Home A Mixed Valent Thioantimonate(III,V): [SbS3]3– and [SbS4]3– as bidentate ligands: Solvothermal synthesis and crystal structure of {Mn(dien)2}2[MnSb2S7]
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A Mixed Valent Thioantimonate(III,V): [SbS3]3– and [SbS4]3– as bidentate ligands: Solvothermal synthesis and crystal structure of {Mn(dien)2}2[MnSb2S7]

  • Nicola Herzberg , Christian Näther and Wolfgang Bensch
Published/Copyright: July 16, 2012

Abstract

The new compound {Mn(dien)2}2[MnSb2S7] (dien = diethylenetriamine) was obtained under solvothermal conditions and crystallizes in the orthorhombic space group Pbca. The main structural motif is the [MnSb2S7]4– anion being constructed by a [MnS4]6– tetrahedron, a [SbIIIS3]3– and a [SbVS4]3– anion. Each thioantimonate anion shares one edge with the Mn2+ centered cation generating the [MnSb2S7]4– unit. The two independent Mn2+ cations in the two {Mn(dien)2}2+ complexes are in a distorted octahedral environment of two tridentate acting dien molecules. One cation displays the λδλλ-conformation and the other the δλλδ-conformation. Several intermolecular S···H—N bonding interactions are found between the cations and the anions.


* Correspondence address: Christian-Albrechts-Universität zu Kiel, Institut für Anorganische Chemie, Max-Eyth-Str. 2, 24118 Kiel, Deutschland,

Published Online: 2012-07-16
Published in Print: 2012-08

© by Oldenbourg Wissenschaftsverlag, München, Germany

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