Vanadium complexes reducing agents

The ability of metal ions to form complexes with formazans is utilized to determine these ions either directly (for low valent reducing ions) or indirectly in the presence of a reducing agent. Among others, molybdenum(VI) and vanadium(V) have been determined using this method.442,443 Indirect methods have been reported for the analyses of substances that do not reduce tetrazolium salts. Examples include arsenic in nickel ores436 and traces of selenium.437 A method for the extraction and analysis of a number of metal ternary ion association complexes has been described.444 - 448... 

It is not clear whether V(V) or V(IV) (or both) is the active insulin-mimetic redox state of vanadium. In the body, endogenous reducing agents such as glutathione and ascorbic acid may inhibit the oxidation of V(IV). The mechanism of action of insulin mimetics is unclear. Insulin receptors are membrane-spanning tyrosine-specific protein kinases activated by insulin on the extracellular side to catalyze intracellular protein tyrosine phosphorylation. Vanadates can act as phosphate analogs, and there is evidence for potent inhibition of phosphotyrosine phosphatases (526). Peroxovanadate complexes, for example, can induce autophosphorylation at tyrosine residues and inhibit the insulin-receptor-associated phosphotyrosine phosphatase, and these in turn activate insulin-receptor kinase. 

V(OH)2 is a strong reducing agent and freshly prepared V(OH)2 reacts with water with dihydrogen evolution. In acidic solution, reduction of water may be induced by UV radiation.138 From solutions containing complexes with catechol there is evolution of dihydrogen with simultaneous oxidation of the metal to vanadium(III). The reaction is first order in vanadium(II) and autocatalytic (Scheme 7).145... 

For the vanadophore region, the sulfate concentration has been estimated to be of the order of 1.3 M and pH 2.349 With no evidence for a stable complex within the vanadocyte, Figure 14 depicts an interesting mechanism proposed for vanadium and sulfate accumulation.350 Anionic vanadium(V) (as HVO ") and sulfate ions enter the cell. Provided that within the vanadophore there is a strong reducing agent, vanadium can be reduced to vanadium(IV) and vanadium(III), cationic at the low pH in the vanadophore. If the vanadophore membrane is permeable to anions but not cations, the reduced vanadium remains trapped. 

Cysteine is a fairly effective reducing agent for vanadate, but even so, under neutral conditions, the V(V) lifetime is sufficiently long that vanadium NMR spectra can be obtained. Four products (-243, -309, -393, and -405 ppm) have been reported. Of these complexes, the -243 and -309 ppm NMR signals apparently correspond to products containing two thiolate groups in the coordination sphere, whereas the -393 and -409 ppm products have one thiolate ligand [43],... 

Chemical Methods. In general, vanadium is reduced to the +II oxidation state by zinc amalgam, the vanadium can then be determined volumetrically by oxidation with a standard oxidizing agent (e.g. KMn04) to the +V state. The formation of the reddish-brown peroxo-complex is used as the basis of a colorimetric technique for the determination of vanadium. Gravimetric techniques are not as useM for the determination of vanadium as the volumetric and colorimetric techniques. 

The equilibrium constant of reaction (1), K = [Cu ][Cu ]/[Cu ], is of the order of 10 thus, only vanishingly small concentrations of aquo-copper(I) species can exist at equilibrium. However, in the absence of catalysts for the disproportionation—such as glass surfaces, mercury, red copper(I) oxide (7), or alkali (311)—equilibrium is only slowly attained. Metastable solutions of aquocopper(I) complexes may be generated by reducing copper(II) salts with europium(II) (113), chromium(II), vanadium(II) (113, 274), or tin(II) chloride in acid solution (264). The employment of chromium(II) as reducing agent is best (113), since in most other cases further reduction to copper metal is competitive with the initial reduction (274). 

Aquocopper(I) complexes are fairly powerful reducing agents and the kinetics of their reactions with iron(III) (275), vanadium(IV) (312), cobalt(III), and mercury(II) (113) have been studied. Further, the role of copper(I) species in the copper(II)-catalyzed reduction of cobalt(III) by vanadium(II) (112) has been confirmed with the reduction of... 

Catechols (and pyrogallols) readily reduce vanadium(V) to vanadium(IV) and, in some instances, further to vanadium(III). In the context of tunichromes as the presumed reducing agents in ascidians, the redox chemistry of catecholatovanadium complexes has been investigated to some extent. Results on reduction potentials for the and... 

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