Thiol–ene grafting from polylactic acid, ...
Type de document :
Article dans une revue scientifique: Article original
URL permanente :
Titre :
Thiol–ene grafting from polylactic acid, polycaprolactone, and polyhydroxybutyrate
Auteur(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]
Titre de la revue :
Reactive and Functional Polymers
Nom court de la revue :
Reactive and Functional Polymers
Numéro :
101
Pagination :
82-89
Éditeur :
Elsevier BV
Date de publication :
2016-04
ISSN :
1381-5148
Mot(s)-clé(s) en anglais :
Thiol–ene reactions
Active monomers
Functional polymers
Acrylate methacrylate addition
Chain transfer constant
Active monomers
Functional polymers
Acrylate methacrylate addition
Chain transfer constant
Discipline(s) HAL :
Chimie/Polymères
Chimie/Matériaux
Chimie/Matériaux
Résumé en anglais : [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 ...
Lire la suite >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).Lire moins >
Lire la suite >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).Lire moins >
Langue :
Anglais
Comité de lecture :
Oui
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
Université de Lille
CNRS
INRA
ENSCL
CNRS
INRA
ENSCL
Collections :
Date de dépôt :
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