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The cobalt(II) salt of the azo dye Orange G
Crystallizing the cobalt(II) salt of the azo dye Orange G from water was found to give the solvent-separated ion-pair species hexaaquacobalt(II) 7-oxo-8-(2-phenylhydrazin-1-ylidene)-7,8-dihydronaphthalene-1,3-disulfonate tetrahydrate, [Co(H(2)O)(6)](C(16)H(10)N(2)O(7)S(2))·4H(2)O. The asymmetri...
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/PMC2983163/ https://www.ncbi.nlm.nih.gov/pubmed/21587462 http://dx.doi.org/10.1107/S1600536810037360 |
Sumario: | Crystallizing the cobalt(II) salt of the azo dye Orange G from water was found to give the solvent-separated ion-pair species hexaaquacobalt(II) 7-oxo-8-(2-phenylhydrazin-1-ylidene)-7,8-dihydronaphthalene-1,3-disulfonate tetrahydrate, [Co(H(2)O)(6)](C(16)H(10)N(2)O(7)S(2))·4H(2)O. The asymmetric unit of the cobalt(II) salt contains three independent octahedral [Co(OH(2))(6)](2+) cations, three azo anions, all with similar configurations, and 12 uncoordinated water molecules. The structure is closely related to that of one of the known magnesium analogues. Both structures have Z′ = 3, feature nearly planar azo anions [maximum displacement of azo-N atoms from the plane of the phenyl ring = 0.058 (7) Å] in their hydrazone tautomeric form, form layer structures with hydrophilic and hydrophobic layers alternating along the b-axis direction, and are stabilized by an extensive network of hydrogen bonds.. |
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