Exploring reversible quenching of fluorescence from a pyrazolo[3,4-b]quinoline derivative by protonation

ChemPhysChem

Volumn 11, Issue 12, 2010, Pages 2623-2629

  Mu, Linping ^a   He, Zhiqun ^a   Kong, Xiangfei ^a   Hui, Guanbao ^a   Xu, Min ^a   Liang, Chunjun ^a   Jing, Xiping ^b   Danel, Andrzej ^c   Kulig, Ewa ^c  

^a BEIJING JIAOTONG UNIVERSITY   (China)

^b PEKING UNIVERSITY   (China)

^c University of Agriculturem   (Poland)

Author keywords

Fluorescence; Fluorescence quenching; Molecular devices; Nitrogen heterocycles; Protonation

Indexed keywords

ALKALI HALIDES; CHLORINE COMPOUNDS; FLUORESCENCE; FLUORESCENCE QUENCHING; GROUND STATE; LITHIUM COMPOUNDS; PROTONATION; RATE CONSTANTS; SODIUM HYDROXIDE; ULTRAVIOLET SPECTROSCOPY;

BIMOLECULAR ASSOCIATION; ELECTRON DISTRIBUTIONS; EQUILIBRIUM DISSOCIATION; MOLECULAR DEVICE; NITROGEN HETEROCYCLES; ORGANIC FLUORESCENT MATERIALS; QUENCHING OF FLUORESCENCE; STEADY STATE AND TRANSIENTS;

QUENCHING;

EID: 77955875328     PISSN: 14394235     EISSN: 14397641     Source Type: Journal    
DOI: 10.1002/cphc.201000152     Document Type: Article

References (51)

1. M. R. Wasielewski, W. B. Davis, W. A. Svec, M. A. Ratner, Nature 1998, 396, 60-63.
2. B. Schlicke, P. Belser, L. de Cola, E. Sabbioni, V. Balzani, J. Am. Chem. Soc. 1999, 121, 4207-4214.
3. V. Grosshenny, A. Harriman, R. Ziessel, Angew. Chem. 1995, 107, 2921-2925.
4. Angew. Chem. Int. Ed. Engl. 1995, 34, 2705-2708.
5. Molecular Switches (Ed.: B. L. Ferringa), Wiley-VCH, Weinheim, 2001.
6. M. Biancardo, C. Bignozzi, H. Doyle, G. Redmond, Chem. Commun. 2005, 3918-3920.
7. P. R. Ashton, V. Balzani, J. Becher, A. Credi, M. C. T. Fyfe, G. Mattersteig, S. Menzer, M. B. Nielsen, F. M. Raymo, J. F. Stoddart, M. Venturi, D. J. Williams, J. Am. Chem. Soc. 1999, 121, 3951-3957.
8. P. L. Boulas, M. Gómez-Kaifer, L. Echegoyen, Angew. Chem. 1998, 110, 226-258.
9. Angew. Chem. Int. Ed. 1998, 37, 216-247.
10. G. DeSantis, L. Fabbrizzi, M. Licchelli, N. Sardone, A. H. Velders, Chem. Eur. J. 1996, 2, 1243-1250.
11. R. W. Wagner, J. S. Lindsey, J. Seth, V. Palaniappan, D. F. Bocian, J. Am. Chem. Soc. 1996, 118, 3996-3997.
12. A. P. de Silva, N. H. Q. Gunaratne, C. P. McCoy, Nature 1993, 364, 42-44.
13. A. Credi, V. Balzani, S. J. Langford, J. F. Stoddart, J. Am. Chem. Soc. 1997, 119, 2679-2681.
14. T. Gunnlaugsson, D. A. Mac Dónaill, D. Parker, J. Am. Chem. Soc. 2001, 123, 12866-12876.
15. L. Chen, D. W. McBranch, H. L. Wang, R. Helgeson, F. Wudl, D. G. Whitten, Proc. Natl. Acad. Sci. USA 1999, 96, 12287-12292.
16. D. Parker, Coord. Chem. Rev. 2000, 205, 109-130.
17. Y. Kubo, S. Ishihara, M. Tsukahara, S. Tokita, J. Chem. Soc. Perkin Trans. 2 2002, 1455-1460.
18. H. A. Bassler, S. J. A. Flood, K. J. Livak, J. Marmaro, R. Knorr, C. A. Batt, Appl. Environ. Microbiol. 1995, 61, 3724-3728.
19. Y. Gabe, Y. Urano, K. Kikuchi, H. Kojima, T. Nagano, J. Am. Chem. Soc. 2004, 126, 3357-3367.
20. S. H. Lee, J. Kumar, S. K. Tripathy, Langmuir 2000, 16, 10482-10489.
21. B. A. A. Dremel, R. D. Schmid, O. S. Wolfbeis, Anal. Chim. Acta 1991, 248, 351-359.
22. L. Fabbrizzi, A. Poggi, Chem. Soc. Rev. 1995, 24, 197-202.
23. J. A. Schmidt, A. Siemiarczuk, A. C. Weedon, J. R. Bolton, J. Am. Chem. Soc. 1985, 107, 6112-6114.
24. W. M. Nau, G. Greiner, H. Rau, J. Wall, M. Olivucci, J. C. Scaiano, J. Phys. Chem. A 1999, 103, 1579-1584.
25. G. S. Beddarda, S. E. Carlina, G. Porter, Chem. Phys. Lett. 1976, 43, 27-32.
26. R. F. Chen, J. R. Knutson, Anal. Biochem. 1988, 172, 61-77.
27. Z. D. Popovic, E. R. Menzel, J. Chem. Phys. 1979, 71, 5090-5096.
28. P. B. Bisht, H. B. Tripathi, J. Lumin. 1993, 55, 153-158.
29. E. J. Bowen, W. S. Metcalf, Proc. R. Soc. Lond. A 1951, 206, 437-447.
30. T. Takahashi, K. Kikuchi, H. Kokubun, J. Photochem. 1980, 14, 67-76.
31. C. B. Murphy, Y. Zhang, T. Troxler, V. Ferry, J. J. Martin, W. E. Jones, J. Phys. Chem. B 2004, 108, 1537-1543.
32. W. R. Ware, J. Phys. Chem. 1962, 66, 455-458.
33. C. Canuel, S. Badre, H. Groenzin, M. Berheide, O. C. Mullins, Appl. Spectrosc. 2003, 57, 538-544.
34. J. R. Lakowicz, Principles of Fluorescence Spectroscopy, 3rd ed., Springer, Heidelberg, 2006, chap. 8.
35. Z. He, G. H. W. Milburn, A. Danel, A. Puchala, P. Tomasik, D. Rasala, J. Mater. Chem. 1997, 7, 2323-2325.
36. Y. T. Tao, E. Balasubramaniam, A. Danel, B. Jarosz, P. Tomasik, Appl. Phys. Lett. 2000, 77, 933-935.
37. Y. T. Tao, E. Balasubramaniam, A. Danel, B. Jarosz, P. Tomasik, Appl. Phys. Lett. 2000, 77, 1575-1577.
38. Y. T. Tao, E. Balasubramaniam, A. Danel, B. Jarosz, P. Tomasik, Chem. Mater. 2001, 13, 1207-1212.
39. L. Mu, Z. He, J. Wang, G. Hui, Y. Wang, X. Jing, A. Danel, E. Kulig, IEEE Photonics Technol. Lett. 2008, 20, 1781-1784.
40. Z. He, G. H. W. Milburn, K. J. Baldwin, D. A. Smith, A. Danel, P. Tomasik, J. Lumin. 2000, 86, 1-14.
41. Z. He, A. Danel, G. H. W. Milburn, J. Lumin. 2007, 122-123, 605-609.
42. A. R. Tamvee, Z. He, G. H. W. Milburn, A. A. Kozlov, A. V. Vannikov, A. Danel, P. Tomasik, Appl. Phys. Lett. 2000, 77, 322-324.
43. A. R. Tamvee, Z. He, G. H. W. Milburn, A. A. Kozlov, A. V. Vannikov, A. Puchala, D. Rasala, Appl. Phys. Lett. 2002, 81, 969-971.
44. A. R. Tameev, Z. He, G. H. W. Milburn, A. Danel, P. Tomasik, A. V. Vannikov, Russ. J. Electrochem. 2004, 40, 359-363.
45. J. S. de Klerk, A. N. Bader, S. Zapotoczny, M. Sterzel, M. Pilch, A. Danel, C. Gooijer, F. Ariese, J. Phys. Chem. A 2009, 113, 5273-5279.
46. M. D. Cohen, E. Fischer, J. Chem. Soc. 1962, 2, 3044-3052.
47. a values", P. M. Dewick, Essentials of Organic Chemistry: For Students of Pharmacy, Medicinal Chemistry and Biological Chemistry, Wiley, New York, 2006, Section 4.2 p. 122.
48. A. P. Kreshkov, L. N. Bykova, N. A. Kazaryan, N. Sh. Aldarova, Russ. Chem. Rev. 1962, 31, 244-266.
49. A. Yamagishi, M. Sakamoto, Bull. Chem. Soc. Jpn. 1974, 47, 2152-2157.
50. J. Niziol, A. Danel, E. Gondek, P. Armatys, J. Sanetra, G. Boiteux, Macromol. Symp. 2004, 212, 473-478.
51. E. Gondek, I. V. Kityk, A. Danel, M. Pokladko, J. Sanetra, Mater. Lett. 2007, 61, 2018-2022.