Synthesis and characterization of benzodioxinone mono-telechelics and their use in block copolymerization
Loading...
Date
2021-08-27
Authors
Journal Title
Journal ISSN
Volume Title
Publisher
Turkish Journal of Chemistry
Abstract
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.
Description
Keywords
Benzodioxinones, block copolymer, click chemistry, ketene chemistry, photoacylation