Unsaturated polyurethanes degradable by conjugate substitution reactions with amines and carboxylate anions.

ABSTRACT: Main-chain scission of polymers induces a significant decrease in molecular weight and accompanying changes in physical properties and is important for applications in materials engineering, such as in photoresists and adhesive dismantling. In this study, we focused on methacrylates substituted with carbamate groups at the allylic positions for the purpose of developing a mechanism that efficiently cleaves the main chain in response to chemical stimuli. Dimethacrylates substituted with hydroxy groups at the allylic positions were synthesized by the Morita-Baylis-Hillman reaction of diacrylates and aldehydes. The polyaddition with diisocyanates afforded a series of poly(conjugated ester-urethane)s. These polymers underwent a conjugate substitution reaction with diethylamine or acetate anion

SUBMITTER: Noda T 

PROVIDER: S-EPMC10327625 | biostudies-literature | 2023 Jun

REPOSITORIES: biostudies-literature