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  • Chemistry  (2)
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 16 (1984), S. 1623-1636 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of OH reactions with 1-4 carbon aliphatic thiols have been investigated over the temperature range 252-430 K. OH radicals were produced by flash photolysis of water vapor at λ 〉 165 nm and detected by time-resolved resonance fluorescence spectroscopy. All thiols investigated react with OH at nearly the same rate; k(298 K) = 3.2-4.6 × 10-11 cm3 molecule-1 s-1, -Eact = 0.6-1.0 kcal/mol, A = 0.6-1.2 × 10-11 cm3 molecule-1 s-1. CH3SH and CH3SD react with OH at identical rates over the entire temperature range investigated. We conclude that the dominant reaction pathway is addition to the sulfur atom.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 17 (1985), S. 303-313 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Rate coefficients for OH reactions with the 2-5 carbon aliphatic aldehydes have been measured under pseudo first-order conditions in OH. OH was generated by flash photolysis of H2O at wavelengths greater than 165 nm and its concentration monitored using time-resolved resonance fluorescence spectroscopy. Two reactions were studied only at 298 K while five reactions were studied over the temperature range 250-425 K; negative activation energies were observed for all five reactions. Aldehyde reactivity toward OH is nearly independent of the identity of the hydrocarbon side chain. Our results are compared with those obtained in previous studies of OH-aldehyde reaction kinetics and their mechanistic implications are discussed.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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