Chemical incorporation of thioxanthone into beta-cyclodextrin and its use in aqueous photopolymerization of methyl methacrylate


Balta D. , BAGDATLI E. , ARSU N. , OCAL N., Yağcı Y.

JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, vol.196, no.1, pp.33-37, 2008 (Journal Indexed in SCI) identifier identifier

  • Publication Type: Article / Article
  • Volume: 196 Issue: 1
  • Publication Date: 2008
  • Doi Number: 10.1016/j.jphotochem.2007.11.009
  • Title of Journal : JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY
  • Page Numbers: pp.33-37

Abstract

Photoinitiated free radical polymerization of methyl methacrylate(MMA) inaqueous solution via hydrogen abstraction mechanism was described. For this purpose, thioxanthone (TX) chromophoric group was chemically incorporated into beta-cyclodextrin (beta-CD) by a simple esterification process. The resulting thioxanthone photoinitiator (TX-beta-CD) exhibited similar spectral characteristics and photoactivity to that of the parent TX molecule. Host guest complexes of MMA with TX-beta-CD in water, in the presence of N-methyldiethanol amine (NMDEA) as a hydrogen donor, facilitated photoinitiated free radical polymerization in aqueous medium. The postulated mechanism is based on the intermolecular reaction of photoexcited triplet TX moiety of TX-beta-CD with NMDEA. The resulting amino alkyl radicals initiate the polymerization. (c) 2007 Elsevier B.V. All rights reserved.