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.

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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

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article

Star Polymer Network Elastomer with Reconfigurable Network Structure via Covalent Bond Exchange through Olefin Metathesis

Naoko Yoshie, Shintaro Nakagawa, Ryo Sasaki
6 citations
ACS Macro Letters
Synthetic Organic Chemistry Methods
5.62
article

Star Polymer Network Elastomer with Reconfigurable Network Structure via Covalent Bond Exchange through Olefin Metathesis

Naoko Yoshie, Shintaro Nakagawa, Ryo Sasaki
article en
6 citations

Abstract

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.

ACS Macro LettersVol. 14(4)
The University of Tokyo (JP)
Tokuyama Science Foundation, Japan Society for the Promotion of Science
Openalex Percentile: Top 4%
Synthetic Organic Chemistry Methods
5.62
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