4.5 Article

Self-Assembly of Block Copolymer Micelles: Synthesis via Reversible Addition-Fragmentation Chain Transfer Polymerization and Aqueous Solution Properties

Journal

JOURNAL OF PHYSICAL CHEMISTRY B
Volume 114, Issue 28, Pages 9128-9134

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jp102919t

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Funding

  1. Institute of Materials Research and Engineering (IMRE)
  2. Agency for Science, Technology and Research (A*STAR)

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Poly(hexafluorobutyl methacrylate) (PHFBMA) homopolymer was synthesized by reversible addition fragmentation chain transfer (RAFT)-mediated living radical polymerization in the presence of cyano-2-propyl dithiobenzoate (CPDB) RAFT agent. A block copolymer of PHFBMA-poly(propylene glycol acrylate) (PHFBMA-b-PPGA) with dangling poly(propylene glycol) (PPG) side chains was then synthesized by using CPDB-terminated PHFBMA as a macro-RAFT agent. The amphiphilic properties and self-assembly of PHFBMA-b-PPGA block copolymer in aqueous solution were investigated by dynamic and static light scattering (DLS and SLS) studies, in combination with fluorescence spectroscopy and transmission electron microscopy (TEM). Although PPG shows moderately hydrophilic character, the formation of nanosize polymeric micelles was confirmed by fluorescence and TEM studies. The low value of the critical aggregation concentration exhibited that the tendency for the formation of copolymer aggregates in aqueous solution was very high due to the strong hydrophobicity of the PHFBMA(145)-b-PPGA(33) block copolymer. The combination of DLS and SLS measurements revealed the existence of micellar aggregates in aqueous solution with an association number of similar to 40 +/- 7 for block copolymer micelles. It was also found in TEM observation that there are 40-50 micelles accumulated into one aggregate and these micelles are loosely packed inside the aggregate.

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