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Tertiary amine-functionalized polymers by atom transfer radical polymerization

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dc.contributor.author Summers G.J. en
dc.contributor.author Patrick Ndawuni M. en
dc.contributor.author Summers C.A. en
dc.date.accessioned 2012-11-01T16:31:38Z
dc.date.available 2012-11-01T16:31:38Z
dc.date.issued 2001 en
dc.identifier.citation Journal of Polymer Science, Part A: Polymer Chemistry en
dc.identifier.citation 39 en
dc.identifier.citation 12 en
dc.identifier.issn 0887624X en
dc.identifier.other 10.1002/pola.1182 en
dc.identifier.uri http://hdl.handle.net/10500/7490
dc.description.abstract The quantitative synthesis of tertiary amine-functionalized polymers by atom transfer radical polymerization is reported. Tertiary amine-functionalized polystyrene was prepared with the adduct of 1-(bromoethyl)benzene with 1-(4-dimethyl-aminophenyl)-1-phenylethylene as an initiator in the atom transfer radical polymerization of styrene in the presence of a copper (I) bromide/2,2′-bipyridyl catalyst system. The polymerization proceeded via a controlled free-radical polymerization process to afford quantitative yields of the corresponding tertiary amine-functionalized polystyrene with predictable number-average molecular weights (1600-4400), narrow molecular weight distributions (1.09-1.31), and an initiator efficiency of 0.95. The polymerization process was monitored by gas chromatographic analysis. The tertiary amine-functionalized polymers were characterized by thin-layer chromatography, size exclusion chromatography, potentiometry, and spectroscopy. All experimental evidence was consistent with quantitative functionalization via the 1,1-diphenylethylene derivative. Polymerization kinetic measurements showed that the polymerization reaction followed first-order-rate kinetics with respect to monomer consumption and that the number-average molecular weight increased linearly with monomer conversion. en
dc.language.iso en en
dc.subject 1,1-diphenylethylenes; Amination; Atom transfer radical polymerization; Functionalization; Functionalized polystyrene; Telechelic polymers; Tertiary amine groups Amination; Functional polymers; Gas chromatography; Initiators (chemical); Molecular weight distribution; Organic polymers; Polystyrenes; Size exclusion chromatography; Spectroscopic analysis; Styrene; Synthesis (chemical); Thin layer chromatography; Atom transfer radical polymerization; Diphenylethylenes; Functionalization; Functionalized polystyrene; Telechelic polymers; Tertiary amine group; Free radical polymerization en
dc.title Tertiary amine-functionalized polymers by atom transfer radical polymerization en
dc.type Article en


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