Demonstrates effective polymerization using a bifunctional monomer from isoeugenol, suggesting sustainable polymer materials.
There has been a growing movement to effectively utilize phenylpropanoids as biomass resources for polymer materials in pursuit of a sustainable society.Isoeugenol, an aromatic biomass resource, is expected to be a sustainable polymer feedstock from the viewpoint of availability and price.On the other hand, due to its -substituted styrene structure, it has poor reactivity in cation/radical polymerization and is difficult to polymerize on its own.In this study, we focused on catalytic [3 + 2] cycloaddition reactions of isoeugenol and utilized it for polymerization.Specifically, we designed a bifunctional monomer consisting of two isoeugenol molecules bonded by silicon to achieve efficient polymerization using catalytic [3 + 2] cycloaddition reactions.Furthermore, the polymer was decomposable under mild conditions, and the decomposition products were suitable for chemical recycling and upcycling.
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Nagaya et al. (2026) studied this question.
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