| Literature DB >> 25289727 |
Lauren A Link1, Alexander T Lonnecker, Keith Hearon, Cameron A Maher, Jeffery E Raymond, Karen L Wooley.
Abstract
Polycarbonate networks derived from the natural product quinic acid that can potentially return to their natural building blocks upon hydrolytic degradation are described herein. Solvent-free thiol-ene chemistry was utilized in the copolymerization of tris(alloc)quinic acid and a variety of multifunctional thiol monomers to obtain poly(thioether-co-carbonate) networks with a wide range of achievable thermomechanical properties including glass transition temperatures from -18 to +65 °C and rubbery moduli from 3.8 to 20 MPa. The network containing 1,2-ethanedithiol expressed an average toughness at 25 and 63 °C of 1.08 and 2.35 MJ/m(3), respectively, and an order-of-magnitude increase in the average toughness at 37 °C of 15.56 MJ/m(3).Entities:
Keywords: photo-cross-linking; polycarbonates; quinic acid; renewable polymers; thiol−ene chemistry
Mesh:
Substances:
Year: 2014 PMID: 25289727 DOI: 10.1021/am506087e
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229