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Vanadium complexes ascorbic acid

Shriadah et al. [516] determined molybdenum VI in seawater by densitometry after enrichment as the Tiron complex on a thin layer of anion exchange resin. There were no interferences from trace elements or major constituents of seawater, except for chromium and vanadium. These were reduced by the addition of ascorbic acid. The concentration of dissolved molybdenum (VI) determined in Japanese seawater was 11.5 pg/1, with a relative standard deviation of 1.1%. [Pg.206]

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. [Pg.269]

C,Hk, 1,3-Cyclopentadiene, 1-methyl-, preparation and purification of, 27 52 titanium complex, 27 52 vanadium complex, 27 54, 55 QH,Oj, Ascorbic acid, platinum complex, 27 283... [Pg.378]

The chief interference is from Fe(lll), which forms a green complex with chromotropic acid. Before the determination of Ti, larger quantities of iron should be separated or smaller ones reduced with ascorbic acid or sulphite. Vanadium in quantities not exceeding those of titanium has no appreciable effect on the determination of Ti. Molybdenum at concentrations below 50 pg/ml does not interfere. Fluoride interferes by masking titanium, but can be removed by fuming with H2SO4. Oxidants (e.g. HNO3) must be absent because chromotropic acid is fairly easily oxidized. [Pg.440]

Protonated carboxylic acid complexes of vanadium(v) have been identified as catalysts in the oxidation of aniline by chlorate. The oxidation of ascorbic acid... [Pg.53]

The first term is the law observed in the absence of catalyst. The effect is dramatic, however, with associated rate constants ko and ki being 50.3 1 mol s and 3.43 x 10 1 mol s respectively, and may be ascribed to the formation of a Mo -BrOa" complex with no evidence for any change in the oxidation state of the catalyst during the course of the reaction. The kinetics and mechanism of the bromate-ascorbic acid reaction have also been reported, and the effects of phosphate on the oxidation of iodide by chlorate in the presence of catalytic concentrations of vanadium(iv) have been described, the latter systems being considered to involve vanadium(iv)-phosphate complexes. [Pg.76]


See other pages where Vanadium complexes ascorbic acid is mentioned: [Pg.1169]    [Pg.1438]    [Pg.493]    [Pg.351]    [Pg.4]    [Pg.155]    [Pg.173]    [Pg.149]    [Pg.203]    [Pg.475]    [Pg.188]    [Pg.350]    [Pg.442]    [Pg.12]    [Pg.519]    [Pg.86]   
See also in sourсe #XX -- [ Pg.3 , Pg.502 ]




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Vanadium complexes

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