• DocumentCode
    3004851
  • Title

    Synthesis and Properties of Photochromic Diarylethene Derivatives Bearing Benzofuran and Isoxazole Units

  • Author

    Li, Xiaoting ; Liu, Weijun ; Pu, Shouzhi ; Li, Hui

  • Author_Institution
    Jiangxi Key Lab. of Org. Chem., Jiangxi Sci. & Technol. Normal Univ., Nanchang, China
  • fYear
    2012
  • fDate
    21-23 May 2012
  • Firstpage
    1
  • Lastpage
    4
  • Abstract
    A new unsymmetrical photochromic diarylethene, 1(2-ethyl-3-benzofuranyl)-2(3,5-dimethyl-4-isoxazolyl) perfluorocyclopentene(1a)were synthesized, and its properties, such as photochromism and fluorescence properties in solution as well as in poly-methylmethacrylate (PMMA) amorphous films, were investigated in detail. The results showed that this compound had good thermal stability and exhibited reversible photochromism, changing from colorless to yellow after irradiation with UV light both in solution and in PMMA amorphous film. The open-ring isomer of the diarylethene 1a exhibited relatively strong fluorescence at 401 nm in hexane solution (2 × 10-5 mol/L) when excited at 307 nm and 408 nm in PMMA amorphous film when excited at 282 nm. The fluorescence intensity decreased along with the photochromism upon irradiation with 297 nm light.
  • Keywords
    fluorescence; liquid phase deposition; photochromism; polymer films; thermal stability; ultraviolet radiation effects; 1(2-ethyl-3-benzofuranyl)-2(3,5-dimethyl-4-isoxazolyl) perfluorocyclopentene; UV light irradiation; benzofuran units; fluorescence properties; isoxazole units; open-ring isomer; photochromic diarylethene derivatives; photochromism; poly-methylmethacrylate amorphous films; thermal stability; wavelength 282 nm; wavelength 307 nm; Absorption; Chemistry; Compounds; Films; Fluorescence; Photochromism; Radiation effects;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Photonics and Optoelectronics (SOPO), 2012 Symposium on
  • Conference_Location
    Shanghai
  • ISSN
    2156-8464
  • Print_ISBN
    978-1-4577-0909-8
  • Type

    conf

  • DOI
    10.1109/SOPO.2012.6271041
  • Filename
    6271041