Fluorescein-based thiourea derivatives as fluorogenic sensors for mono and dicarboxylates

Sensor Letters

Volumn 8, Issue 6, 2010, Pages 818-823

  Costero, Ana M ^a,b   Parra, Margarita ^a,b   Gil, Salvador ^a,b   Colomer, Josep Vicent ^a,b   Martí, Almudena ^a,b  

^a UNIVERSITAT POLITÈCNICA DE VALÈNCIA   (Spain)

^b UNIVERSITY OF VALENCIA   (Spain)

Author keywords

Aggregation; Carboxylate sensing; Fluorescence; Molecular recognition; Thioureas

Indexed keywords

AGGREGATION; ANION SENSING; CARBOXYLATE SENSING; DICARBOXYLATES; FLUOROGENICS; MALEATE; PHOTOPHYSICAL PROPERTIES; SIGNALING UNITS; TARGET MOLECULE; THIOUREA DERIVATIVES;

CARBOXYLATION; CHELATION; FLUORESCENCE; LIGANDS; MOLECULAR BIOLOGY; MOLECULAR RECOGNITION; NEGATIVE IONS; THIOUREAS;

UREA;

EID: 79955425950     PISSN: 1546198X     EISSN: None     Source Type: Journal    
DOI: 10.1166/sl.2010.1351     Document Type: Article

References (28)

1. M. Goncalves and T. Sameiro, Chem. Rev. 109, 190 (2009).
2. O. Minet, J. Beuthan, V. Mildaziene, and R. Baniene, Rev. Fluor. 1, 195 (2004).
3. M. K. Johansson and R. M. Cook, Chem.-Eur. J. 9, 3466 (2003).
4. T. Matsuya, N. Hoshino, and T. Okuyama, Curr. Anal. Chem. 2, 397 (2006).
5. P. Scully, R. Chandy, R. Edwards, D. Merchant, and R. Morgan, Environ. Sci. Res. 56, 175 (2001).
6. S. Royo, R. Martínez-Máñez, F. Sancenón, A. M. Costero, M. Parra, and S. Gil, Chem. Commun. 48390 (2007).
7. B. C. Giordano and G. E. Collins, Curr. Org. Chem. 11, 255 (2007).
8. M. Burnworth, S. J. Rowan, and C. Werder, Chem.-Eur. J. 13, 7828 (2007).
9. X.-F. Yang, L. Wang, H. Xu, and M. Zhao, Anal. Chim. Acta 631, 91 (2009).
10. J.-S. Wu, H. J. Kim, M. H. Lee, J. H. Yoon, J. H. Lee, and J. S. Kim, Tetrahedron Lett. 48, 3159 (2007).
11. X. Zhang, Y. Shiraishi, and T. Hirai, Tetrahedron Lett. 48, 8803 (2007).
12. C. Caltagirone and P. A. Gale, Chem. Soc. Rev. 38, 520 (2009).
13. Z.-h. Lin, L.-x. Xie, Y.-g. Zhao, C.-y. Duan, and J.-p. Qu, Org. Biomol. Chem. 5, 3535 (2007).
14. K. Rang, J. Sandström, and C. Svensson, Can. J. Chem. 76, 811 (1998).
15. D. A. Jose, D. K. Kumar, P. Kar, S. Verma, A. Ghosh, B. Ganguly, H. N. Ghosh, and A. Das, Tetrahedron 63, 12007 (2007).
16. F. Sansone, E. Chierici, A. Casnati, and R. Ungaro, Org. Biomol. Chem. 1, 1802 (2003).
17. A. M. Costero, P. Gaviña, G. M. Rodríguez-Muñiz, and S. Gil, Tetrahedron 63, 7899 (2007).
18. K.-J. Kim, J.-M. Lee, and S.-K. Ryu, Sep. Technol. 6, 211 (1996).
19. A. Mosunov and J. J. Dannenberg, J. Phys. Chem. B 104, 806 (2000).
20. A. M. Costero, M. Colera, P. Gaviña, S. Gil, M. Kubinyi, K. Pál, and M. Kállay, Tetrahedron 64, 3217 (2008).
21. A. M. Costero, M. Colera, P. Gaviña, and S. Gil, Chem. Commun. 761 (2006).
22. H. N. Kim, M. H. Lee, H. J. Kim, J. S. Kim, and J. Yoon, Chem. Soc. Rev. 37, 1465 (2008).
23. R. Custelcean, Chem. Commun. 295 (2008).
24. M. Nickoleit, A. Uhl, and J. Bendig, Laser Chem. 17, 161 (1977).
25. R. Sjöback, J. Nygren, and M. Kubista, Spectrochim. Acta, Part A 51, L7 (1995).
26. C. Lee, Y. W. Sung, and J. W. Park, J. Phys. Chem. B 103, 893 (1999).
27. SPECFIT/32 Global Analysis System v. 3.0, Spectrum Associates (Marlborough, MA, USA), www.bio-logic.info/rapid-kinetics/specfit.html.
28. J. E. Barry, M. Finkelstein, and S. D. Ross, J. Org. Chem. 41, 64 (1982).