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- W2317446656 abstract "Selective polymerization of glycidyl methacrylate (GMA), which has two polymerizable functional groups such as epoxide and methacrylate, was achieved by the monomer-activated anionic approach using tetraoctylammonium bromide/triisobutylaluminum initiating system in toluene at 20 °C. Quantitative and controlled synthesis of poly(glycidyl methacrylate ether), up to about 20 000 g/mol, with pendant methacrylate functions, was obtained by ring-opening of the epoxide. The copolymerization of glycidyl methacrylate with glycidyl methyl ether (GME) in similar conditions, the resulting copolyether structures, and their properties were investigated as a function of feed composition. Reactive poly(glycidyl methyl ether-co-glycidyl methacrylate ether)s P(GME-co-GMA) with lower critical solubility temperature depending on the ratio [GME]/[GMA] were prepared and analyzed by NMR spectroscopy and differential scanning calorimetry. Postpolymerization cross-linking reactions of PGMA and random P(GME-co-GMA) copolymers were investigated by infrared spectroscopy and water contact angle measurements under heating or UV irradiation." @default.
- W2317446656 created "2016-06-24" @default.
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- W2317446656 date "2011-07-26" @default.
- W2317446656 modified "2023-10-14" @default.
- W2317446656 title "Selective Ring-Opening Polymerization of Glycidyl Methacrylate: Toward the Synthesis of Cross-Linked (Co)polyethers with Thermoresponsive Properties" @default.
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- W2317446656 doi "https://doi.org/10.1021/ma201075n" @default.
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