Characterisation of the lowest singlet and triplet excited states of S-flurbiprofen

Photochem Photobiol Sci. 2004 Nov-Dec;3(11-12):1038-41. doi: 10.1039/b408530b. Epub 2004 Nov 8.

Abstract

The photophysical properties of S-flurbiprofen [S-2-fluoro-alpha-methyl-4-biphenylacetic acid], a nonsteroidal anti-inflammatory drug, have been examined using steady-state and time-resolved spectroscopic techniques. The energy of its first singlet excited state is 99 kcal mol(-1). The fluorescence quantum yields and lifetimes (at 300 nm) have been determined in acetonitrile, methanol, hexane and PBS; they are in the range 0.15<phi(F)< 0.33 and 0.7<tau(F)<2.0 ns. The intersystem crossing quantum yields are between 0.45 and 0.71; the lambda(max) of the T-T absorption is 360 nm, and the triplets live from 15 to 106 micros. Steady state photolysis in aqueous medium leads to S-2-hydroxy-alpha-methyl-4-biphenylacetic acid via photonucleophilic aromatic substitution, in addition to the photodecarboxylation products observed in organic solvents.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Inflammatory Agents, Non-Steroidal / chemistry*
  • Benzophenones
  • Chromatography, High Pressure Liquid
  • Flurbiprofen / chemistry*
  • Lasers
  • Magnetic Resonance Spectroscopy
  • Photolysis
  • Solvents
  • Spectrometry, Fluorescence

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Benzophenones
  • Solvents
  • Flurbiprofen
  • benzophenone