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首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >Syntheses and spectroscopic and structural characterization of molybdenum(VI) citrato monomeric raceme and dimer, K-4[MoO3(cit)]center dot 2H(2)O and K-4[(MoO2)(2)O(Hcit)(2)]center dot 4H(2)O
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Syntheses and spectroscopic and structural characterization of molybdenum(VI) citrato monomeric raceme and dimer, K-4[MoO3(cit)]center dot 2H(2)O and K-4[(MoO2)(2)O(Hcit)(2)]center dot 4H(2)O

机译:柠檬酸钼(VI)单体外消旋体和二聚体,K-4 [MoO3(cit)]中心点2H(2)O和K-4 [(MoO2)(2)O(Hcit)(2)的合成,光谱和结构表征)]中心点4H(2)O

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Investigation of the aqueous coordination chemistry for citrate and molybdenum(VI) resulted in the isolation of molybdenum(VI) citrate monomeric raceme and dimer K-4[MoO3(cit)] . 2H(2)O (1) and K-4[(MoO2)(2)O(HCit)(2)] . 4H(2)O (2) (H(4)cit = citric acid). Complex 1 can serve as the first structurally characterized monomeric citrate molybdate and may represent an early mobilized precursor in the biosynthesis of FeMo-co (FeMo-cofactor). The two complexes have been characterized by elemental analyses and IR and NMR spectroscopies. The IR and NMR spectra are consistent with a monomeric species or a monooxo-bridged dinuclear structure, as revealed by a single crystal X-ray diffraction study. Compound 1 is monoclinic space group P2(1)/c with a = 7.225(1) Angstrom, b = 9.151(2) Angstrom, c = 22.727(2) Angstrom, beta = 94.93(1)degrees,V = 1497.1(7) Angstrom(3), and Z = 4. Full-matrix least,squares refinement resulted in residuals of R = 0.027 and R-w = 0.032. The molybdenum atom forms an octahedral coordination with three oxo groups and one tridentate citrate, in which the latter is coordinated through the alkoxy and vicinal carboxyl and much more weakly by one of the two terminal groups [2.411(3) Angstrom]. Compound 2 is triclinic space group P1 with 8.2728(8) Angstrom. b = 8.9514(8) Angstrom, c = 10.0605(9) Angstrom, alpha = 101.673(8)degrees, beta = 100.672(7)degrees, gamma = 112.938(7)degrees, V = 642.5(3) Angstrom(3), and Z = 1. Full-matrix least-squares refinement resulted in residuals of R = 0.033 and R-w = 0.039. The complex anion contains a linear (O2Mo)O(MoO2) core with the bridging oxo group lying at the center of inversion symmetry (Mo-O-b-Mo, 180 degrees). Each citrate ligand is three-coordinated to one molybdenum atom through the deprotonated hydroxy, alpha-carboxyl, and one beta-carboxyl group, making each metal atom six-coordinate. [References: 49]
机译:对柠檬酸和钼(VI)的水配位化学的研究导致柠檬酸钼(VI)单体外消旋体和二聚体K-4 [MoO3(cit)]的分离。 2H(2)O(1)和K-4 [(MoO2)(2)O(HCit)(2)]。 4H(2)O(2)(H(4)cit =柠檬酸)。配合物1可以作为第一个在结构上表征的单体柠檬酸钼酸盐,并且可以代表FeMo-co(FeMo-辅因子)生物合成中的早期动员前体。两种配合物已通过元素分析,IR和NMR光谱表征。单晶X射线衍射研究表明,IR和NMR光谱与单体种类或单氧桥双核结构一致。化合物1是单斜空间群P2(1)/ c,其a = 7.225(1)埃,b = 9.151(2)埃,c = 22.727(2)埃,beta = 94.93(1)度,V = 1497.1(7) )Angstrom(3),Z =4。最小全矩阵,平方细化导致R = 0.027和Rw = 0.032的残差。钼原子与三个氧代基团和一个柠檬酸三齿基团形成八面体配位,其中后者通过烷氧基和邻位羧基配位,而通过两个末端基团之一更弱地配位[2.411(3)埃]。化合物2是具有8.2728(8)埃的三斜空间群P1。 b = 8.9514(8)埃,c = 10.0605(9)埃,alpha = 101.673(8)度,beta = 100.672(7)度,γ= 112.938(7)度,V = 642.5(3)埃(3) ,并且Z =1。全矩阵最小二乘优化导致残差R = 0.033和Rw = 0.039。复合阴离子包含一个线性(O2Mo)O(MoO2)核,其桥联氧代基位于反对称对称中心(Mo-O-b-Mo,180度)。每个柠檬酸盐配体通过去质子化的羟基,α-羧基和一个β-羧基与一个钼原子三配位,从而使每个金属原子六配位。 [参考:49]

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