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Synthesis and crystal structure of catena-poly[cobalt(II)-di-μ-chlorido-μ-pyridazine-κ(2) N (1):N (2)]
The reaction of cobalt dichloride hexahydrate with pyridazine leads to the formation of crystals of the title compound, [CoCl(2)(C(4)H(4)N(2))]( n ). This compound is isotypic to a number of compounds with other divalent metal ions. Its asymmetric unit consists of a Co(2+) atom (site symmetry 2/m),...
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/PMC10561210/ https://www.ncbi.nlm.nih.gov/pubmed/37817962 http://dx.doi.org/10.1107/S2056989023007065 |
Sumario: | The reaction of cobalt dichloride hexahydrate with pyridazine leads to the formation of crystals of the title compound, [CoCl(2)(C(4)H(4)N(2))]( n ). This compound is isotypic to a number of compounds with other divalent metal ions. Its asymmetric unit consists of a Co(2+) atom (site symmetry 2/m), a chloride ion (site symmetry m) and a pyridazine molecule (all atoms with site symmetry m). The Co(2+) cations are coordinated by four chloride anions and two pyridazine ligands, generating trans-CoN(4)Cl(2) octahedra, and are linked into [010] chains by pairs of μ-1,1-bridging chloride anions and bridging pyridazine ligands. In the crystal structure, the pyridazine ligands of neighboring chains are stacked onto each other, indicating π–π interactions. Powder X-ray diffraction proves that a pure crystalline phase was obtained. Differential thermonalysis coupled to thermogravimetry (DTA–TG) reveal that decomposition is observed at about 710 K. Magnetic measurements indicate low-temperature metamagnetic behavior as already observed in a related compound. |
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