Star Polymer Network Elastomer with Reconfigurable Network Structure via Covalent Bond Exchange through Olefin Metathesis
A covalent adaptable network (CAN) elastomer with a well-defined network structure was fabricated by end-linking monodisperse star polymers via associative dynamic covalent bonds (DCBs). Monodisperse 4-arm star-shaped polyesters with vinyl end groups were synthesized and end-linked by an olefin metathesis reaction, yielding an elastomer with a uniform chain length between cross-links. The well-defined network structure endowed the elastomer with good mechanical properties. The remaining C═C bonds in the network could exchange via olefin metathesis, rendering the network structure reconfigurable. As a result, the elastomer showed stress relaxation and was thermally reprocessable. Moreover, the elastomer was chemically degradable into un-cross-linked polymers under mild conditions through C═C bond exchange. This study demonstrates mechanical robustness and dynamicity in rubbery materials through the combination of a well-defined network structure and associative DCBs.
Authors
- Naoko Yoshie (ORCID: https://orcid.org/0000-0002-9473-3226)
- Shintaro Nakagawa (ORCID: https://orcid.org/0000-0002-9848-2823)
- Ryo Sasaki (ORCID: https://orcid.org/0000-0002-2652-5097)
Institutions
- The University of Tokyo (JP)
Publication Details
- Journal
- ACS Macro Letters
- Published
- 2025-04-02
- DOI
- https://doi.org/10.1021/acsmacrolett.5c00135
- Citations
- 6
- Primary Topic
- Synthetic Organic Chemistry Methods
- Type
- article
- Field-Weighted Citation Impact
- 5.62
Funders
- Tokuyama Science Foundation
- Japan Society for the Promotion of Science