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SynthesisandCrystalStructureof[Na(DB18C6)(CH_3OH)]_2Mo_6O_(19)·(DB18C6)·(CH_3OH)¥ZhouYin-Zhuang;TuShu-Jie;JinXiang-Lin;LiuShun-... 相似文献
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Synthesis and Structural Characterization of [(C_2H_5)_4N][V~((V))O_2(OC_6H_3(OCH_3)CHNNCSNH_2)]·H_2O 总被引:1,自引:1,他引:0
1 INTRODUCTIONAlthough vanadium plays an increasingly recognized role as a biometal[1~4], little is known about the structure and function of vanadium compounds in living organisms. A classical and nevertheless rapidly developing field of application for oxovanadates and related compounds is their use as catalysts in polymerization and oxidation reactions[5,6], and recent interest has focused on oxovanadates as model compounds for the interaction of oxovanadates with the active sites of en… 相似文献
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The reaction of VO(acac)2 with 2-hydroxyl-1-naphthaldehyde isonicotinyl hydrazone and amines (ethylenediamine or diethylenetriamine) in CH3OH yields crystals of novel vanadium compounds characterized by IR, NMR spectroscopic methods and X-ray single-crystal structure determination. Two different vanadium units exist in the crystal cell of [VO2(C17H11N3O2)][VO- (C4H13N3)(C6H5N3O)](C2H5OH) which crystallizes in the triclinic system, space group P1 with a = 8.0104(17), b = 13.898(3), c = 14.955(3)A, α = 89.103(4), β = 79.551(4), γ = 78.352(4)°, V = 1603.3(6)A^3, Mr = 723.54, Dc = 1.499 g/cm^3, Z = 2, λ(MoKα) = 0.71073 ]A,μ= 0.644 mm^-1, F(000) = 748, the final R = 0.0547 and wR = 0.0997 for 8920 observed reflections with I 〉 2σ(I). According to structure analysis, two different molecules are arranged in the lattice and the two vanadium atoms adopt octahedral and square pyramidal coordination geometries, respectively. The interactions between DNA and vanadium complexes have been investigated by UV-Vis absorption spectro- photometry. 相似文献
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The mononuclear copper(Ⅱ) complex [Cu(L)(2-AP)] 1 and binuclear copper(Ⅱ)complex [Cu(L)(py)]2 2 (L = C1oH1 1O5NS, taurine o-vanillin, py = prydine, 2-AP = 2-aminopyridine)with mixed ligand have been synthesized and characterized by X-ray diffraction method. Crystal data for 1: orthorhombic, space group Pbca with a = 11.921(4), b = 15.816(6), c = 17.076(6) (A), V=3219.7(19) (A)3, C15H17CuN3O5S, Z = 8, Mr = 414.92, Dc = 1.712 g/cm3,μ(MoKα) = 1.520 mm-1,F(000) = 1704, the final R = 0.0300 and wR = 0.0705 for 2840 observed reflections with I > 2σ(I);and crystal data for 2: monoclinic, space group P21/c with a = 7.929(3), b = 17.038(5), c = 11.734(4)(A), β = 98.162(6)°, V = 1569.1 (9) (A)3, C15H16CuN2O5S, Z = 4, Mr = 399.90, Dc = 1.693 g/cm3, F(000)= 820,μ(MoKα) = 1.554 mm-1, the final R = 0.0351 and wR = 0.0848 for 2767 observed reflections (I > 2o(I)). The molecular structure of complex 1 consists of one tetra-coordinated Cu(Ⅱ) atom generating a slightly distorted square plane, and a one-dimensional chain structure is formed by intermolecular hydrogen bonds. Complex 2 consists of a diphenolic hydroxyl O-bridged binuclear copper(Ⅱ) structure. The crystal structures of complexes 1 and 2 reveal that the coordinate copper centers are bound to both nitrogen and oxygen atom donors. The usual N,O-trans arrangement of ligands is observed in both cases. 相似文献