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We report a straightforward and scalable method for the generation of polystyrene-based vinylogous urethane vitrimers using conventional radical polymerization. The copolymerization of the commercially available and inexpensive monomers styrene and (2-acetoacetoxy)ethyl methacrylate produced β-ketoester-functional network precursors on a multigram scale, which could be cross-linked with diamines to yield thermally robust vitrimer materials. Vitrimers were (re)processed over three destruction/compression cycles with acid catalysis to overcome the effects of backbone entanglements. Lastly, the viscoelastic properties were investigated, revealing a higher activation energy for viscous flow (Ea) compared with previously prepared methacrylate-based analogs.
Lessard et al. (Thu,) studied this question.