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Dichlorido[μ-10,21-dimethyl-2,7,13,18-tetraphenyl-3,6,14,17-tetraazatricyclo[17.3.1.1(8,12)]tetracosa-1(23),2,6,8,10,12(24),13,17,19,21-decaene-23,24-diolato]dicopper(II) ethanol hemisolvate dihydrate
The dinuclear title complex, [Cu(2)(C(46)H(38)N(4)O(2))Cl(2)]·0.5C(2)H(5)OH·2H(2)O, is located on crystallographic inversion centres with two half-molecules in the asymmetric unit. The two Cu(II) atoms are coordinated by a hexadentate dianionic ligand formed in situ from the condensation of two tr...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3011775/ https://www.ncbi.nlm.nih.gov/pubmed/21589231 http://dx.doi.org/10.1107/S1600536810042248 |
Sumario: | The dinuclear title complex, [Cu(2)(C(46)H(38)N(4)O(2))Cl(2)]·0.5C(2)H(5)OH·2H(2)O, is located on crystallographic inversion centres with two half-molecules in the asymmetric unit. The two Cu(II) atoms are coordinated by a hexadentate dianionic ligand formed in situ from the condensation of two tridentate ligands by four imine N atoms and two bridging phenolate O atoms along with two Cl atoms at axial positions. The coordination geometry around the metal atoms is distorted square-pyramidal (τ = 0.185 and 0.199). The non-bonding Cu⋯Cu distances are 2.9556 (12) and 2.9506 (12) Å in the two dimers. The packing is stabilized through solvent-mediated intermolecular O—H⋯O and O—H⋯Cl hydrogen bonds. The diamine chain of one of the dimers is disordered over two positions in a 0.680 (5):0.320 (5) ratio. |
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