| Literature DB >> 28574160 |
Guillaume G Hedir1,2, Maria C Arno1, Marvin Langlais1, Jonathan T Husband1, Rachel K O'Reilly1, Andrew P Dove1.
Abstract
Polymers with a thermally triggered phase transition are important in the design of materials for biological applications, where their behavior can be used to trigger release or (dis)assembly events. Despite their advantages, a system with tunable thermal response, end-group reactive sites, low toxicity, and controlled main-chain degradability has not been realized, yet this would be a significant advance. The versatile new poly(oligo(ethylene glycol) vinyl acetate)s are presented with excellent control over their molecular properties obtained through RAFT/MADIX polymerization. Furthermore, we demonstrate structure-controlled thermal transitions, conjugation to human lysozyme through the retained end-group, and moreover show that this class of polymers can uniquely be copolymerized with 2-methylene-1,3-dioxepane (MDO) to generate polymers in which the degradability and cloud point can be independently tuned to create materials that display the same cloud point but degrade differently.Entities:
Keywords: biocompatibility; copolymerization; organocatalysis; polymerization; radical reactions
Year: 2017 PMID: 28574160 DOI: 10.1002/anie.201703763
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336