Photochemistry of kynurenine, a tryptophan metabolite: properties of the triplet state

J Phys Chem A. 2005 Apr 28;109(16):3565-8. doi: 10.1021/jp045142k.

Abstract

Photolysis of aqueous kynurenine (KN) solutions results in the formation of triplet kynurenine TKN. In low pH solutions, triplet formation occurs with almost 100% efficiency, while in neutral solutions the triplet quantum yield is PhiT = 0.018 +/- 0.004. The dissociation constant of TKN, which is attributed to deprotonation of the anilino group, has a pKa value of 4.7. Similar triplet absorption spectra were obtained under direct and acetone-sensitized photolysis. The large difference in quantum yields as a function of pH is attributed to excited-state properties of the first excited singlet state of KN. The rate constant quenching for TKN by oxygen is kq = 2 x 10(9) M(-1) s(-1).

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Acetone
  • Animals
  • Crystallins / metabolism
  • Humans
  • Hydrogen-Ion Concentration
  • Kynurenine / chemistry*
  • Light
  • Models, Chemical
  • Photochemistry / methods*
  • Photolysis
  • Spectrophotometry
  • Spectrophotometry, Ultraviolet
  • Time Factors
  • Tryptophan / chemistry*
  • Water / chemistry

Substances

  • Crystallins
  • Water
  • Acetone
  • Kynurenine
  • Tryptophan