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首页> 外文期刊>Acta crystallographica. Section C, Structural chemistry. >Caesium bis(5-bromosalicylaldehyde thiosemicarbazonato-kappa~3O,N,S)-ferrate(III): supramolecular arrangement of low-spin FeIII complex anions mediated by Cs~+ cations
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Caesium bis(5-bromosalicylaldehyde thiosemicarbazonato-kappa~3O,N,S)-ferrate(III): supramolecular arrangement of low-spin FeIII complex anions mediated by Cs~+ cations

机译:双(5-溴水杨醛硫代半碳氮杂--3O,N,S)-高铁酸铯(III):Cs〜+阳离子介导的低旋转FeIII络合物阴离子的超分子排列

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摘要

The synthesis and crystal structure determination (at 293 K) of the title complex, Cs[Fe(C_8H_6BrN_3OS)_2], are reported. The compound is composed of two dianionic O,N,S-tridentate 5-bromosalicylaldehyde thiosemicarbazonate(2-) ligands coordinated to an FeIII cation, displaying a distorted octahedral geometry. The ligands are orientated in two perpendicular planes, with the O- and S-donor atoms in cis positions and the N-donor atoms in trans positions. The complex displays intermolecular N-H...O and N-H...Br hydrogen bonds, creating R44(18) rings, which link the FeIII units in the a and b directions. The FeIII cation is in the low-spin state at 293 K.
机译:报告了标题化合物Cs [Fe(C_8H_6BrN_3OS)_2]的合成和晶体结构测定(在293 K)。该化合物由与FeIII阳离子配位的两个阴离子二价O,N,S-三齿5-溴水杨醛硫代半氨基甲酸(2-)配体组成,显示出扭曲的八面体几何形状。配体在两个垂直平面中取向,O-和S-供体原子位于顺式位置,N-供体原子处于反式位置。该复合物显示分子间的N-H ... O和N-H ... Br氢键,形成R44(18)环,该环在a和b方向上连接FeIII单元。 FeIII阳离子在293 K处于低自旋状态。

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