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  • Metal oxide Dissolution  (1)
  • Methylation  (1)
  • bromoalkyltriphenylphosphonium bromides  (1)
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 571-576 
    ISSN: 0268-2605
    Keywords: zerovalent metals ; bromoalkyltriphenylphosphonium bromides ; methylmercuric acetate ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Aqueous solutions of bromoalkyltriphenylphosphonium bromides react with zerovalent metals, causing their dissolution. The reaction initially follows second-order kinetics, with the rate depending on both metal and bromide concentrations. Zerovalent metals similarly react with aqueous methylmercuric acetate and other dissolved organometals. © 1998 John Wiley & Sons, Ltd.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 1 (1987), S. 545-554 
    ISSN: 0268-2605
    Keywords: Methylcobalamin (CH3B12) ; Metal oxides ; Methyl transfer ; Solid-surface reactions ; Metal oxide Dissolution ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Aqueous solutions of methylcobalamin (CH3B12) react with various water-insoluble metal oxides. The decomposition of methylcobalamin follows a kinetic pattern of two parallel first-order reactions. A proposed reaction mechanism involves the attachment of methylcobalamin to the oxide surface, followed by methyl transfer and dissolution of the oxide.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 3 (1989), S. 123-128 
    ISSN: 0268-2605
    Keywords: Methylation ; metals ; environment ; mobility ; cobalamin ; methyl iodide ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Formation of bonds between methyl groups and heavy elements (metals or metalloids) alters various physical properties such as solubility or volatility. This alteration enhances the mobility of the heavy metal and can play a major role in the environmental cycles for these elements. Environmental methylation has been established as a major factor in the environmental movement of mercury and arsenic, and very probably affects other elements similarly. Two methylating agents (methylcobalamin and methyl iodide) have been found to mobilize metals out of water-insoluble compounds and/or anoxic sediments. These two compounds react with quite different substrates, but the kinetics of the resulting dissolutions follow virtually identical patterns. These reactions proceed through formation of a methylated intermediate on the substrate surface, followed by movement of the heavy element out of the solid lattice into the surrounding solution.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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