Synthesis of new amphiphilic star polymers derived from a hyperbranched macroinitiator by the cationic 'grafting from' method

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • R Weberskirch - (Author)
  • R Hettich - (Author)
  • O Nuyken - (Author)
  • D Schmaljohann - (Author)
  • B. Voit - , Leibniz Institute of Polymer Research Dresden (Author)

Abstract

New amphiphilic star polymers possessing a hyperbranched core and hydrophilic graft arms have been prepared. The synthetic strategy involved esterification of the 4,4-bis(4'-hydroxyphenyl)valeric acid based hyperbranched polymer with 3-(chloromethyl)benzoyl chloride to obtain the hyperbranched macroinitiator followed by cationic ring-opening polymerization of 2-methyl-2-oxazoline to give amphiphilic polymers. Exchange of the chloride counter ion with trifluoromethanesulfonate (KCF3SO3 or AgCF3SO3) or iodide (KI) anions leads to higher polymerization rates. Phenyl 2-(chloromethyl)benzoate was used as a model initiator to study the effect of different coinitiators on the initiator efficiency. KI as a coinitiator yielded 56-86% initiator conversion whereas only 30-37% initiator conversion was achieved with KCF3SO3 or AgCF3SO3 as coinitiator after quantitative monomer consumption. Photon correlation spectroscopy (PCS) in methanol and chloroform for selected graft copolymers revealed the formation of single star molecules ranging from 22 to 50 nm in diameter.

Details

Original languageEnglish
Pages (from-to)863-873
Number of pages11
JournalMacromolecular chemistry and physics : MCP
Volume200
Issue number4
Publication statusPublished - Apr 1999
Peer-reviewedYes
Externally publishedYes

External IDs

Scopus 0001056021
ORCID /0000-0002-4531-691X/work/148607637

Keywords

Keywords

  • Ring-opening polymerization, Isomerization polymerization, Poly(ethylene oxide), Copolymers, 2-methyl-2-oxazoline, Macromolecules, 2-oxazoline, Micelles, 2-phenyl-2-oxazoline, 2-nonyl-2-oxazoline