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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1489-1495 
    ISSN: 1434-1948
    Keywords: Peroxo complexes ; Vanadium ; Mass spectrometry ; 51V-NMR spectroscopy ; Vanadium dependent bromoperoxidases ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ESI mass spectrometry and 51V-NMR spectroscopy have been used to study the reactions occurring between bisperoxo vanadates and a number of histidine and histidine-like ligands, in aqueous alcoholic solutions. Coordination of one and two molecules of ligand is observed with all the compounds investigated affording [VO5L]- and [VO52L]-, respectively. Characterization of these species has been achieved by MSn experiments, which have allowed specific fragmentations of the peroxidic moiety to be distinguished. In particular, with [VO52L]-, two distinct modes of decomposition were observed, depending on the presence in the ligand of a free carboxylic function. - Possible biochemical implications related to vanadium haloperoxidase enzymes are discussed.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 1193-1197 
    ISSN: 1434-1948
    Keywords: Peroxo complexes ; Vanadium ; Mass spectrometry ; Ion-molecule reactions ; Ab initio calculations ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Electrospray Ionization Mass Spectrometry (ESI-MS) measurements and ab initio calculations on [OV(O2)(H2O)m-(CH3OH)n]+ (m,n: 0-4) peroxo cations have been carried out. This experimental technique allowed the direct observation of the above mentioned species for the first time. The results obtained clearly indicate that the exchange reactions between water and methanol molecules, within the coordination sphere of monoperoxo-vanadium complexes, is a conceivable and fast process.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 329-336 
    ISSN: 0894-3230
    Keywords: Chemistry ; Theoretical, Physical and Computational Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The oxidation of organic compounds by hydrogen peroxide, catalysed by transition metal derivatives, e.g. V(V), Mo(VI) and W(VI) complexes, involves the formation of peroxometal complexes. These are much more efficient oxidants than hydrogen peroxide so that the catalysed reactions are of remarkable synthetic significance. Several peroxometal complexes can be isolated and used as stoichiometric oxidants. An appealing feature of these oxidants is their versatility, as demonstrated by the fact that they are able to oxidize substrates such as alkenes, alcohols, ketones, sulphur, phosphorus and nitrogen derivatives and even aromatic and aliphatic hydrocarbons. Either polar or radical oxidations may take place. The reactivity depends on the nature of the metal and especially on the nature of the ligands coordinated to the metal. Therefore, an important goal consists in predicting the reactivity of peroxometal complexes on the basis of their structural features. Examples presented demonstrate that structure-reactivity correlations may be established. However, the effect of the ligands appears to be complex so that care must be exercised in drawing general conclusions.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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