Mukherjee Riya, Dougan Brenda A, Fry Fiona H, Bunge Scott D, Ziegler Christopher J, Brasch Nicola E
Department of Chemistry, Kent State University, Kent, Ohio 44242, School of Biosciences, University of Exeter, Exeter EX4 4QD, UK.
Inorg Chem. 2007 Mar 5;46(5):1575-85. doi: 10.1021/ic0613210. Epub 2007 Feb 6.
The formation of vanadium(III) complexes with nuclearity greater than two is believed to occur in aqueous solution on the basis of potentiometric, electrochemical, and/or UV-vis spectroscopy titration measurements, although structural evidence for this is limited. Upon the addition of 1-2 equiv of acetate, propionate, chloroacetate, trifluoroacetate, or bromoacetate to an aqueous, acidic solution of vanadium(III), trinuclear and tetranuclear complexes are formed. The structures of [V4(mu-OH)4(mu-OOCCF3)4(OH2)8]Cl4.7.5H2O (1), [V4(mu-OH)4(mu-OOCCH3)4(OH2)8]Cl4.CH3COOH.12H2O (2), [V4(mu-OH)4(mu-OOCCH3)4(OH2)8]Cl4.3H2O (3), [V3(mu3-O)(mu-OOCCH2Br)6(OH2)3]CF3SO3.H2O (4), [V3(mu3-O)(mu-OOCCH2CH3)6(OH2)3]Cl.2H2O (5), [V3(mu3-O)(mu-OOCCH3)6(OH2)3]Cl.3.5H2O (6), and [V3(mu3-O)(mu-OOCCH2Cl)6(OH2)3]CF3SO3.H2O (7) have been determined by X-ray diffraction. Importantly, electrospray mass spectrometry and 1H NMR measurements suggest that these complexes are not purely solid-state phenomena but are also present in solution. For the vanadium(III)/acetate and vanadium(III)/propionate systems, two paramagnetic 1H NMR signals corresponding to two distinct complexes (species A and B) are observed in the 40-55 ppm region for 0.20 mol equiv of acetate or propionate, at pD 3.44. No corresponding signals are observed for the vanadium(III)/bromoacetate and vanadium(III)/chloroacetate systems under the same conditions or for the vanadium(III)/ trifluoroacetate system using 19F NMR spectroscopy. UV-vis spectra suggest that species B are structurally analogous for the vanadium(III)/acetate and vanadium(III)/propionate systems, whereas structurally different complexes are the major species for the other systems. Diffusion coefficients of species B for the vanadium(III)/acetate and vanadium(III)/propionate systems determined by pulsed-field-gradient spin-echo NMR spectroscopy measurements are (3.0 +/- 0.1) x 10-6 and (3.23 +/- 0.01) x 10-6 cm2 s-1, respectively, and are most consistent with species B being trimeric, rather than tetranuclear, complexes.
基于电位滴定、电化学和/或紫外可见光谱滴定测量结果,人们认为在水溶液中会形成核数大于二的钒(III)配合物,不过这方面的结构证据有限。向钒(III)的酸性水溶液中加入1 - 2当量的乙酸盐、丙酸盐、氯乙酸盐、三氟乙酸盐或溴乙酸盐后,会形成三核和四核配合物。通过X射线衍射确定了[V4(μ-OH)4(μ-OOCCF3)4(OH2)8]Cl4·7.5H2O(1)、[V4(μ-OH)4(μ-OOCCH3)4(OH2)8]Cl4·CH3COOH·12H2O(2)、[V4(μ-OH)4(μ-OOCCH3)4(OH2)8]Cl4·3H2O(3)、[V3(μ3-O)(μ-OOCCH2Br)6(OH2)3]CF3SO3·H2O(4)、[V3(μ3-O)(μ-OOCCH2CH3)6(OH2)3]Cl·2H2O(5)、[V3(μ3-O)(μ-OOCCH3)6(OH2)3]Cl·3.5H2O(6)和[V3(μ3-O)(μ-OOCCH2Cl)6(OH2)3]CF3SO3·H2O(7)的结构。重要的是,电喷雾质谱和1H NMR测量表明,这些配合物并非纯粹的固态现象,在溶液中也存在。对于钒(III)/乙酸盐和钒(III)/丙酸盐体系,在pD 3.44条件下,当加入0.20摩尔当量的乙酸盐或丙酸盐时,在40 - 55 ppm区域观察到对应于两种不同配合物(A种和B种)的两个顺磁1H NMR信号。在相同条件下,钒(III)/溴乙酸盐和钒(III)/氯乙酸盐体系未观察到相应信号,使用19F NMR光谱对钒(III)/三氟乙酸盐体系也未观察到相应信号。紫外可见光谱表明,对于钒(III)/乙酸盐和钒(III)/丙酸盐体系,B种在结构上类似,而对于其他体系,结构不同的配合物是主要物种。通过脉冲场梯度自旋回波NMR光谱测量确定的钒(III)/乙酸盐和钒(III)/丙酸盐体系中B种的扩散系数分别为(3.0 ± 0.1)×10-6和(3.23 ± 0.01)×10-6 cm2 s-1,这与B种为三聚体而非四核配合物最为一致。