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Updated: Jan 12, 2026

Synthesis of Information-bearing Peptoids and their Sequence-directed Dynamic Covalent Self-assembly
Published on: February 6, 2020
Dynamic β-Amino Sulfonamides for the Synthesis of Covalent Adaptable Networks
Stephan Maes1, Loc Tan Nguyen1, Johan M Winne1
1Polymer Chemistry Research group, Centre of Macromolecular Chemistry (CMaC) and Laboratory of Organic Synthesis, Department of Organic and Macromolecular Chemistry, Faculty of Sciences, Ghent University, Krijgslaan 291, Ghent, 9000, Belgium.
Abstract:
Thermosets are indispensable for their lightweight and excellent thermomechanical properties but suffer from nonrecyclability, exacerbating plastic pollution. Covalent Adaptable Networks (CANs), leveraging dynamic covalent bonds, address this challenge. This study explores β-amino sulfonamides (BASA) as novel dynamic and thermoreversible linkers for CANs. Compared to previously investigated β-amino amides (BAAs), small molecule BASA studies show a faster amine exchange reaction via (retro)aza-Michael reactions in a temperature window from 140 to 180 °C. More importantly, in contrast to the acrylamide monomers released from BAAs, the vinyl sulfonamide monomers released from BASAs are more robust and can resist homopolymerization at elevated temperatures. We showed that bisfunctional vinyl sulfonamide cross-linkers enable the synthesis of CANs with tunable properties, as verified through thermomechanical and rheological analysis. The anticipated increased thermal stability of BASA-based CANs was shown by the retention of mechanical and rheological performance over at least five recycling cycles.
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