Incorporation of Thioacetate Pendants on a Polyalkenamer Enables High Extensibility

This study focuses on functionalizing polycyclooctene (PCOE) with thioacetate groups using thiol–ene click chemistry. The ethylene thioacetate (EVSA) copolymers produced vary in thioacetate incorporation (4–25 mol %) via a controlled semibatch addition technique with AIBN dosing. Copolymers with 4–1...

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Veröffentlicht in:Macromolecules 2024-11, Vol.57 (21), p.10358-10367
Hauptverfasser: John Chethalen, Roshni, Kim, Myounguk, Ruiz, Juan Correa, Tu, Chien-Hua, Gray, Jordan, Winey, Karen I., Lesser, Alan J., Crosby, Alfred J., Coughlin, E. Bryan
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Sprache:eng
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Zusammenfassung:This study focuses on functionalizing polycyclooctene (PCOE) with thioacetate groups using thiol–ene click chemistry. The ethylene thioacetate (EVSA) copolymers produced vary in thioacetate incorporation (4–25 mol %) via a controlled semibatch addition technique with AIBN dosing. Copolymers with 4–14 mol % thioacetate are semicrystalline, while those with 20–25 mol % are amorphous. Increased functionalization correlates with decreased crystallinity and increased stretchability, with the highest functionalization (25 mol %) showing a modulus of 0.045 MPa and 2000% elongation at break. This behavior is due to the pseudoprecise functionalization of the thioacetate pendants and intrinsic cross-linking that occurs during melt processing. Broadband dielectric spectroscopy (BDS) indicates a low activation energy barrier (16 kJ/mol for the β process), suggesting potential self-healing applications.
ISSN:0024-9297
1520-5835
DOI:10.1021/acs.macromol.4c02110