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Keywords:

  • conjugated polymers;
  • copolymerization;
  • electrochemistry;
  • light-emitting diodes (LED);
  • polyrotaxanes;
  • supramolecular structure

Abstract

Polyfluorene PF•γCD rotaxane copolymer, composed of randomly distributed 9,9-dioctylfluorene, methyltriphenylamine (electron-donating) and 9-dicyanomethylenefluorene complexed with γ-cyclodextrin (γCD) (electron-accepting) structural units, has been synthesized by Suzuki cross-coupling reaction. The chemical structures were proved by FTIR and 1H NMR spectroscopy. The surface morphology, thermal, optical, electrochemical behavior, and adhesion characteristics of the obtained rotaxane copolymer have been investigated and compared with those of the nonrotaxane counterpart (PF). Relatively high fluorescence efficiency, almost identical normalized absorbance maximum in solution and solid-state of PF•γCD rotaxane copolymer, and a more uniform and smoother surface with lower adhesion forces provides the role of γCD encapsulation on the lower aggregation propensity. PF•γCD and PF copolymers exhibit n- and p-doping processes and blue-light emission in the film state. The optical and electrochemical band gaps (ΔEg), as well as the highest occupied molecular orbital/lowest unoccupied molecular orbital positions in an energetic diagram indicate that both copolymers are promising blue-emitting electroluminescent materials. © 2013 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013