Synthesis and photophysical processes of an anthracene derivative containing hole transfer groups

Spectrochim Acta A Mol Biomol Spectrosc. 2011 Jan;78(1):294-7. doi: 10.1016/j.saa.2010.10.009. Epub 2010 Oct 23.

Abstract

A novel luminescent compound 9,10-di-(N-carbazovinylene)anthracene (DCVA) was synthesized by Heck reaction of 9,10-dibromoanthracene and N-vinylcarbazole. The structure was characterized by MS, 1H NMR and Elemental analysis. The photoluminescent properties of DCVA have been carefully investigated by UV-vis absorption and fluorescence emission spectra. The results showed that the luminescent quantum yield of DCVA was 0.73 in THF and it emitted blue-light with the band gap of 3.60 eV estimated from the onset absorption. In addition, the light-emission of DCVA can be quenched by electron acceptor (dimethyl terephthalate), however, the fluorescent intensities of DCVA were slowly increased with the addition of electron donor (N,N-dimethylaniline). Furthermore, the molecular interactions of DCVA with fullerene (C60) and carbon nanotubes (CNTs) were also investigated, which indicated the organic luminescent compound can be used as new fluorescent probe.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aniline Compounds / chemistry
  • Anthracenes / chemical synthesis*
  • Anthracenes / chemistry*
  • Fullerenes / chemistry
  • Luminescence
  • Nanotubes, Carbon / chemistry
  • Optical Phenomena*
  • Phthalic Acids / chemistry
  • Quantum Theory
  • Spectrometry, Fluorescence
  • Spectrophotometry, Ultraviolet

Substances

  • Aniline Compounds
  • Anthracenes
  • Fullerenes
  • Nanotubes, Carbon
  • Phthalic Acids
  • N,N-dimethylaniline
  • anthracene
  • dimethyl 4-phthalate
  • fullerene C60