Macromolecules · 2007 · 160 citations · 17 references
Natural SciencesChemistryMaterials ScienceOrganic ChemistryPolymer ChemistryPolymer MaterialsPolymer CharacterizationPolymer ProcessingPolymer SynthesisPolymerization ChemistryPolymerization ProcessesControlled PolymerizationControlled Radical PolymerizationLiving Radical PolymerizationNitroxide-mediated PolymerizationNumber-average Molecular WeightPolymer Polydispersity AnalysisPolymerization ReactionsSize-exclusion Liquid Chromatography
Bulk methyl methacrylate (MMA) controlled radical polymerization was carried out using two 2,2-diphenyl-3-phenylimino-2,3-dihydroindol-1-yloxyl nitroxide (DPAIO) based alkoxyamines. Whatever the alkoxyamine used, polymerization presents a controlled character, and high conversion can be reached. Polymerization up to 60% conversion, initiated with the nitro para-substituted alkoxyamine 2, showed a linear increase of number-average molecular weight ( M n ) vs conversion even at the beginning of the polymerization with the final polydispersity index (PDI) close to 1.4. A reinitiation test onto n -butyl acrylate has shown that even if this nitroxide is not suited for acrylate monomers, the shift of the size exclusion chromatography (SEC)trace proved the poly(methyl methacrylate)−DPAIO macroinitiator (PMMA−DPAIO) obtained had a living character. These results showed that the range of monomers that could be polymerized by nitroxide mediated polymerization (NMP) can still be extended.
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Kinetics of living radical polymerization
Atsushi Goto, Takeshi Fukuda · Progress in Polymer Science · 2004 · 890 citations
Didier Benoit, Sandra Grimaldi, Sophie Robin et al. · Journal of the American Chemical Society · 2000 · 402 citations · Full text
Bernadette Charleux, Julien Nicolas, Olivier Guerret · Macromolecules · 2005 · 236 citations