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Poly(thioether) Vitrimers via Transalkylation of Trialkylsulfonium Salts

Open access
Hendriks, Benjamin, Waelkens, Jelle, Winne, Johan M., Du Prez, Filip E.·2017·ACS Macro Letters

Abstract

Abstract Vitrimers are permanently cross-linked organic polymers that can be reshaped, molded, and recycled without loss of network integrity. Herein, we report poly(thioether) networks, prepared through a straightforward thiol–ene photopolymerization, that can be turned into catalyst-free vitrimer materials by partial alkylation of the thioethers (1–10%) to the corresponding trialkylsulfonium salts. Based on a classical SN2-type substitution, the resulting polyionic networks can be reshaped upon heating via swift transalkylation reactions. This novel exchange reaction for the design of vitrimers was studied both on low MW model compounds as well as on a material level. In addition, we demonstrated the recycling of these networks without significant loss of mechanical properties.

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Metadata

Authors
Hendriks, B., Waelkens, J., Winne, J. M., & Du Prez, F. E.
Venue
ACS Macro Letters
Published
2017-08-15
Volume
6
Issue
9
Pages
930-934
ISSN
2161-1653 (ISSN-L)
OpenAlex
W2750225980
Cited by
290
References
5
FWCI
15.88
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: Poly(thioether) Vitrimers via Transalkylation of Trialkylsulfonium Salts. https://app.cochat.ai/papers/10.1021/acsmacrolett.7b00494
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Hendriks, B., Waelkens, J., Winne, J. M., & Du Prez, F. E. (2017). Poly(thioether) Vitrimers via Transalkylation of Trialkylsulfonium Salts. ACS Macro Letters. https://doi.org/10.1021/acsmacrolett.7b00494

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