Journal
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
Volume 43, Issue 14, Pages 2977-2984Publisher
WILEY
DOI: 10.1002/pola.20756
Keywords
amphiphiles; diblock copolymers; micelles; nitroxide-mediated polymerization
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Amphiphilic poly(ethylene oxide)-block-poly(isoprene) (PEO-b-PI) diblock copolymers were prepared by nitroxide-mediated polymerization of isoprene from alkoxyamine-terminal poly(ethylene oxide) (PEO). PEO monomethyl ether (M-n approximate to 5200 g/mol) was functionalized by esterification with 2-bromopropionyl bromide with subsequent copper-mediated replacement of the terminal bromine with 2,2,5-trimethyl-4-phenyl-3-azahexane-3-nitroxide. The resulting PEO-alkoxyamine macroinitiator was used to initiate polymerization of isoprene in bulk and in solution at 125 degrees C to yield PEO-b-PI block copolymers with narrow molecular weight distributions (M-w/M-n < 1.1). Polymerizations were first order in isoprene through 35% conversion. Micellar aggregates of PEO-b-PI in aqueous solution were crosslinked by treatment with a water-soluble redox initiating system, and persistent micellar structures were observed in the dry state by AFM. (c) 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 2977-2984, 2005.
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