Repository logo
  • English
  • Català
  • Čeština
  • Deutsch
  • Español
  • Français
  • Gàidhlig
  • Italiano
  • Latviešu
  • Magyar
  • Nederlands
  • Polski
  • Português
  • Português do Brasil
  • Suomi
  • Svenska
  • Türkçe
  • Tiếng Việt
  • Қазақ
  • বাংলা
  • हिंदी
  • Ελληνικά
  • Yкраї́нська
  • Log In
    or
    Have you forgotten your password?
Repository logo
  • Communities & Collections
  • All of DSpace
  • English
  • Català
  • Čeština
  • Deutsch
  • Español
  • Français
  • Gàidhlig
  • Italiano
  • Latviešu
  • Magyar
  • Nederlands
  • Polski
  • Português
  • Português do Brasil
  • Suomi
  • Svenska
  • Türkçe
  • Tiếng Việt
  • Қазақ
  • বাংলা
  • हिंदी
  • Ελληνικά
  • Yкраї́нська
  • Log In
    or
    Have you forgotten your password?
  1. Home
  2. Browse by Author

Browsing by Author "Celik, Cumali"

Now showing 1 - 1 of 1
Results Per Page
Sort Options
  • Loading...
    Thumbnail Image
    Item
    Synthesis and characterization of benzodioxinone mono-telechelics and their use in block copolymerization
    (Turkish Journal of Chemistry, 2021-08-27) Celik, Cumali
    Poly (methyl methacrylate)(PMMA) and poly (ethylene glycol) methyl ether (mPEG)-based monotelechelics were quantitatively prepared by copper (I)-catalyzed azide/alkyne cycloaddition (CuAAC) click reactions using azido-terminated polymers and alkyne functional benzodioxinones. The monotelechelic containing dimethyl moities (2, 2-dimethyl-5-(prop-2-yn-1-yloxy)-4H-benzo [d][1, 3] dioxin-4-one) was heat-sensitive, whereas the monotelechelic containing diphenyl moieties (2, 2-diphenyl-5-(prop-2-yn-1-yloxy)-4H-benzo [d][1, 3] dioxin-4-one) was UV light sensitive. Based on the FT-IR, 1 H-NMR, and GPC investigations, the CuAAC click reactions enable the quantitative syntheses of monotelechelics under mild conditions. Moreover, the photosensitive mPEG-based monotelechelic was further utilized for the block copolymer synthesis upon UV-light irradiation. The photoinduced acylation of mPEG monotelechelic consist of (2, 2-diphenyl-5-(prop-2-yn-1-yloxy)-4H-benzo [d][1, 3] dioxin-4-one) in the presence of hydroxy-terminated poly (epsilon caprolactone) enabled the successful block copolymer formation.

DSpace software copyright © 2002-2025 LYRASIS

  • Cookie settings
  • Privacy policy
  • End User Agreement
  • Send Feedback