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Syntheses of 12‐arm star polymers and star diblock copolymers by nitroxide‐mediated radical polymerization using dendritic dodecafunctional macroinitiators
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2005
Year
Macromolecular ChemistryEngineeringDendritic Dodecafunctional MacroinitiatorsOrganic ChemistryNitroxide‐mediated Radical PolymerizationChemistryTempo‐mediated Radical PolymerizationPolymersChemical EngineeringBenzyl AlcoholMacromolecular EngineeringPolymer ProcessingStar PolymersStar Diblock CopolymersPolymer ChemistrySynthetic MacromoleculeBiomolecular EngineeringPolymer SciencePolymer CharacterizationPolymerization KineticsPolymer ReactionPolymer Synthesis
Abstract Dendritic multifunctional macroinitiators having 12 TEMPO‐based alkoxyamines were prepared by the reaction of a benzyl alcohol having 4 TEMPO‐based alkoxyamines with 1,3,5‐tris[(4‐chlorocarbonyl)phenyl]benzene and 1,3,5‐tris(4‐isocyanatophenyl)benzene. Using the dodecafunctional macroinitiators, TEMPO‐mediated radical polymerizations of styrene (St) were carried out at 120 °C, and 12‐arm star polymers ( star‐12 ) with narrow polydispersities of M w / M n = 1.06–1.26 were obtained. To evaluate the livingness for the TEMPO‐mediated radical polymerizations of St, hydrolysis of the ester bonds of the 12‐arm star polymers and subsequent SEC measurements were carried out. Furthermore, using star‐12 as the macroinitiator, TEMPO‐mediated radical polymerization of 4‐vinylpyridine (4‐VP) was carried out, and well‐defined poly(St)‐ b ‐poly(4‐VP) 12‐arm star diblock copolymers with M w / M n = 1.18–1.19 were obtained. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 3689–3700, 2005
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