• DocumentCode
    3488974
  • Title

    Synthesis and optical properties of azo-substituted polythiophene

  • Author

    Goncalves, V.C. ; Balogh, D.T.

  • Author_Institution
    Inst. de Fisica de Sao Carlos, Sao Paulo Univ., Sao Carlos, Brazil
  • fYear
    2005
  • fDate
    11-14 Sept. 2005
  • Firstpage
    518
  • Lastpage
    519
  • Abstract
    The polythiophenes have been widely used as a conducting polymer and in many others applications such as electrochromism. The introduction of an azobenzene group can extend the possible applications to other fields, such as optical memories. In this work, a thiophenic monomer with an azobenzene moiety at the 3-position of the thiophene ring was synthesized by esterification reaction between the commercial dye disperse red 1 (DR1) and 3-thiopheneacetic acid. The UV-Vis spectra of polymer in solution were obtained and used to study the possible solvato- and thermochromic properties of the polymer. The thermochromic property was analyzed in the temperature interval of 10 to 70 °C. The solvents used in the solvatochromic study were hexane, chloroform, tetrahydrofuran, toluene, acetone, methanol, acetonitrile and dimethylformamide.
  • Keywords
    conducting polymers; dyes; electrochromism; materials preparation; thermo-optical effects; ultraviolet spectra; visible spectra; 10 to 70 C; 3-thiopheneacetic acid; UV spectra; acetone; acetonitrile; azo-substituted polythiophene; azobenzene group; chloroform; commercial dye disperse red 1; conducting polymer; dimethylformamide; electrochromism; esterification reaction; hexane; methanol; optical memories; optical properties; solvatochromic study; tetrahydrofuran; thermochromic properties; toluene; visible spectra; Chemicals; Electrochromism; Methanol; Nonlinear optics; Optical polymers; Optical sensors; Purification; Solvents; Temperature; Thermochromism;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Electrets, 2005. ISE-12. 2005 12th International Symposium on
  • Print_ISBN
    0-7803-9116-0
  • Type

    conf

  • DOI
    10.1109/ISE.2005.1612440
  • Filename
    1612440