Ester-free thiol-X resins: new materials with enhanced mechanical behavior and solvent resistance

Literature Information

Publication Date 2015-01-19
DOI 10.1039/C4PY01552E
Impact Factor 5.582
Authors

Eftalda Becka, Shunsuke Chatani, Mauro Claudino, Christopher N. Bowman


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Abstract

A series of thiol-Michael and radical thiol–ene network polymers were successfully prepared from ester-free as well as ester-containing monomer formulations. Polymerization reaction rates, dynamic mechanical analysis, and solvent resistance experiments were performed and compared between compositions with varied ester loading. The incorporation of ester-free alkyl thiol, vinyl sulfone and allylic monomers significantly improved the mechanical properties when compared with commercial, mercaptopropionate-based thiol–ene or thiol-Michael networks. For polymers with no hydrolytically degradable esters, glass transition temperatures (Tg's) as high as 100 °C were achieved. Importantly, solvent resistance tests demonstrated enhanced stability of ester-free formulations over PETMP-based polymers, especially in concentrated basic solutions. Kinetic analysis showed that glassy step-growth polymers are readily formed at ambient conditions with conversions reaching 80% and higher.

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Polymer Chemistry
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