DOI QR코드

DOI QR Code

Photophysical Properties of Khellin-Dimethylfumarate C$_4$-Cyclomonoadduct

  • Shim, Sang-Chul (Department of Chemistry, Korea Advanced Institute of Science and Technology) ;
  • Kang, Ho-Kwon (Department of Chemistry, Korea Advanced Institute of Science and Technology)
  • 발행 : 1986.12.20

초록

The fluorescence intensity of khellin-dimethylfumarate C$_4$-cycloadduct (KDF) is very sensitive to temperature and to the nature of solvents, especially hydrogen-bonding ability. The fluorescence quantum yields of KDF in ethanol and isopentane at 77K are 0.73 and 0.54, respectively, both of which are much larger than the room temperature values. The phosphorescence lifetime is very long and decreases with decreasing the solvent polarity. The phosphorescence and fluorescence quantum yield ratio is very small and decreases with decreasing solvent polarity. The solvent relaxation plays an important role in the excited states of KDF. The internal conversion is a major decay process of the excited singlet state of KDF in all the solvents used at room temperature.

키워드

참고문헌

  1. J. Am. Chem. Soc. v.72 A. Schonberg;A. Sina
  2. Biochim. Biophys. Acta v.475 E. Cassuto;N. Gross;E. Bardwell;P. Howard-Flanders
  3. Dermatologica v.165 A. Abdel-Fatta;M.N. Aboul-Enein;G.M. Wassel;B.S. El-Menshawi
  4. Photochem. Photobiol. v.39 B. Ortel;A. tanew;K. Wolff;H. Honigsmann
  5. Photochem. Photobiol. v.38 B.F. Abeysekera;Z. Abramowski;G.H.N. Towers
  6. J. Am. Chem. Soc. v.95 W.W. Mantulin;P.-S. Song
  7. Photochem. Photobiol. v.32 B.J. Parson
  8. Biochemistry v.21 D. Kanne;K. Straub;H. Rapoport;J.E. Hearst
  9. J. Am. Chem. Soc. v.104 D. Kanne;K. Straub;J.E. Hearst;H. Rapoport
  10. J. Chem. Phys. v.37 T. Azumi;S.P. McGlynn
  11. Photoluminescence of Solutions C.A. Parker;C.A. Parker(ed.)
  12. Analyst v.87 C.A. Parker;C.G. Hatchard
  13. J. Chem. Phys. v.68 W.A. Wassam Jr.;E.C. Lim
  14. J. Chem. Phys. v.69 W.A. Wassam;E.C. Lim
  15. J. Chem. Phys. v.65 S.L. Madej;S. Okajima;E.C. Lim
  16. J. Am. Chem. Soc. v.104 T.-I. Lai;B.T. Lim;E.C. Lim
  17. J. Am. Chem. Soc. v.107 T.-I. Lai;E.C. Lim
  18. J. Am. Chem. Soc. v.86 W.G. Herkstroeter;A.A. Lamola;G.S. Hammond
  19. J. Am. Chem. Soc. v.91 J. W. Hanifin;E. Cohen