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Search query: oxalato
321 articles match your search "oxalato"Results 1 to 10, sorted by relevance:
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Rb2Co(C2O4)2·4H2O consists of isolated [Co(C2O4)2·2H2O] octahedra which are connected only by hydrogen bonding of the water molecules. Rb2CoCl2(C2O4) consists of chains of Co2+ cations connected via oxalate bridging ligands. In K2Li2Cu(C2O4)3·2H2O, the metal cations are interconnected by oxalate ligands forming a novel three-periodic network.
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The polymorphism of Na[Rh(H2O)2(C2O4)2]·2H2O is noteworthy. The complex crystallizes with the formation of two different structures of the same water content. Oxalato-rhodic acid not only exists in solution, but, unlike most complex acids, it can also crystallize as a tetrahydrate.
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The structure of the title compound is made up of corrugated anionic layers of formula [BaCr(C2O4)3(H2O)3]nn– that leave voids accommodating the charge-compensating cations, [Ni(H2O)6]2+ (point group symmetry
), as well as the water molecules of crystallization.
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The single-crystal X-ray structure of [(18-crown-6)K][SnPh3(ox)] (ox = C2O42−) is reported. Integrity between neighboring molecules in the solid state is maintained by an array of C—H
O hydrogen bonds and C—H
π interactions.
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A novel coordination polymer is reported consisting of oxalate ligands bridging NaI and FeIII octahedra in an unusual μ2-coordination mode and forming infinite and zigzag chains linked via hydrogen bonds in a one-dimensional topology.
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The title compounds are two closely related oxalate-bridged dinuclear copper complexes. The histamine ligand is in a gauche conformation and coordinates to copper ions in a bidentate chelating fashion. The dinuclear complexes are linked to form three-dimensional networks via different types of hydrogen-bond and weak interactions.
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The phenomenon of spontaneous resolution of enantiomers occurs during the crystallization of the sodium and rubidium double salts of the transition metal complex tris(oxalato)ferrate(III).
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The structures of two new coordination polymers, ACr(C2O4)2(H2O)4, with A = Li (C2/m) and Na (P
), consist of alkali metal and Cr octahedra μ2-bridged by oxalate ligands. The resulting one-dimensional chains are connected together through hydrogen-bond motifs, leading to two-dimensional frameworks. However, they differ in the crystal packing, the hydrogen-bond networks and the oxygen disorder in the former polymer.
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[Co(en)3][Co(ox)3]·5H2O shows stereoselective hydrogen-bonding interactions depending on the axis of interaction of [Co(en)3]3+. This has implications for chiral discriminations in solution.
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The synthesis of complex compounds based on vanadium oxalates has grown considerably during the last decades, because of there biological and catalytic applications. This paper describes the synthesis and characterization of a new dioxovanadate(V) complex, (C5H8N3)3[VO2(C2O4)2]·2.5H2O.