH_3CN)_2] at room temperature gave [Pd(L)Cl_2] (1) as pale yellow crystals. The X-ray crystal structure analysis and 1H NMR spectrum of 1 revealed that the complex has a 2N2Cl-donor set in a square-planar geometry and that the pendent indole ring has no characteristic intramolecular interaction with the Pd(II) ion and the coordinated pyridine moiety. Refluxing a solution of 1 in CH_2Cl_2/DMF for a few hours under basic conditions gave yellow crystals, which were shown to be an indole-C2 binding complex [Pd(L)Cl] (2) by X-ray analysis. Conversion of complex 1 to 2 in DMSO was observed upon dilution of the solution of complex 1. From solution equilibrium and kinetic studies the initial step of the conversion by dilution has been assigned to the replacement of a coordinated Cl- ion with the DMSO molecule. The ligand replacement easily occurred at low concentrations of 1. The complex with a coordinated solvent molecule exhibited a high reactivity and formed a stable Pd-C bond with the indole ring located close to the Pd(II) center. We discussed the concentration dependent formation of the indole-C2 binding complex 2 and its detailed mechanism.
机译:合成并表征了包含侧基吲哚3-(2-吡啶基甲基氨基)乙基吲哚(L)的2N供体配体的Pd(II)配合物。所述配体与[PdCl_2(CH_3CN)_2]在室温下反应,得到[Pd(L)Cl_2](1),为浅黄色晶体。 X射线晶体结构分析和1H NMR谱图表明,该配合物具有2N2Cl供体,其设置为正方形平面几何形状,而悬垂的吲哚环与Pd(II)离子和配位化合物之间没有分子内相互作用吡啶部分。在碱性条件下,将1在CH_2Cl_2 / DMF中的溶液回流数小时,得到黄色晶体,通过X射线分析显示其为吲哚-C2结合复合物[Pd(L)Cl](2)。稀释复合物1的溶液后,观察到DMSO中复合物1向2的转化。从溶液平衡和动力学研究出发,通过稀释转化的初始步骤已被指定为用DMSO分子取代配位的Cl-离子。在低浓度1时容易发生配体置换。具有配位溶剂分子的配合物表现出高反应活性,并与靠近Pd(II)中心的吲哚环形成稳定的Pd-C键。我们讨论了浓度依赖性的吲哚-C2结合复合物2的形成及其详细的机制。

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