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Direct one-pot synthesis of poly(ionic liquid) nanogels by cobalt-mediated radical cross-linking copolymerization in organic or aqueous media

Authors :
Daniel Taton
Daniela Cordella
Mathilde Weiss-Maurin
Christophe Detrembleur
Christine Jérôme
Univ Liege, Dept Chem, CERM
Université de Liège-CERM
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)
Team 1 LCPO : Polymerization Catalyses & Engineering
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)
Source :
Polymer Chemistry, Polymer Chemistry, Royal Society of Chemistry-RSC, 2016, 7 (14), pp.2521-2530. ⟨10.1039/c6py00112b⟩
Publication Year :
2016
Publisher :
Royal Society of Chemistry (RSC), 2016.

Abstract

International audience; Nanogels of controlled kinetic chain length were synthesized by cobalt-mediated radical cross-linking copolymerization (CMRccP) involving a vinyl monomer and a divinyl cross-linker. This strategy was first validated to achieve neutral poly(vinyl acetate) nanogels by CMRccP of vinyl acetate and divinyl adipate as a cross-linker at 40 degrees C in the presence of an alkyl-cobalt(III) serving both as an initiator and a controlling agent using ethyl acetate as a solvent. Poly(ionic liquid) nanogels were then directly obtained by CMRccP of N-vinyl-3-ethyl imidazolium bromide in the presence of 1,13-divinyl-3-decyl diimidazolium bromide as a cross-linker. CMRccP experiments could be conducted either in an organic solvent using dimethyl formamide or, more interestingly, in aqueous solution, demonstrating the robustness and versatility of this one-step process. Chain extensions of PIL nanogels were also carried out in water, forming core-shell structures, thus opening new avenues in the design of functional nanogels.

Details

ISSN :
17599962 and 17599954
Volume :
7
Database :
OpenAIRE
Journal :
Polymer Chemistry
Accession number :
edsair.doi.dedup.....b0d947ddb962c8c3c81222d936a8d18f