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Photoinitiating free-radical polymerization electron-transfer pairs applying amino acids and sulfur-containing amino acids as electron donors

Authors

  • Franciszek ścigalski,

    Corresponding author
    1. Faculty of Chemical Technology and Engineering, University of Technology and Agriculture, Seminaryjna 3, 85-326 Bydgoszcz, Poland
    • Faculty of Chemical Technology and Engineering, University of Technology and Agriculture, Seminaryjna 3, 85-326 Bydgoszcz, Poland
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  • Jerzy Pączkowski

    1. Faculty of Chemical Technology and Engineering, University of Technology and Agriculture, Seminaryjna 3, 85-326 Bydgoszcz, Poland
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Abstract

A series of free-radical polymerization initiation systems, based on xanthene dyes as the absorbing chromophores [Rose bengal derivative, 3-(3-methylbutoxy)-5,7-diiodo-6-fluorone and 3-acetoxy-2,4,5,7-tetraiodo-6-fluorone] and sulfur-containing amino acids as the electron donors, were investigated. The photoredox pair xanthene dye/sulfur-containing amino acid was effectively used for photoinitiation of free-radical polymerization of the mixture composed of poly(ethylene glycol)diacrylate–1% NH4OH (3 : 1). The highest initiating efficiencies were observed for the system composed of methionine derivatives as the electron donor. The mechanism of photoinduced electron transfer between sulfur-containing amino acids and triplet state of xanthene dye was investigated using laser-flash and steady-state photolysis techniques. Based on photochemistry of xanthene dyes, photochemistry of sulfur-containing amino acids, and obtained results, the mechanism describing the major processes occurring during the photoinitiated polymerization by a photoinduced intermolecular electron-transfer process was postulated. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 97: 358–365, 2005

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