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Synthesis, crystal structure and properties of bis(isoselenocyanato-κN)tetrakis(4-methoxypyridine-κN)cobalt(II)
Reaction of CoCl(2)·6H(2)O with KNCSe and 4-methoxypyridine in water led to the formation of the title compound, [Co(NCSe)(2)(C(6)H(7)NO)(4)] or Co(NCSe)(2)(4-methoxypyridine)(2), which was characterized by single-crystal X-ray diffraction. Its asymmetric unit consists of one crystallographicall...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9993910/ https://www.ncbi.nlm.nih.gov/pubmed/36909984 http://dx.doi.org/10.1107/S2056989023001391 |
Sumario: | Reaction of CoCl(2)·6H(2)O with KNCSe and 4-methoxypyridine in water led to the formation of the title compound, [Co(NCSe)(2)(C(6)H(7)NO)(4)] or Co(NCSe)(2)(4-methoxypyridine)(2), which was characterized by single-crystal X-ray diffraction. Its asymmetric unit consists of one crystallographically independent Co cation, two selenocyanate anions and four 4-methoxypyridine coligands in general positions. In the crystal structure, the cobalt cations are sixfold coordinated by two terminal N-bonded selenocyanate anions and four 4-methoxypyridine coligands within a slightly distorted octahedral coordination. Between the complexes, weak C—H⋯Se interactions are found. IR spectroscopic investigations revealed that the CN stretching vibration of the anionic ligands is observed at 2068 cm(−1), which is in agreement with the presence of only terminally coordinated selenocyanate anions. PXRD measurements prove that a pure compound was obtained. Differential thermoanalysis coupled to thermogravimetry (DTA-TG) at different heating rates shows that the TG curves are poorly resolved. PXRD measurements of the residue obtained by a TG measurement prove that an amorphous compound was obtained. |
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