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  • Articles: DFG German National Licenses  (3)
  • 1990-1994  (3)
  • Chemistry  (3)
  • Aristotelia chilensis
  • Luminol luminescence induced by luminol
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  • Articles: DFG German National Licenses  (3)
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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 1649-1655 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The photoinitiation efficiency of the fluorenone/triethylamine (TEA) system in the polymerization of methylmethacrylate (MMA) has been evaluated as a function of the monomer concentration, the amine concentration, and the polarity of the reaction medium. The polymerization proceeds readily in low polarity media (benzene/monomer), but it is negligible in more polar solvents (acetonitrile/monomer). The polymerization rate increases with the amine concentration up to 0.01 M TEA. Further increase in amine concentration produces a decrease in the polymerization rate. A similar behavior was observed for the fluorenone photoreduction yield and the yield of fluorenone derived radicals. All these processes are considered to involve the excited triplet, while quenching of the excited singlet by the amine decreases the rate of these processes. However, the decrease in photoinitiation efficiency observed at high amine concentration is larger than that expected from the singlet quenching extent, as estimated from the effect of the amine on the fluorescence yield under the same experimental conditions. This discrepancy indicates that other process(es) must contribute to the protection afforded by high amine concentrations. Quenching of the charge transfer intermediate by the amine is postulated as a competitive process that could explain the above mentioned effects. © 1994 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 2465-2474 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Addition of triethylamine (TEA) notably increases the efficiency of anthraquinone (AQ) as photoinitiator of methyl methacrylate (MMA) free radical polymerization in nonpolar solvents. On the other hand, when alcohols or acetonitrile are employed as solvents the addition of TEA decreases the AQ photoinitiated polymerization rate. The polymerization efficiency measured in nonpolar solvents decreases when the MMA concentration increases. These results are explained in terms of quenching of the AQ-TEA charge transfer complex by MMA. This conclusion is supported by the decrease in AQ photoconsumption and AQH2 formation produced by the monomer addition.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 23 (1991), S. 761-766 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Tert-butoxyl radicals react with indole and methyl substituted derivatives by hydrogen abstraction. For those compounds which are unsubstituted at the N-atom, hydrogen abstraction takes place almost exclusively at the N—H bond. The reactivity of these compounds correlates with their donor electron capacity, pointing to significant contribution of charge transfer to the transition state stability. Substitution at the N atom considerably decreases the reactivity.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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