Photoluminescence and electroluminescence of methoxy and carboethoxy derivatives of 1,3-diphenyl-1H-pyrazolo[3,4-b]quinoline

Spectrochim Acta A Mol Biomol Spectrosc. 2008 Jan;69(1):22-6. doi: 10.1016/j.saa.2007.03.003. Epub 2007 Mar 13.

Abstract

A series of methoxy (MO) and carboethoxy (CE) derivatives of 1,3-diphenyl-1H-pyrazolo[3,4-b]quinoline ([DPPQ]) are characterized by spectroscopic methods. All dyes show the photoluminescent spectra which are highly solvatochromic. In the case of 6MO[DPPQ] and 6CE[DPPQ] the emission bands are broad and shifted to the red with increasing of solvent polarity whereas the dyes 6MO1pMO[DPPQ] and 6MO13pMO[DPPQ] exhibit a reverse solvatochromism. The large difference between the excited- and state-dipole moments indicates a strong electron transfer effects in all dyes. The EL spectra are obtained for the fabricated OLEDs with a general structure of EL device ITO/PVK:6X[DPPQ]/Ca/Al. The blue emission originating from PVK host matrix appears to be quenched in EL spectra of doped PVK matrix giving rise to emission in blue, blue-green or green spectral regions. The obtained results demonstrate that a series of newly synthesized methoxy and carboethoxy [DPPQ]-derivatives may be considered as promising materials for electroluminescent applications.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Electricity*
  • Luminescence*
  • Molecular Conformation
  • Pyrazoles / chemistry*
  • Quinolines / chemistry*
  • Solvents
  • Spectrum Analysis

Substances

  • 1,3-diphenyl-1H-pyrazolo(3,4-b)quinoline
  • Pyrazoles
  • Quinolines
  • Solvents
  • quinoline