Crystals of the title compound, [Co(NCS)(2)(C(13)H(24)N(2)S)(2)], were obtained by the reaction of Co(NCS)(2) with 1,3-di-cyclo-hexyl-thio-urea in ethanol. Its crystal structure consists of discrete complexes that are located on twofold rotation axes, in which the Co(II) cations are tetra-hedrally coordinated by two terminal N-bonded thio-cyanate anions and two 1,3-di-cyclo-hexyl-thio-urea ligands. These complexes are linked via inter-molecular N-Hâ¯S and C-Hâ¯S hydrogen bonding into chains, which elongate in the b-axis direction. These chains are closely packed in a pseudo-hexa-gonal manner. The CN stretching vibration of the thio-cyanate anions located at 2038â cm(-1) is in agreement with only terminal bonded anionic ligands linked to metal cations in a tetra-hedral coordination. TG-DTA measurements prove the decomposition of the compound at about 227°C. DSC measurements reveal a small endothermic signal before decomposition at about 174°C, which might correspond to melting.
Synthesis, crystal structure and thermal properties of bis-(1,3-di-cyclo-hexyl-thio-urea-κS)bis(iso-thiocyanato-κN)cobalt(II).
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作者:Krebs Christoph, Jess Inke, Näther Christian
| 期刊: | Acta Crystallographica Section E: Crystallographic Communications | 影响因子: | 0.500 |
| 时间: | 2022 | 起止号: | 2022 Jan 1; 78(Pt 1):71-75 |
| doi: | 10.1107/S205698902101327X | ||
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