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http://dx.doi.org/10.5012/jkcs.2007.51.3.258

Development of Highly Selective Fluorescent Chemosensors for Fluoride Ion  

Kim, Tae-Hyun (Department of Chemistry, University of Incheon)
Kim, In-Ja (Department of Chemistry, University of Incheon)
Yoo, Min-Ji (Department of Chemistry, University of Incheon)
Swager, Timothy M. (Department of Chemistry, Massachusetts Institute of Technology)
Publication Information
Journal of the Korean Chemical Society / v.51, no.3, 2007 , pp. 258-264 More about this Journal
Abstract
Novel fluoride sensory systems have been successfully developed. Previously developed method of the fluoride-induced lactonization to fluorescent molecules was detailed, and newly developed fluoride-induced aromatic cyclization scheme was introduced. Based on the strategies using the specific affinity of fluoride to silicon, our systems are highly selective for fluoride ion. Incorporation of the developed sensor to a conjugated polymer has successfully enhanced its sensitivity to fluoride ion.
Keywords
Fluoride Ion; Chemical Sensor; Fluorescence; Cyclization Reaction; Conjugated Polymer;
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1 Jung, M. E.; Lyster, M. A. J. Org. Chem. 1977, 42, 3761.   DOI
2 Jangm Y. J.; Jun, J. H.; Nakamura, K.; Koh, H. S.; Yoon, Y. J.; Yoon, J. Bull. Korean Chem. Soc. 2005, 26, 2041   DOI   ScienceOn
3 Dusemund, C.; Sandanayake, K. R. A. S.; Shinkai, S. J. Chem. Soc., Chem. Commun. 1995, 333
4 Cooper, C. R.; Spencer, N.; James, T. D. Chem. Commun. 1998, 1365
5 Nicolas, M.; Fabre, B.; Simonet, J. Chem. Commun. 1999, 1881
6 Balck, C. B.; Andrioletti, B.; Try, A. C.; Ruiperez, C.; Sessler, J. L. J. Am. Chem. Soc. 1999, 121, 10438 and references therein
7 Lehnert, W. Tetrahedron Lett. 1970, 54, 4723
8 Balck, M.; Cadogan, J. I. G. McNab, H.; MacPherson, A. D.; Rodam, V. P.; Smith, C.; Swenson, H. R. J. Chem. Soc., Perkin Trans. 1, 1997, 2483
9 Arnendola, V.; Bonizzoni, M.; Esteban-Gomez, D.; Fabbrizzi, L.; Licchelli, M.; Sancenon, F.; Taglietti, A. Coor. Chem. Rev. 2006, 250, 1451   DOI   ScienceOn
10 Kameta, N.; Hiratani, K. Chem. Lett. 2006, 35, 536.   DOI   ScienceOn
11 Mascal, M. Angew. Chem. Int. Ed. Engl. 2006, 45, 2890   DOI   ScienceOn
12 Miyaji, H.; Sato, W.; Sessler, J. L. Angew. Chem. Int. Ed. Engl. 2000, 39, 1777   DOI   ScienceOn
13 Miyaji, H.; Sessler, J. L. Angew. Chem. Int. Ed. Engl. 2001, 40, 154   DOI   ScienceOn
14 Lavigne, J. J.; Anslyn, E. V. Angew. Chem. Int. Ed. Engl. 1999, 38, 3666   DOI   ScienceOn
15 Yamaguchi, S.; Akiyama, S.; Tamao, K. J. Am. Chem. Soc. 2001, 123, 11372   DOI   ScienceOn
16 Lin, Z. H.; Ou, S. J.; Duan, C. Y.; Zhang, R. G.; Bai, Z. P. Chem. Commun. 2006, 624
17 Zhou, Q.; Swager, T. M. J. Am. Chem. Soc. 1995, 117, 12593   DOI
18 Yang, J.-S.; Swager, T. M. J. Am. Chem. Soc. 1998, 120, 5321
19 Swager, T. M. Acc. Chem. Res. 1998, 31, 210
20 McQuade, D. T.; Pullen, A. E.; Swager, T. M. Chem. Rev. 2001, 100, 2537
21 McQuade, D. T.; Hegedus, A. H.; Swager, T. M. J. Am. Chem. Soc. 2000, 122, 12389   DOI   ScienceOn
22 Swager, T. M.; Wosnick, J. H. MRS BULL. 2002, Jun. 27, 446   DOI   ScienceOn
23 Yamaguchi et al. represents a good example of demonstrating a possibility to develop a fluoride ion sensor using the affinity of silicon with fluoride ion. Yamaguchi,S.; Akiyama, S. Tamao, K. J. Am. Chem. Soc. 2000, 122, 6793   DOI   ScienceOn
24 Kim, T.-H.; Swager, T. M. Angew. Chem. Int. Ed. Engl. 2003, 42, 4803   DOI   ScienceOn
25 Drexhage, K. D. In Dye Lasers; Schafer, F. P. Ed.; Springer-Verlag: New York, U. S. A., 1977; Vol. 1