Thiol–ene grafting from polylactic acid, ...
Document type :
Article dans une revue scientifique: Article original
Permalink :
Title :
Thiol–ene grafting from polylactic acid, polycaprolactone, and polyhydroxybutyrate
Author(s) :
Belkhir, Kedafi [Auteur]
Ingénierie des Matériaux Polymères [IMP]
Jegat, Corinne [Auteur]
Ingénierie des Matériaux Polymères [IMP]
Taha, Mohamed [Auteur]
Ingénierie des Matériaux Polymères [IMP]
Ingénierie des Matériaux Polymères [IMP]
Jegat, Corinne [Auteur]
Ingénierie des Matériaux Polymères [IMP]
Taha, Mohamed [Auteur]
Ingénierie des Matériaux Polymères [IMP]
Journal title :
Reactive and Functional Polymers
Abbreviated title :
Reactive and Functional Polymers
Volume number :
101
Pages :
82-89
Publisher :
Elsevier BV
Publication date :
2016-04
ISSN :
1381-5148
English keyword(s) :
Thiol–ene reactions
Active monomers
Functional polymers
Acrylate methacrylate addition
Chain transfer constant
Active monomers
Functional polymers
Acrylate methacrylate addition
Chain transfer constant
HAL domain(s) :
Chimie/Polymères
Chimie/Matériaux
Chimie/Matériaux
English abstract : [en]
Thiol–ene additions of different monomers from multi-thiol functionalized biodegradable polymers are analyzed in this study. These monomers include quaternary ammonium groups known for their biological activities; and also ...
Show more >Thiol–ene additions of different monomers from multi-thiol functionalized biodegradable polymers are analyzed in this study. These monomers include quaternary ammonium groups known for their biological activities; and also methyl methacrylate (MMA) and hydroxyethyl methacrylate (HEMA), which are used to control the hydrophilic–hydrophobic balance in the issued copolymers. Monomer conversion and the resulting polymer structures are confirmed principally by 1H nuclear magnetic resonance (NMR) spectra. Model reactions are first conducted with thiophenol, and then polylactic acid (PLA), polycaprolactone (PCL), and polyhydroxybutyrate (PHB) multi-thiol functionalized polymers are successfully used. The structures of the obtained products are analyzed by 1H NMR spectra: all the reactions are kinetically controlled and monomer additions are controllable. Chain transfer constants of the used monomers to the multi-thiol functionalized PLA are between 1.4 and 1.9. The obtained products were also characterized by size-exclusion chromatography (SEC), differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA).Show less >
Show more >Thiol–ene additions of different monomers from multi-thiol functionalized biodegradable polymers are analyzed in this study. These monomers include quaternary ammonium groups known for their biological activities; and also methyl methacrylate (MMA) and hydroxyethyl methacrylate (HEMA), which are used to control the hydrophilic–hydrophobic balance in the issued copolymers. Monomer conversion and the resulting polymer structures are confirmed principally by 1H nuclear magnetic resonance (NMR) spectra. Model reactions are first conducted with thiophenol, and then polylactic acid (PLA), polycaprolactone (PCL), and polyhydroxybutyrate (PHB) multi-thiol functionalized polymers are successfully used. The structures of the obtained products are analyzed by 1H NMR spectra: all the reactions are kinetically controlled and monomer additions are controllable. Chain transfer constants of the used monomers to the multi-thiol functionalized PLA are between 1.4 and 1.9. The obtained products were also characterized by size-exclusion chromatography (SEC), differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA).Show less >
Language :
Anglais
Peer reviewed article :
Oui
Audience :
Internationale
Popular science :
Non
Administrative institution(s) :
Université de Lille
CNRS
INRA
ENSCL
CNRS
INRA
ENSCL
Collections :
Submission date :
2021-11-02T15:38:35Z
2021-11-05T07:51:42Z
2021-11-08T10:24:19Z
2021-11-05T07:51:42Z
2021-11-08T10:24:19Z