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Bis(methanol-1κO)tetra-μ-pyridazine-1:2κ(4) N:N′;2:3κ(4) N:N′-di-μ-thio­cyanato-1:2κ(2) N:N;2:3κ(2) N:N-tetrathio­cyanato-1κ(2) N,3κ(2) N-trinickel(II) methanol tetra­solvate

Reaction of an excess nickel(II) thio­cyanate with pyridazine leads to single crystals of the title compound, [Ni(3)(NCS)(6)(N(2)C(4)H(4))(4)(CH(3)OH)(2)]·4CH(3)OH. The crystal structure consists of trimeric discrete complexes, in which two Ni(II) cations are coordinated by two terminal and one μ-1,...

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Detalles Bibliográficos
Autores principales: Wöhlert, Susanne, Jess, Inke, Näther, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3393200/
https://www.ncbi.nlm.nih.gov/pubmed/22807768
http://dx.doi.org/10.1107/S1600536812026864
Descripción
Sumario:Reaction of an excess nickel(II) thio­cyanate with pyridazine leads to single crystals of the title compound, [Ni(3)(NCS)(6)(N(2)C(4)H(4))(4)(CH(3)OH)(2)]·4CH(3)OH. The crystal structure consists of trimeric discrete complexes, in which two Ni(II) cations are coordinated by two terminal and one μ-1,1 bridging thio­cyanato anions, one methanol mol­ecule and two bridging pyridazine ligands, whereas the central Ni(II) atom is coordinated by two μ-1,1 bridging anions as well as four bridging pyridazine ligands. The asymmetric unit consists of two crystallographically independent Ni cations, one of which is located on a center of inversion, as well as three crystallographically independent thio­cyanato anions, two pyridazine ligands and three independent methanol mol­ecules in general positions. Two of the solvent mol­ecules do not coordinate to the metal atoms and are located in cavities of the structure. The discrete complexes are linked by inter­molecular O—H⋯O and O—H⋯S hydrogen bonding into layers parallel to the bc plane.