Stereoregular functionalized polysaccharides via cationic ring-opening polymerization of biomass-derived levoglucosan.
Ontology highlight
ABSTRACT: We report the facile synthesis and characterization of 1,6-α linked functional stereoregular polysaccharides from biomass-derived levoglucosan via cationic ring-opening polymerization (cROP). Levoglucosan is a bicyclic acetal with rich hydroxyl functionality, which can be synthetically modified to install a variety of pendant groups for tailored properties. We have employed biocompatible and recyclable metal triflate catalysts - scandium and bismuth triflate - for green cROP of levoglucosan derivatives, even at very low catalyst loadings of 0.5 mol%. Combined experimental and computational studies provided key kinetic, thermodynamic, and mechanistic insights into the cROP of these derivatives with metal triflates. Computational studies reveal that ring-opening of levoglucosan deriva
SUBMITTER: Porwal MK
PROVIDER: S-EPMC9019921 | biostudies-literature | 2022 Apr
REPOSITORIES: biostudies-literature
ACCESS DATA