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Keywords:

  • carbon nanotubes;
  • poly(ε-caprolactone);
  • ring opening polymerization;
  • click chemistry

Abstract

Multi-walled carbon nanotubes (MWNTs) were covalently functionalized with poly(ε-caprolactone) (PCL) using click chemistry. First, chlorine moiety-containing PCL was synthesized by the copolymerization of α-chloro-ε-caprolactone with ε-caprolactone monomer using ring opening polymerization, and further converted to azide moiety-containing PCL. The alkyne-functionalized MWNTs were prepared with the treatment of p-amino propargyl ether using a solvent free diazotization procedure. The covalent functionalization of alkyne-derived MWNTs with azide moiety-containing PCL was accomplished using Cu(I)-catalyzed [3+2] Huisgen dipolar cycloaddition click chemistry. The PCL-functionalization of MWNTs was confirmed by the measurements of Fourier transform infra-red, NMR, Raman spectroscopy, scanning electron microscopy, and transmission electron microscopy. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011