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首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >New Pt(II) complexes containing hemilabile thioether-pyrazole ligands. Structural analysis by H-1 C-13{H-1} and Pt-195{H-1} NMR spectroscopy and crystal structure of [PtCl(bdtp)](BPh4) [bdtp=1,5-bis(3,5-dimethyl-1-pyrazolyl)-3-thiapentane]
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New Pt(II) complexes containing hemilabile thioether-pyrazole ligands. Structural analysis by H-1 C-13{H-1} and Pt-195{H-1} NMR spectroscopy and crystal structure of [PtCl(bdtp)](BPh4) [bdtp=1,5-bis(3,5-dimethyl-1-pyrazolyl)-3-thiapentane]

机译:新型Pt(II)配合物,含有半不稳定的硫醚-吡唑配体。 H-1 C-13 {H-1}和Pt-195 {H-1} NMR谱的结构分析和[PtCl(bdtp)](BPh4)[bdtp = 1,5-bis(3,5)的晶体结构-二甲基-1-吡唑基)-3-硫杂戊烷]

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摘要

Treatment of the ligand 1,5-bis(3,5-dimethyl-l-pyrazolyl)-3-thiapentane (bdtp) with several platinum starting materials, such as K2PtCl4, PtCl2, [PtCl2(CH3CN)(2)] and [PtCl2(PhCN)(2)], have been developed under different conditions. The reactions did not yield pure products. The ratio of the NSN, NS and NN isomers has been calculated through NMR experiments. Subsequent treatment of the mixtures of complexes with NaBPh4 gave [PtCl(bdtp)](BPh4) (1). These Pt(II) complexes were characterised by elemental analysis, conductivity measurements, IR spectroscopy and H-1, C-13{H-1} and Pt-195{H-1} NMR spectroscopy. A mixture of complexes was again obtained when the complex [PtCl(bdtp)](BPh4) was heated under reflux in a solution of Et4NBr in CH2Cl2/MeOH (1:1). This proves the hemilability of the ligand bdtp with Pt(II). The X-ray crystal structure of the complex [PtCl(bdtp)](BPh4) was determined. The crystal structure contains two kinds of discrete [PtCl(bdtp)](+) cations, two BPh4- anions and two acetonitrile solvent molecules. In both cations the metal atom is tri-coordinated by the two azine nitrogen atoms and one thioether sulfur atom of the thioether-pyrazole ligand, its coordination (distorted square planar) being completed with one chlorine atom. (c) 2007 Elsevier Ltd. All rights reserved.
机译:用几种铂原料,例如K2PtCl4,PtCl2,[PtCl2(CH3CN)(2)]和[处理配体1,5-双(3,5-二甲基-1-吡唑基)-3-噻戊烷(bdtp) PtCl2(PhCN)(2)],已在不同条件下开发。反应未产生纯产物。 NSN,NS和NN异构体的比例已通过NMR实验计算得出。随后用NaBPh4处理复合物的混合物,得到[PtCl(bdtp)](BPh4)(1)。这些Pt(II)配合物通过元素分析,电导率测量,IR光谱和H-1,C-13 {H-1}和Pt-195 {H-1} NMR光谱进行表征。当将配合物[PtCl(bdtp)](BPh4)在Et4NBr的CH2Cl2 / MeOH(1:1)溶液中加热回流时,再次获得配合物混合物。这证明了配体bdtp与Pt(II)的半合性。测定了配合物[PtCl(bdtp)](BPh4)的X射线晶体结构。晶体结构包含两种离散的[PtCl(bdtp)](+)阳离子,两个BPh4-阴离子和两个乙腈溶剂分子。在两个阳离子中,金属原子被硫醚-吡唑配体的两个嗪氮原子和一个硫醚硫原子三配位,其配位(扭曲的方形平面)由一个氯原子完成。 (c)2007 Elsevier Ltd.保留所有权利。

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