Abstract
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 ≈ 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 °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.
| Original language | English |
|---|---|
| Pages (from-to) | 2977-2984 |
| Number of pages | 8 |
| Journal | Journal of Polymer Science, Part A: Polymer Chemistry |
| Volume | 43 |
| Issue number | 14 |
| DOIs | |
| State | Published - Jul 15 2005 |
Keywords
- Amphiphiles
- Diblock copolymers
- Micelles
- Nitroxide-mediated polymer-ization
Fingerprint
Dive into the research topics of 'Preparation of poly(ethylene oxide)-block-poly(isoprene) by nitroxide-mediated free radical polymerization from PEO macroinitiators'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver