metal-organic compounds
Open access
The title mononuclear CuII complex, [Cu(C9H7O2)2(C12H8N2)], is comprised of a CuII cation, two cinnamate (L−) ligands and a 1,10-phenanthroline (phen) ligand. The CuII atom and phen ligand lie on a twofold rotation axis. The CuII atom is coordinated by two O atoms from two carboxylate groups of two (L−) ligands and two N atoms from one phen ligand, exhibiting a distorted square-planar geometry. In the crystal, molecules are assembled into supramolecular chains parallel to the c axis through weak C—HO hydrogen bonds involving the phen and cinnamate ligands.
metal-organic compounds
Open access
The title polymeric compound, [Cu2(C8H7O2)4]n, was synthesized by the reaction of copper acetate with aqueous phenylacetic acid. The unique CuII atom is coordinated by five O atoms from the carboxylate groups of phenylacetate ligands, and the strongly distorted octahedral coordination environment is completed by a Cu—Cu bond of 2.581 (2) Å, at whose mid-point is located an inversion centre. The crystal structure consists of infinite polymeric linear chains of Cu2+ ions, running along [100], linked by bridging phenylacetate groups.
metal-organic compounds
Open access
The title compound, [Co2(C8H7O2)4(C7H10N2)2], crystallizes as a centrosymmetric dimer containing two CoII atoms bridged by four bidentate phenylacetate ligands in syn–syn bridging modes. Each CoII atom is five-coordinated by four O atoms from four different carboxylate ligands and the ring N atom of a 4-(dimethylamino)pyridine unit, generating a distorted square-pyramidal geometry in which the four O atoms form the basal plane and the N atom occupies the axial position. In the crystal, C—HO interactions link the dinuclear complex molecules into a three-dimensional network.