Abstract
A vinyl ether bearing a carbonate side group (2-oxo-1,3-dioxolan-4-yl- methyl vinyl ether, GCVE) was synthesized and copolymerized with various commercially available fluoroolefins [chlorotrifluoroethylene (CTFE), hexafluoropropylene (HFP), and perfluoromethyl vinyl ether (PMVE)] by radical copolymerization initiated by tert-butyl peroxypivalate. Although HFP, PMVE, and vinyl ether do not homopolymerize under radical conditions, they copolymerized easily yielding alternating poly(GCVE-alt-F-alkene) copolymers. These alternating structures were confirmed by elemental analysis as well as 1H, 19F, and 13C NMR spectroscopy. All copolymers were obtained in good yield (73-85%), with molecular weights ranging from 3900 to 4600 g mol -1 and polydispersities below 2.0. Their thermogravimetric analyses under air showed decomposition temperatures at 10% weight loss (T d,10%) in the 284-330°C range. The HFP-based copolymer exhibited a better thermal stability than those based on CTFE and PMVE. The glass transition temperatures were in the 15-65°C range. These original copolymers may find potential interest as polymer electrolytes in lithium ions batteries. © 2012 Wiley Periodicals, Inc.
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Alaaeddine, A., Boschet, F., Ameduri, B., & Boutevin, B. (2012). Synthesis and characterization of original alternated fluorinated copolymers bearing glycidyl carbonate side groups. Journal of Polymer Science, Part A: Polymer Chemistry, 50(16), 3303–3312. https://doi.org/10.1002/pola.26112
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