| Literature DB >> 25893009 |
Maciej Podgórski1, Eftalda Becka2, Shunsuke Chatani2, Mauro Claudino2, Christopher N Bowman2.
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.Entities:
Keywords: DMA; hydrolytic degradation; thiol-Michael reaction; thiol-ene reaction
Year: 2015 PMID: 25893009 PMCID: PMC4397656 DOI: 10.1039/C4PY01552E
Source DB: PubMed Journal: Polym Chem ISSN: 1759-9954 Impact factor: 5.582