Calix[4]crown in dual sensing functions with FRET

Tetrahedron Letters

Volumn 46, Issue 47, 2005, Pages 8163-8167

  Lee, Seoung Ho ^a   Sung, Kuk Kim ^a   Ju, Han Bok ^a   Suh, Hyun Lee ^a   Yoon, Juyoung ^b   Lee, Kilsung ^c   Jong, Seung Kim ^a  

^a Dankook University   (South Korea)

^b Ewha Womans University   (South Korea)

^c Cheil Industries Inc   (South Korea)

Author keywords

Calixarenes; Fluorescence; Metal ion complexation

Indexed keywords

CALIXARENE; LEAD; METAL ION;

ARTICLE; FLUORESCENCE RESONANCE ENERGY TRANSFER; MOLECULAR PROBE; ULTRAVIOLET RADIATION;

EID: 27144496642     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2005.09.117     Document Type: Article

References (36)

1. J.P. Desvergne A.W. Czarnik Chemosensors of Ion and Molecule Recognition NATO ASI series 1997 Kluwer Academic Dordrecht
2. A.P. de Silva, H.Q. Gunaratne, N.T.A. Gunnlaugsson, T.M. Huxley, C.P. McCoy, J.T. Rademacher, and T.E. Rice Chem. Rev. 97 1997 1515
3. L. Prodi, M. Montalti, N. Zaccheroni, J.S. Bradshaw, R.M. Izatt, and P.B. Savage Tetrahedron Lett. 42 2001 2941
4. K. Rurack, M. Kollmannsberger, U. Resch-Genger, and J. Daub J. Am. Chem. Soc. 122 2000 968
5. D.W. Brousmiche, J.M. Serin, J.M.J. Fréchet, G.S. He, T. Lin, S.J. Chung, and P.N. Prasad J. Am. Chem. Soc. 125 2003 1448
6. X. Tang, and I.J. Dmochowski Org. Lett. 7 2005 279
7. A. Ono, and H. Togashi Angew. Chem., Int. Ed. 43 2004 4300
8. N.J. van der Veen, S. Flink, M.A. Deij, R.J.M. Egberink, F.C.J.M. van Veggel, and D.N. Reinhoudt J. Am. Chem. Soc. 122 2000 6112
9. P.D. Beer Acc. Chem. Res. 31 1998 71
10. H.-F. Ji, G.M. Brown, and R. Dabestani Chem. Commun. 1999 609
11. H.-F. Ji, R. Dabestani, G.M. Brown, and R.A. Sachleben Chem. Commun. 2000 833
12. H.-F. Ji, R. Dabestani, G.M. Brown, and R.L. Hettich J. Chem. Soc., Perkins Trans. 2 2001 585
13. C.D. Gutsche J.F. Stoddart Calixarenes, Monographs in Supramolecular Chemistry Vol. 1 1989 Royal Society of Chemistry Cambridge UK
14. J. Vicens V. Böhmer Calixarenes: A Versatile Class of Macrocyclic Compounds 1991 Kluwer Dordrecht
15. V. Böhmer Angew. Chem., Int. Ed. 34 1995 713
16. J.S. Kim, O.J. Shon, J.W. Ko, M.H. Cho, I.Y. Yu, and J. Vicens J. Org. Chem. 65 2000 2386
17. J.S. Kim, W.K. Lee, K. No, Z. Asfari, and J. Vicens Tetrahedron Lett. 41 2000 3345
18. I. Aoki, T. Sakaki, and S. Shinkai J. Chem. Soc., Chem. Commun. 1992 730
19. T. Jin, K. Ichikawa, and T. Koyama J. Chem. Soc., Chem. Commun. 1992 499
20. R. Métivier, I. Leray, and B. Valeur J. Chem. Soc., Chem. Commun. 2003 996
21. R. Métivier, I. Leray, and B. Valeur Chem. Eur. J. 10 2004 4480
22. I. Leray, F. O'Reilly, J.-L. Habib Jiwan, J.-Ph. Soumillion, and B. Valeur Chem. Commun. 1999 795
23. H.-F. Ji, R. Dabestani, and G.M. Brown J. Am. Chem. Soc. 122 2000 9306
24. J.S. Kim, O.J. Shon, J.A. Rim, S.K. Kim, and J. Yoon J. Org. Chem. 67 2002 2348
25. J.S. Kim, K.H. Noh, S.H. Lee, S.K. Kim, S.K. Kim, and J. Yoon J. Org. Chem. 68 2003 597
26. S.K. Kim, S.H. Lee, J.Y. Lee, R.A. Bartsch, and J.S. Kim J. Am. Chem. Soc. 126 2004 16499
27. J.Y. Lee, S.K. Kim, J.H. Jung, and J.S. Kim J. Org. Chem. 70 2005 1463
28. J.Y. Kim, G.C. Kim, C.R. Kim, S.H. Lee, J.H. Lee, and J.S. Kim J. Org. Chem. 68 2003 1933
29. S.H. Lee, J.Y. Kim, J. Ko, J.Y. Lee, and J.S. Kim J. Org. Chem. 69 2004 2902
30. S.H. Lee, J.Y. Kim, S.K. Kim, J.H. Lee, and J.S. Kim Tetrahedron 60 2004 5171
31. J.R. Lakowicz Principles of Fluorescence Spectroscopy 2nd ed. 1999 Plenum New York
32. 3: C, 59.26; H, 3.73. Found: C, 59.21; H, 3.74.
33. 3CN). For all fluorescence measurements, the excitation was made at 344 nm to give fluorescence intensity at room temperature.
34. J.S. Kim, O.J. Shon, J.K. Lee, S.H. Lee, J.Y. Kim, K.M. Park, and S.S. Lee J. Org. Chem. 67 2002 1372
35. Association constants were obtained using the computer program enzfitter, available from Elsevier-BIOSOFT, 68 Hills Road, Cambridge CB2 1LA, United Kingdom.
36. K.A. Connors Binding Constants 1987 New York Wiley