Abstract
In the title compound, [CuCl(C10H8N2)2]2[Bi2Cl4(C7H3NO4)2(H2O)2]·5H2O, the dianion [Bi2Cl4(C7H3NO4)2(H2O)2]2− is located about an inversion center. The CuII atom of the cation is coordinated by four N atoms of the two chelating 2,2′-bypyridine ligands and one Cl− ion, completing a distorted trigonal–bipyramidal coordination environment. In the anion, each BiIII atom is seven-coordinate and is bonded to a tridentate pyridine-2,6-dicarboxylate ligand, a water molecule, two chloride ions and a bridging carboxylate O atom of another carboxylate ligand. The coordination geometry of BiIII is distorted pentagonal–bipyramidal with the Cl− ions located in axial positions. The structure of the dianion is additionally stabilized by an intramolecular O—H⋯O hydrogen bond between the coordinated water molecule and carboxylate O atom. In the crystal, O—H⋯O hydrogen bonds occur . The H atoms of the solvent water molecules could not be located.
Highlights
In the title compound, [CuCl(C10H8N2)2]2[Bi2Cl4(C7H3NO4)2(H2O)2]5H2O, the dianion [Bi2Cl4(C7H3NO4)2(H2O)2]2 is located about an inversion center
The CuII atom of the cation is coordinated by four N atoms of the two chelating 2,20 bypyridine ligands and one Cl ion, completing a distorted trigonal–bipyramidal coordination environment
BiIII is distorted pentagonal–bipyramidal with the Cl ions located in axial positions
Summary
College of Chemistry and Pharmacy Engineering, Nanyang Normal University, Nanyang 473061, People’s Republic of China, and bDepartment of Equipment and
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