Tuneable and degradable thermosets possessing dynamic aliphatic disulfide bonds via stereoselective thiol-yne polymerisation

Abstract

The permanent chemical structure that makes thermosets strong and stretchable materials also hinders their reprocessability and leads to their accumulation in the environment. To favour material reprocessability and reuse, polymers have been endowed with dynamic covalent bonds. However, when the dynamic bond is the network-forming bond, a significant trade-off between the robustness of the material and the dynamic behaviour can be encountered. In this study, nucleophilic thiol-yne click polymerisation was used to synthesise different materials possessing tuneable amounts of reversible disulfide bonds, thus achieving diverse thermomechanical properties. Furthermore, by leveraging different catalyst systems, the cis/trans conformer ratio on the backbone could be modulated to provide an additional degree of control over the thermomechanical properties. Finally, the presence of dynamic bonds was used as a handle to enable promotion of degradation and material reprocessing.

Supplementary files

Transparent peer review

To support increased transparency, we offer authors the option to publish the peer review history alongside their article.

View this article’s peer review history

Article information

Article type
Paper
Submitted
23 Okt. 2024
Accepted
20 Dec. 2024
First published
20 Dec. 2024
This article is Open Access
Creative Commons BY license

Polym. Chem., 2024, Accepted Manuscript

Tuneable and degradable thermosets possessing dynamic aliphatic disulfide bonds via stereoselective thiol-yne polymerisation

D. Giannantonio, A. Brandolese and A. P. Dove, Polym. Chem., 2024, Accepted Manuscript , DOI: 10.1039/D4PY01195C

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements