Back to Search
Start Over
Synthesis of Main-Chain Poly(fullerene)s from a Sterically Controlled Azomethine Ylide Cycloaddition Polymerization
- 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.
- Subjects :
- Steric effects
chemistry.chemical_classification
Fullerene
Polymers and Plastics
Organic Chemistry
Azomethine ylide
02 engineering and technology
Polymer
010402 general chemistry
021001 nanoscience & nanotechnology
01 natural sciences
Cycloaddition
0104 chemical sciences
Inorganic Chemistry
chemistry.chemical_compound
Monomer
chemistry
Polymerization
Polymer chemistry
Materials Chemistry
[CHIM]Chemical Sciences
0210 nano-technology
Macromolecule
Subjects
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⟩