Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
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Pyrene-coumarin Based Calix Fluorophore Emitting Exciplex

  • Lee, Yeon-Ok (Department of Chemistry, Institute of Nanosensor & Biotechnology, Dankook University) ;
  • Lee, Ji-Yeon (Department of Chemistry, Institute of Nanosensor & Biotechnology, Dankook University) ;
  • Quang, Duong Tuan (Department of Chemistry, Institute of Nanosensor & Biotechnology, Dankook University) ;
  • Lee, Min-Hee (Department of Chemistry, Institute of Nanosensor & Biotechnology, Dankook University) ;
  • Kim, Jong-Seung (Department of Chemistry, Institute of Nanosensor & Biotechnology, Dankook University)
  • Published : 2006.09.20
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References

  1. Lioyd, S. Nature 2000, 406, 1047 https://doi.org/10.1038/35023282
  2. Voss, D. Nature 2000, 407, 442 https://doi.org/10.1038/35035212
  3. Ball, P. Nature 2000, 406, 118 https://doi.org/10.1038/35018259
  4. Schliche, B.; Belser, P.; De Cola, L.; Sabbioni, E.; Balzani, V. J. Am. Chem. Soc. 1999, 121, 4207 https://doi.org/10.1021/ja990044b
  5. Cygan, M. T.; Dunbar, T. D.; Arnold, J. J.; Bumn, L. A.; Shedlock, N. F.; Burgin, T. P.; Jones, L. II; Allara, D. L.; Tour, J. M.; Weiss, P. S. J. Am. Chem. Soc. 1998, 120, 2721 https://doi.org/10.1021/ja973448h
  6. Gutsche, C. D. Calixarenes; Royal Society of Chemistry: Cambridge, 1989
  7. Gutsche, C. D. In Synthesis of Macrocycles: Design of Selective Complexing Agents; Izatt, R. M., Christensen, J. J., Eds.; Wiley: New York, 1987; p 93
  8. Calixarenes: A Versatile Class of Macrocyclic Compounds; Vicens, J.; Bohmer, V., Eds.; Kluwer: Dordrecht, 1991
  9. Bohmer, V.; McKervey, M. A. Chem. Zeit 1991, 195
  10. Gutsche, C. D. In Calixarenes, Monographs in Supramolecular Chemistry; Stoddart, J. F., Ed.; Royal Society of Chemistry: Cambridge, U. K., 1989; Vol. 1. 9
  11. Lee, J. K.; Sim, W.; Kim, S. K.; Bok, J. H.; Lim, M. S.; Lee, S. W.; Cho, N. S.; Kim,, J. S. Bull. Korean Chem. Soc. 2004, 25, 314 https://doi.org/10.5012/bkcs.2004.25.2.314
  12. Kim, S. K.; Lee, J. K.; Lim, J. M.; Kim, J. W.; Kim, J. S. Bull. Korean Chem. Soc. 2004, 25, 1247 https://doi.org/10.5012/bkcs.2004.25.8.1247
  13. Andreetti, G. D.; Ugozzoli, F.; Ungaro, R.; Pochini, A. In Inclusion Compounds; Atwood, J. L., Davies, J. E. D., MacNicol, D. D., Eds.; Oxford University Press: New York, 1991; Vol. 4, pp 64-125
  14. Aoki, L.; Sakaki, T.; Shinkai, S. J. Chem. Soc., Chem. Commun. 1992, 730
  15. Jin, T.; Ichikawa, K.; Koyama, T. J. Chem. Soc., Chem. Commun. 1992, 499
  16. Ji, H.-F.; Brown, G. M.; Dabestani, R. Chem. Commun. 1999, 609
  17. Kim, J. S.; Shon, O. J.; Rim, J. A.; Kim, S. K.; Yoon, J. J. Org. Chem. 2002, 67, 2348 https://doi.org/10.1021/jo010877w
  18. Kim, J. S.; Noh, K. H.; Lee, S. H.; Kim, S. K.; Kim, S. K.; Yoon, J. J. Org. Chem. 2003, 68, 597 https://doi.org/10.1021/jo020538i
  19. Leray, I.; Lefevre, J.-P.; Delouis, J.-F.; Delaire, J.; Valeur, B. Chem. Eur. J. 2001, 7(21), 4590 https://doi.org/10.1002/1521-3765(20011105)7:21<4590::AID-CHEM4590>3.0.CO;2-A
  20. Hecht, S.; Vladimirov, N.; Frechet, J. M. J. J. Am. Chem. Soc. 2001, 123, 18 https://doi.org/10.1021/ja003304u
  21. Mizukami, S.; Nagano, T.; Urano, Y.; Odani, A.; Kikuchi, K. J. Am. Chem. Soc. 2002, 124, 3920 https://doi.org/10.1021/ja0175643
  22. van der Veen, N.; Flink, S.; Deij, M. A.; Egberink, R. J. M.; van Veggel, F. C. J. M.; Reinhoudt, D. N. J. Am. Chem. Soc. 2000, 122, 6112 https://doi.org/10.1021/ja000713h
  23. Birks, J. B. Photophysics of Aromatic Molecules; Wiley-Interscience: London, 1970
  24. Koh, K. N.; Araki, K.; Shinkai, S.; Asfari, Z.; Vicens, J. Tetrahedron Lett. 1995, 36, 6095 https://doi.org/10.1016/0040-4039(95)01212-Z
  25. Lee, S. H.; Kim, S. H.; Kim, S. K.; Jung, J. H.; Kim, J. S. J. Org. Chem. 2005, 70, 9288 https://doi.org/10.1021/jo051302s
  26. No, K.; Lee, H. J.; Park, K. M.; Lee, S. S.; Noh, K. H.; Kim, S. K.; Lee, J. Y.; Kim, J. S. J. Heterocyclic Chem. 2004, 41, 211 https://doi.org/10.1002/jhet.5570410211
  27. Lee, J. Y.; Kim. S. K.; Jung, J. H.; Kim, J. S. J. Org. Chem. 2005, 70, 1463 https://doi.org/10.1021/jo048228i
  28. Fossum, R. D.; Fox, M. A. J. Phys. Chem. B 1997, 101, 6384 https://doi.org/10.1021/jp9704123
  29. Hossain, M. A.; Mihara, H.; Ueno, A. S. J. Am. Chem. Soc. 2003, 125, 11178 https://doi.org/10.1021/ja036427y
  30. Seth, D.; Chakraborty, A.; Setua, P.; Chakrabarty, D.; Sekar, N. J. Phys. Chem. B 2005, 109, 1208

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