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Synthesis, crystal structure and thermal properties of bis(1,3-dicyclohexylthiourea-κS)bis(isothiocyanato-κN)cobalt(II)
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-dicyclohexylthiourea in ethanol. Its crystal structure consists of discrete complexes that are located on twofold rotation axes, in which the Co(II) cations are tetrahedrally c...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8739206/ https://www.ncbi.nlm.nih.gov/pubmed/35079428 http://dx.doi.org/10.1107/S205698902101327X |
Sumario: | 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-dicyclohexylthiourea in ethanol. Its crystal structure consists of discrete complexes that are located on twofold rotation axes, in which the Co(II) cations are tetrahedrally coordinated by two terminal N-bonded thiocyanate anions and two 1,3-dicyclohexylthiourea ligands. These complexes are linked via intermolecular N—H⋯S and C—H⋯S hydrogen bonding into chains, which elongate in the b-axis direction. These chains are closely packed in a pseudo-hexagonal manner. The CN stretching vibration of the thiocyanate anions located at 2038 cm(−1) is in agreement with only terminal bonded anionic ligands linked to metal cations in a tetrahedral 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. |
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