The binuclear title complex, [Co(2)(C(18)H(26)N(4)O(12))(H(2)O)(2)]·4H(2)O, lies about a centre of inversion, the Co(II) atom being coordinated in a distorted octa-hedral arrangement defined by one water mol-ecule and N(2)O(3) donors derived from one end of a 6,9-bis(carboxylatomethyl)-3,12-bis(car-boxy-methyl)-3,6,9,12-tetraaza-tetradecanedioate (H(2)TTHA(4-)) tetra-anion. In the crystal, numerous O-H⋯O hydrogen bonds link the mol-ecules into a three-dimensional network.
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http://dx.doi.org/10.1107/S1600536813000196 | DOI Listing |
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September 2021
Laboratoire de Chimie Minérale et Analytique (LACHIMIA), Département de Chimie, Faculté des Sciences et Techniques, Université Cheikh Anta Diop, Dakar, Senegal.
The title compound, (NH)[W(CHNO)O]·4HO, was obtained from a mixture of tungstic acid, ammonia and ethyl-enedi-amine-tetra-acetic acid (Hedta) in a 2:4:1 ratio. The anion of the complex contains two WO units and one bridging edta ligand. Each central metal atom is tridentately coordinated by nitro-gen and two carboxyl-ate groups of the edta ligand, together with the three oxido ligands, producing a distorted octa-hedral coordination environment around each tungsten atom.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
December 2018
National University of Life and Environmental Science of Ukraine, Kyiv, Ukraine.
The title compound, [Pd(CHN)(CHOP)]·4HO, comprises of a binuclear mol-ecule (point group symmetry 2), with a twofold rotation axis running through the central C atom of the methyl-enedi-phospho-nate (MDP) anion. The Pd atom has a square-planar coordination environment defined by the N atoms of a bidentate ethyl-enedi-amine (en) ligand and two O atoms of the bridging MDP anion. In the crystal structure, metal complexes are arranged in layers parallel (001) and are sandwiched between layers containing disordered water mol-ecules of crystallization.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
October 2016
Institute of Physics, University of Neuchâtel, rue Emile-Argand 11, CH-2000 Neuchâtel, Switzerland.
The title isotypic complexes, bis-[μ-5,6-bis-(pyridin-2-yl)pyrazine-2,3-di-carboxylato]-κ,,:;κ:,,-bis-[di-aqua-manganese(II)] tetra-hydrate, [Mn(CHNO)(HO)]·4HO, (I), and bis-[μ-5,6-bis-(pyridin-2-yl)pyrazine-2,3-di-carboxyl-ato]-κ,,:;κ:,,-bis-[di-aqua-iron(II)] tetrahydrate, [Fe(CHNO)(HO)]·4HO, (II), are, respectively, the mangan-ese(II) and iron(II) complexes of the ligand 5,6-bis-(pyridin-2-yl)-pyrazine-2,3-di-carb-oxy-lic acid. The complete mol-ecule of each complex is generated by inversion symmetry. Each metal ion is coordinated by a pyrazine N atom, a pyridine N atom, two carboxyl-ate O atoms, one of which is bridging, and two water O atoms.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
April 2016
Department of Chemistry, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla 90112, Thailand.
In the title compound, [Ag2(C3H6N2S)4(C18H15P)2](C2H3O2)2·[Ag(C2H3O2)(C3H6N2S)(C18H15P)2]2·2C2H3N·4H2O, the Ag(I) ion in the mononuclear neutral complex exhibits a distorted tetra-hedral environment with coordination by two P atoms from tri-phenyl-phosphane (PPh3) ligands, one S atom of an imidazolidine-2-thione (etu) ligand and one O atom of an acetate anion. The binuclear cationic complex comprises two inversion-related [Ag(C3H6N2S)2(C18H15P)] units with Ag(I) ions bridged by two S atoms from etu ligands forming a four-membered Ag-S-Ag-S ring. Each Ag(I) ion is coordinated by a P atom of a PPh3 ligand, two S atoms of bridging etu ligands and the terminal S atom of an etu ligand in a distorted tetra-hedral environment.
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March 2015
Institute of Molecular Science, Key Laboratory of Chemical Biology and Molecular Engineering of the Education Ministry, Shanxi University, Taiyuan, Shanxi 030006, People's Republic of China.
The reaction of ZnO and tri-ethyl-ene-tetra-minehexaacetic acid (H6TTHA) in aqueous solution after refluxing yields the binuclear title compound, [Zn2(C18H26N4O12)(H2O)2]·4H2O. There is a centre of symmetry in the [Zn2(H2TTHA)(H2O)2] mol-ecule in the crystalline state. Both Zn(II) ions are octahedrally surrounded and bound by an N2O3 donor set from the H2TTHA(4-) anion and a water mol-ecule; the N atoms are cis and the water mol-ecule is trans to an N atom.
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