A cyclam-type "turn on" fluorescent sensor selective for mercury ions in aqueous media

RSC Advances

Volumn 2, Issue 33, 2012, Pages 12679-12682

  Voutsadaki, Styliani ^a   Tsikalas, George K ^a   Klontzas, Emmanuel ^a   Froudakis, George E ^a   Pergantis, Spiros A ^a   Demadis, Konstantinos D ^a   Katerinopoulos, Haralambos E ^a  

^a UNIVERSITY OF CRETE   (Greece)

Author keywords

[No Author keywords available]

Indexed keywords

AQUEOUS MEDIA; FLUORESCENT SENSORS; ION PROBE; ION SELECTIVITY; MERCURY ION; SPECTRAL PROFILE;

FLUORESCENCE; FUNCTIONAL GROUPS; MERCURY (METAL); PROBES; SENSORS;

IONS;

EID: 84870003230     PISSN: None     EISSN: 20462069     Source Type: Journal    
DOI: 10.1039/c2ra20971c     Document Type: Article

References (39)

1. E. M. Nolan S. J. Lippard Chem. Rev. 2008 108 3443
2. I. W. Zhu Y. Xu X. Qian Prog. Chem. 2007 19 1229
3. Leray B. Valeur Eur. J. Inorg. Chem. 2009 3525
4. D. W. Domaille E. L. Que C. J. Chang Nat. Chem. Biol. 2008 4 168
5. Y.-W. Lin C.-C. Huang H.-T. Chang Analyst 2011 136 863
6. X. Qian Y. Xiao Y. Xu X. Guo J. Qian W. Zhu Chem. Commun. 2010 46 6418
7. N. Kaur S. Kumar Tetrahedron 2011 67 9233
8. M. Dutta D. Das Trends Anal. Chem. 2012 32 113
9. H. N. Kim W. X. Ren J. S. Kim J. Yoon Chem. Soc. Rev. 2012 41 3210
10. S. Voutsadaki G. K. Tsikalas E. Klontzas G. E. Froudakis H. E. Katerinopoulos Chem. Commun. 2010 46 3292
11. R. L. Deming A. L. Allred A. R. Dahl A. W. Herlinger M. O. Kestner J. Am. Chem. Soc. 1976 98 4132 4137
12. K.-C. Song M. H. Kim H. J. Kim S.-K. Chang Tetrahedron Lett. 2007 48 7464
13. M. P. Sang H. K. Mi J.-I. Choe S.-K. Chang J. Org. Chem. 2007 72 3550
14. S.-Y. Moon J. Y. Na M. P. Sang S.-K. Chang J. Org. Chem. 2005 70 2394
15. N. J. Youn S.-K. Chang Tetrahedron Lett. 2005 46 125
16. J. Kotek and P. Hermann, Ten-membered Rings or Larger with One or More Nitrogen Atoms, in Comprehensive Heterocyclic Chemistry III, ed., A. R. Katritzky, C. A. Ramsden, E. F. V. Scriven, and, R. J. K. Taylor, Elsevier, Oxford, 2008, vol. 14, pp. 613-666
17. W. Yang C. M. Giandomenico M. Sartori D. A. Moore Tetrahedron Lett. 2003 44 2481
18. F. Weygand W. Swodenk Chem. Ber. 1957 90 639
19. F. Weygand E. Frauendorfer Chem. Ber. 1970 103 2437
20. J. A. Halfen V. G. Young, Jr. Chem. Commun. 2003 2894
21. R. J. Bergeron J. S. McManis J. Org. Chem. 1988 53 3108
22. C. Li W.-T. Wong Tetrahedron 2004 60 5595
23. T. G. Greene and P. G. M. Wuts, Protective Groups in Organic Synthesis, Wiley-Interscience, New York, 2nd edn, 1991, pp. 353-354
24. W. H. Melhuish J. Phys. Chem. 1961 65 229
25. G. Grynkiewicz M. Poenie R. Y. Tsien J. Biol. Chem. 1985 260 3350
26. K. F. Sibbons M. Al-Hashimi M. Motevalli J. Wolowska M. Watkinson Dalton Trans. 2004 3163
27. C. Schickaneder F. W. Heinemann R. Alsfasser Eur. J. Inorg. Chem. 2006 2357
28. K. M. Dean Y. Qin A. E. Palmer Biochim. Biophys. Acta, Mol. Cell Res. 2012 1823 1406
29. J. J. Stewart J. Mol. Model. 2007 13 1173
30. J. J. Stewart J. Mol. Model. 2008 14 499 535
31. J. J. P. Stewart MOPAC2009
32. J. J. P. Stewart Stewart Computational Chemistry
33. F. Weigend M. Haser H. Patzelt R. Ahlrichs Chem. Phys. Lett. 1998 294 143
34. A. D. Becke Phys. Rev. A 1988 38 3098
35. J. P. Perdew Phys. Rev. B 1986 33 8822
36. F. Weigend R. Ahlrichs Phys. Chem. Chem. Phys. 2005 7 3297
37. A. Schäfer H. Horn R. Ahlrichs J. Chem. Phys. 1992 97 2571
38. R. Ahlrichs M. Bär M. Häser H. Horn C. Kölmel Chem. Phys. Lett. 1989 162 165
39. A. Klamt G. Schuurmann J. Chem. Soc., Perkin Trans. 2 1993 799 805