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

Balta, Demet; Bagdatli, Emine; ARSU, Nergis; Ocal, Nuket; Yagci, Yusuf

doi:10.1016/j.jphotochem.2007.11.009

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

Atıf İçin Kopyala

Balta D. K., Bagdatli E., ARSU N., Ocal N., Yagci Y.

JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, cilt.196, sa.1, ss.33-37, 2008 (SCI-Expanded)

Yayın Türü: Makale / Tam Makale
Cilt numarası: 196 Sayı: 1
Basım Tarihi: 2008
Doi Numarası: 10.1016/j.jphotochem.2007.11.009
Dergi Adı: JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY
Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
Sayfa Sayıları: ss.33-37
İstanbul Teknik Üniversitesi Adresli: Evet

Özet

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.