Synthesis of a transesterification vitrimer activated by fluorine from an α,αdifluoro carboxylic acid and a diepoxy
Abstract
An α,α-difluorodicarboxylic acid (P-DAF) was easily synthesized in two steps from diiodobenzene and reacted with a commercial diepoxy (BDGE). The electron-withdrawing effect of the fluorinated group activated the polymerization and gelation readily happened at room temperature. After curing at 150 °C a novel dynamic material was obtained. The P-DAF/BDGE material exhibited a high gel content (94 %) and was able to flow when heated. This material could be successfully reshaped by compression molding under mild conditions (1.5 h at 150 °C). This new material demonstrates that catalyst-free transesterification vitrimers can be prepared from difunctional monomers.
Domains
Polymers| Origin | Files produced by the author(s) |
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