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五齿双(硫代缩氨基甲肟)锰(II)配合物的合成与光谱研究。

Synthesis and spectral investigations of Mn(II) complexes of pentadentate bis(thiosemicarbazones).

机构信息

Department of Applied Chemistry, Cochin University of Science and Technology, Kochi 682022, Kerala, India.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2010 Feb;75(2):585-8. doi: 10.1016/j.saa.2009.11.022. Epub 2009 Nov 18.

Abstract

Five Mn(II) complexes of bis(thiosemicarbazones) which are represented as [Mn(H(2)Ac4Ph)Cl(2)] (1), [Mn(Ac4Ph)H(2)O] (2), [Mn(H(2)Ac4Cy)Cl(2)].H(2)O (3), [Mn(H(2)Ac4Et)Cl(2)].3H(2)O (4) and [Mn(H(2)Ac4Et)(OAc)(2)].3H(2)O (5) have been synthesized and characterized by elemental analyses, electronic, infrared and EPR spectral techniques. In all the complexes except [Mn(Ac4Ph)H(2)O], the ligands act as pentadentate neutral molecules and coordinate to Mn(II) ion through two thione sulfur atoms, two azomethine nitrogens and the pyridine nitrogen, suggesting a heptacoordination. While in compound [Mn(Ac4Ph)H(2)O], the dianionic ligand is coordinated to the metal suggesting six coordination in this case. Magnetic studies indicate the high spin state of Mn(II). Conductivity measurements reveal their non-electrolyte nature. EPR studies indicate five g values for [Mn(Ac4Ph)H(2)O] showing zero field splitting.

摘要

五种 Mn(II) 配合物的双(硫代缩氨基甲酸盐),表示为 [Mn(H(2)Ac4Ph)Cl(2)] (1)、[Mn(Ac4Ph)H(2)O] (2)、[Mn(H(2)Ac4Cy)Cl(2)].H(2)O (3)、[Mn(H(2)Ac4Et)Cl(2)].3H(2)O (4) 和 [Mn(H(2)Ac4Et)(OAc)(2)].3H(2)O (5),已通过元素分析、电子、红外和 EPR 光谱技术进行了合成和表征。在除 [Mn(Ac4Ph)H(2)O] 之外的所有配合物中,配体作为五齿中性分子通过两个硫酮硫原子、两个亚氨基氮原子和吡啶氮原子与 Mn(II) 离子配位,表明为七配位。而在化合物 [Mn(Ac4Ph)H(2)O] 中,阴离子配体与金属配位,表明在这种情况下为六配位。磁研究表明 Mn(II) 处于高自旋态。电导率测量表明它们是非电解质性质。EPR 研究表明 [Mn(Ac4Ph)H(2)O] 有五个 g 值,显示零场分裂。

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