Facile synthesis of 1,4-cis-polyisoprene–polypeptide hybrids with different architectures

Autor: Amélie Vax, Frédéric Peruch, François Jean-Baptiste-Dit-Dominique, Jérémie Grange, Stéphane Grelier, Alexei V. Radchenko, Rachid Matmour
Přispěvatelé: Team 1 LCPO : Polymerization Catalyses & Engineering, Laboratoire de Chimie des Polymères Organiques (LCPO), Centre National de la Recherche Scientifique (CNRS)-Institut Polytechnique de Bordeaux-Ecole Nationale Supérieure de Chimie, de Biologie et de Physique (ENSCBP)-Université de Bordeaux (UB)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Institut Polytechnique de Bordeaux-Ecole Nationale Supérieure de Chimie, de Biologie et de Physique (ENSCBP)-Université de Bordeaux (UB)-Institut de Chimie du CNRS (INC), Société Michelin, Team 2 LCPO : Biopolymers & Bio-sourced Polymers
Rok vydání: 2019
Předmět:
Zdroj: Polymer Chemistry
Polymer Chemistry, Royal Society of Chemistry-RSC, 2019, 10 (19), pp.2456-2468. ⟨10.1039/c9py00241c⟩
ISSN: 1759-9962
1759-9954
DOI: 10.1039/c9py00241c
Popis: International audience; The synthesis of polypeptide hybrids by controlled/living ring-opening polymerization of N-carboxyanhydrides (NCA) using Schreiner′s thiourea catalyst and amino-alcohol terminated poly(1,4-cis-isoprene)s as initiators was demonstrated for γ-benzyl-ʟ-glutamate (BLG) and ε-tert-butyloxycarbonyl-ʟ-lysine (BLL) NCAs. One-pot synthesis of amino-alcohol terminated macroinitiators from heterotelechelic keto/aldehyde polyisoprene by reductive amination of carbonyl(s) was presented. Selection of amines allowed to obtain mono-, di-and tri-functional macroinitiators that were used for the synthesis of polyisoprene-polypeptide hybrids of different architecture: AB, BAB, AB2, BAB2, CBABC. Due to the living character of the polymerization, the molar mass of the polypeptide blocks could be controlled by the monomer to initiator ratio (6000
Databáze: OpenAIRE