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Controlled synthesis of new amphiphilic glycopolymers with liquid crystal grafts
Authors:Khalid Ferji  Cécile Nouvel  Jérôme Babin  Pierre‐Antoine Albouy  Min‐Hui Li  Jean‐Luc Six
Affiliation:1. Laboratoire de Chimie Physique Macromoléculaire LCPM, Université de Lorraine, , Nancy, F‐54000 France;2. Laboratoire de Chimie Physique Macromoléculaire LCPM, , Nancy, F‐54000 France;3. Laboratoire de Physique des Solides, Université Paris‐Sud, , F‐91405 Orsay Cedex, France;4. Institut Curie, CNRS, Laboratoire Physico‐Chimie Curie, Université Pierre et Marie Curie, , F‐75248 Paris cedex 05, France
Abstract:A cholesterol‐based liquid crystal monomer, diethylene glycol cholesteryl ether acrylate (DEGCholA), has been successfully polymerized by atom transfer radical polymerization (ATRP) for the first time. Appropriate experimental conditions to control the polymerization of DEGCholA have been investigated using a model initiator (ethyl 2‐bromoisobutyrate) in tetrahydrofuran (THF) or toluene at 60 °C. Well‐controlled ATRP of DEGCholA was obtained using N,N,N′,N′,N″‐pentamethyldiethylenetriamine as ligand in THF at 60 °C. These conditions were then applied to initiate the ATRP of DEGCholA from multifunctional macroinitiators based on dextran. Using a protection/deprotection synthetic scheme, novel graft glycopolymers (Dex‐g‐PDEGCholA) have been synthesized. The mesomorphic properties of DEGCholA, PDEGCholA, and Dex‐g‐PDEGCholA have been studied by thermal polarizing optical microscopy, differential scanning calorimetry, and X‐ray scattering. PDEGCholA and Dex‐g‐PDEGCholA show an interdigitated smectic A phase (SmAd) between Tg (~30 °C) and around 170 °C. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013 , 51, 3829–3839
Keywords:amphiphilic  atom transfer radical polymerization (ATRP)  cholesterol  dextran  glycopolymer  graft copolymers  liquid crystal copolymer  polysaccharides
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