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Synthesis of Main-Chain Poly(fullerene)s from a Sterically Controlled Azomethine Ylide Cycloaddition Polymerization

Authors :
Hasina H. Ramanitra
Christine Dagron-Lartigau
Abdel Khoukh
Roger C. Hiorns
Simon Dowland
Didier Bégué
Craig Combe
Graham E. Morse
Carlos Frederico de Oliveira Graeff
Bruna Andressa Bregadiolli
Hugo Santos Silva
Andreas Distler
Instituto de Física
Universidade federal de uberlandia
Institut des sciences analytiques et de physico-chimie pour l'environnement et les materiaux (IPREM)
Université de Pau et des Pays de l'Adour (UPPA)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)
Source :
Macromolecules, Macromolecules, American Chemical Society, 2016, 49 (5), pp.1681--1691. ⟨10.1021/acs.macromol.5b02793⟩
Publication Year :
2016
Publisher :
HAL CCSD, 2016.

Abstract

International audience; Fullerene is used as a monomer in this simple method to prepare soluble, well-defined polymers. The sterically controlled azomethine ylide cycloaddition polymerization of fullerene (SACAP) yields macromolecules with molecular weights of around 25 000 g mol-1. Importantly, cumbersome comonomers are employed to restrict cross-linking. Extensive characterizations, with the help of modeling studies, indicate that the polymers are regio-irregular with a majority of trans-3 isomers. Of particular interest is the exceptional ease of preparing polymers with zero metal content. © 2016 American Chemical Society.

Details

Language :
English
ISSN :
00249297 and 15205835
Database :
OpenAIRE
Journal :
Macromolecules, Macromolecules, American Chemical Society, 2016, 49 (5), pp.1681--1691. ⟨10.1021/acs.macromol.5b02793⟩
Accession number :
edsair.doi.dedup.....cbda397a84125b95d4d106da2fe067b5
Full Text :
https://doi.org/10.1021/acs.macromol.5b02793⟩