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Synthesis and Structures of Vanadium(III) and Vanadium(IV) Silanolates The syntheses of the new and partially known vanadium(III)-silanolate complexes [{V(OSiMet2Bu)3}2(THF)] ( 1 ), [Li(THF)2V(OSiMet2Bu)4] ( 2 ), [V(OSiMet2Bu)(lut)] ( 3 ), V(OSiPh3)3(THF)3 ( 4 ), [Li(THF)4][V(OSiPh3)4](THF)2 ( 5 ), [Li(DME)VMes(OSiMet2Bu)3] ( 7 ), [Li(THF)4][VMes · (OSiPh3)3] ( 8 ), [Li(THF)4][VMes3(OSiMet2Bu)] ( 9 ), and Na[VMes3(OSiPh3)](THF)4 ( 10 ) as well as the vanadium(IV) compounds [V(OSiPh3)4] ( 6 ), [VMes3(OSiMet2Bu)] ( 11 ) and [VMes3(OSiPh3)] ( 12 ) are reported. In most cases the vanadium atom displays a coordination number of four. The dimeric structure of 1 with coordination numbers of four and five, respectively, has been deduced from molecular mass measurements, mass spectrometry and its magnetic properties. The crystal structures of compounds 2 , 4 , 5 , 9 and 11 were resolved. Complex 2 resembles a bridged contact ion pair in which both metal centres are in a tetrahedral coordination environment. In 4 the ligands are arranged trigonal bipyramidally with the THF molecules in the axial positions. Complexes 5 and 9 crystallize in separated ion paires with the vanadium in a tetrahedral coordination sphere. The crystal structure of 11 is analogous to that of 9 but with consequences due to the higher oxidation state. Oxidation of the vanadates(III), e. g. 5 , 9 and 10 , yields the corresponding vanadium(IV) compounds 6 , 11 and 12 . 相似文献
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I. V. Markova 《Journal of Analytical Chemistry》2002,57(9):821-825
It was shown that vanadium(V) and vanadium(IV) can be determined at a large Pt electrode in H2SO4 solutions in the presence of copper and bismuth by controlled-potential coulometry with RSD no worse than 0.2%. Compounds of the composition Bi4V1.8Cu0.2O10.7 – x
were analyzed. 相似文献
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Voltammetric and Spectroscopic Investigation of Complexation of Vanadium(IV) and Vanadium(V) by Carbonate Solutions which contain in addition to vanadium(IV) or vanadium(V), respectively, a high excess of bicarbonate or carbonate were studied by voltammetric and spectroscopic methods. A reversible electrode reaction occurs in the pH range 7–8 in 1 M KHCO3. While generating VIV from VV electrochemically a carbonate ligand is added to VIV. Based on ESR parameter recorded at room temperature and 77 K the existence of a VIV carbonato complex is suggested. A comparison of these ESR parameter with those of analogous VIV complexes leads to conclusions in view of the structure of the VIV carbonato complex. These structural suggestions are supported by the fact that VIV and VV form a mixed valent dimer in HCO3?/CO2-buffer of pH 7.5. Such dimers can be formed only when one of the oxygens of the VVO2+ cis-dioxo unit is able to coordinate at a basal site in the VIV-complex. Thus, conclusions regarding the arrangement of the carbonato ligands in the monomeric VV complex are possible too. A comparison of the complexes which are formed by VIV and VV with carbonate and the adducts arising from the interaction of VIV and VV with transferrin reveals the similarities of the both redox couples. 相似文献
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Determination of Vanadium(IV) and Vanadium(V) in Benfield Samples by IEC with Conductivity Detection
In this study, the determination of vanadium valence state, V(IV) and V(V) has been achieved using ion-exchange chromatography with conductivity detector. In this method, V(IV) was determined as V(IV)-EDTA complex and V(V) as vanadate ion. Determination of V(IV) was successfully done using 3 mM carbonate/bicarbonate/EDTA at pH 8.6 as the eluent. The additive, EDTA in the mobile phase did not seem to interfere with the V(IV) analysis. The detection of V(V) was achieved with 5 mM disodium hydrogen phosphate buffer at pH 10.4. A linear calibration graph over VO3 ? and V(IV) with concentration ranges 5–15 mg L?1 gave the detection limit at 0.09 and 0.1 mg L?1, respectively. Both V(IV) and V(V) were successfully determined in Benfield sample, with concentrations of V(IV) and V(V) at 4 and 11,000 mg L?1, respectively. 相似文献
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The new vanadium(II) complexes [V(opd)4]X2 and [V(mopd)4]X2, where opd = o-phenylenediamine, mopd = 4-methyl-o-phenylenediamine, and X = Cl or Br, have been prepared by reaction of the aromatic diamine with the vanadium(II) halide in EtOH. Magnetic measurements suggest that these contain octahedral vanadium(II) complex cations, and this is confirmed by the diffuse reflectance spectra. I.r. spectra suggest that the [V(opd)4]2+ cations contain two bidentate and two monodentate diamine ligands. 相似文献
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Hexacoordinate complexes of vanadium(III) containing tridentate ONS chelating substituted salicylaldehyde thiosemicarbazones have been prepared and characterised by elemental analysis, i.r. and u.v.–vis. spectroscopy and cyclic voltammetry. 相似文献
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The pink complexes of vanadium (V) and N-pyridylaminothioformyl-N′-phenylhydroxylamine are extractable into chloroform. Spectrophotometric studies show that the 1:2 complex predominates in the acidity range of 2.5-6 N HCl. The values of the stability constants, stepwise and overall, have been calculated following extended Yatsimirskii, Leden and Harvey-Manning methods. 相似文献
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Visible light facilitates a solid-to-solid photochemical aerobic oxidation of a hunter-green microcrystalline oxidovanadium(IV) compound (1) to form a black powder of cis-dioxidovanadium(V) (2) at ambient temperature. The siderophore ligand pyridine-2,6-bis(thiocarboxylic acid), H(2)L, is secreted by a microorganism from the Pseudomonas genus. This irreversible transformation of a metal monooxo to a metal dioxo complex in the solid state in the absence of solvent is unprecedented. It serves as a proof-of-concept reaction for green chemistry occurring in solid matrixes. 相似文献
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Kirillov A. I. Panezhda E. V. Vlasova N. N. Pozhidaev Yu. N. Minchenko O. A. Belousova L. I. Voronkov M. G. 《Russian Journal of Applied Chemistry》2001,74(6):950-953
Features of vanadium(V) sorption by cross-linked organosilicon polymers-polyorganylsilsesquioxanes containing acetamide, phthalamide, malondiamide, and thiourea dioxide functional substituents, were studied. 相似文献
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Annemarie Hollstein 《Fresenius' Journal of Analytical Chemistry》1964,202(4):288
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H. Zimmer und D. Klockow 《Fresenius' Journal of Analytical Chemistry》1965,211(5):366-367
Ohne Zusammenfassung 相似文献