metal-organic compounds
The title compound, [Cu(C9H5N2O3)2(C2H6OS)2], consists of octahedrally coordinated CuII ions, with the 3-oxo-3,4-dihydroquinoxaline-2-carboxylate ligands acting in a bidentate manner [Cu—O = 1.9116 (14) Å and Cu—N = 2.1191 (16) Å] and a dimethyl sulfoxide (DMSO) molecule coordinated axially via the O atom [Cu—O = 2.336 (5) and 2.418 (7) Å for the major and minor disorder components, respectively]. The whole DMSO molecule exhibits positional disorder [0.62 (1):0.38 (1)]. The octahedron around the CuII atom, which lies on an inversion centre, is elongated in the axial direction, exhibiting a Jahn–Teller effect. The ligand exhibits tautomerization by H-atom transfer from the hydroxyl group at position 3 to the N atom at position 4 of the quinoxaline ring of the ligand. The complex molecules are linked through an intermolecular N—HO hydrogen bond [NO = 2.838 (2) Å] formed between the quinoxaline NH group and a carboxylate O atom, and by a weak intermolecular C—HO hydrogen bond [3.392 (11) Å] formed between a carboxylate O atom and a methyl C atom of the DMSO ligand. There is a weak intramolecular C—HO hydrogen bond [3.065 (3) Å] formed between a benzene CH group and a carboxylate O atom.
metal-organic compounds
In the title compound, [Cd(C7H6NO2)2]n, the CdII ion has a distorted octahedral geometry. The 6-methylpyridine-2-carboxylate anions are perpendicular to one another and act as bidentate and bridging ligands. Two carboxylate O atoms bridge the CdII ions, forming centrosymmetric dinuclear units. These units are further connected via carboxylate O atoms into a one-dimensional polymeric chain which extends in the [100] direction.
metal-organic compounds
In the title compound, [Ni(N3)2(C6H6N2O)2], the NiII atom lies on an inversion centre. The distorted octahedral nickel(II) coordination environment contains two planar trans-related N,O-chelating picolinamide ligands in one plane and two monodentate azide ligands perpendicular to this plane. Molecules are linked into a three-dimensional framework by N—HN hydrogen bonds.
metal-organic compounds
In the title compound, [Hg(NO3)(C6H6N2O)2]NO3, the HgII atom is five-coordinate. The distorted square-pyramidal mercury(II) coordination environment is achieved by two N,O-bidentate picolinamide ligands, with one O-monodentate nitrate ion in the apical position. A seven-coordinate extended coordination environment is completed by two additional weak HgO interactions, one from the coordinated nitrate ion and one from the other nitrate ion, to give seven-coordination. The molecules are linked into a two-dimensional network by N—HO hydrogen bonds.
metal-organic compounds
The title compound, [Co(C7H6NO2)2(H2O)4]·4H2O, contains a CoII ion lying on a crystallographic inversion centre. The CoII ion is octahedrally coordinated by two 6-methylpyridine-3-carboxylate ligands in axial positions [Co—O = 2.0621 (9) Å] and by four water molecules in the equatorial plane [Co—O = 2.1169 (9) and 2.1223 (11) Å]. There are also four uncoordinated water molecules. The 6-methylpyridine-3-carboxylate ligands are bound to the CoII ion in a monodentate manner through a carboxylate O atom. There is one strong intramolecular O—HO hydrogen bond, and six strong intermolecular hydrogen bonds of type O—HO and one of type O—HN in the packing, resulting in a complex three-dimensional supramolecular structure.