A sensitive and selective "turn on" fluorescent chemosensor for Hg(II) ion based on a new pyrene-thymine dyad

Analytica Chimica Acta

Volumn 549, Issue 1-2, 2005, Pages 10-13

  Wang, Zhuo ^a,b   Zhang, Deqing ^a   Zhu, Daoben ^a  

^a INSTITUTE OF CHEMISTRY   (China)

^b UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

Author keywords

Chemosensor; Excimer emission; Fluorescence; Hg(II) ion; Pyrene; Thymine

Indexed keywords

FLUORESCENCE; MERCURY (METAL); SYNTHESIS (CHEMICAL);

EXCIMER EMISSIONS; FLUORESCENT CHEMOSENSORS; HG (II) IONS; METAL IONS; PYRENE; THYMINE;

CHEMICAL SENSORS;

MERCURY; PYRENE; THYMINE;

ANALYTIC METHOD; ARTICLE; CHEMICAL STRUCTURE; CHEMOSENSITIVITY; FLUORESCENCE ANALYSIS; PHOTOCHEMICAL QUENCHING; PRIORITY JOURNAL; SPECTROFLUOROMETRY; STRUCTURE ANALYSIS; SYNTHESIS;

EID: 23844435354     PISSN: 00032670     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.aca.2005.06.031     Document Type: Article

References (27)

1. G.E. McKeown-Eyssen, J. Ruedy, and A. Neims Am. J. Epidemiol. 118 1983 470
2. P.W. Davidson, G.J. Myers, C. Cox, C.F. Shamlaye, D.O. Marsh, M.A. Tanner, M. Berlin, J. Sloane-Reeves, E. Cernichiari, O. Choisy, A. Choi, and T.W. Clarkson Neurotoxicology 16 1995 677
3. P. Grandjean, P. Heihe, R.F. White, and F. Debes Environ. Res. 77 1998 165
4. T. Takeuchi, N. Morikawa, H. Matsumoto, and Y. Shiraishi Acta Neuropathol. 2 1962 40
5. H. Matsumoto, G. Koya, and T. Takeuchi J. Neuropathol. Exp. Neurol. 24 1965 563
6. M. Harada Crit. Rev. Toxicol. 25 1995 1
7. M.Y. Chea, and A.W. Czarnik J. Am. Chem. Soc. 114 1992 9704
8. G. Zhang, D. Zhang, S. Yin, X. Yang, Z. Shuai, and D. Zhu Chem. Commun. 2005 2161
9. J. Yoon, N.E. Ohler, D.H. Vance, W.D. Aumiller, and A.W. Czarnik Tetrahedron Lett. 38 1997 3845
10. D.Y. Sasaki, and B.E. Padilla Chem. Commun. 1998 1581
11. X.-B. Zhang, C.-C. Guo, Z.-Z. Li, G.-L. Shen, and R.-Q. Yu Anal. Chem. 74 2002 821
12. M.C. Aragoni, M. Arca, F. Demartin, F.A. Devillanova, F. Isaia, A. Garau, V. Lippolis, F. Jalali, U. Papke, M. Shamsipur, L. Tei, A. Yari, and G. Verani Inorg. Chem. 41 2002 6623
13. A.B. Descalzo, R. Martínez-Máñez, R. Radeglia, K. Rurack, and J. Sato J. Am. Chem. Soc. 125 2003 3418
14. S.Y. Moon, N.R. Cha, Y.H. Kim, and S.-K. Chang J. Org. Chem. 69 2004 181
15. R. Métivier, I. Leray, and B. Valeur Chem. Eur. J. 10 2004 4480
16. J.H. Kim, A.-R. Hwang, and S.-K. Chang Tetrahedron Lett. 45 2004 7557 and references therein
17. G. Hennrich, H. Sonnenschein, and U. Resch-Gengar J. Am. Chem. Soc. 121 1999 5073
18. L. Prodi, C. Bargossi, M. Montalti, N. Zaccheroni, N. Su, J.S. Bradshaw, R.M. Izatt, and P.B. Savage J. Am. Chem. Soc. 122 2000 6769
19. K. Rurack, U. Resch-Genger, J.L. Bricks, and M. Spieles Chem. Commun. 2000 2103
20. E.M. Nolan, and S.J. Lippard J. Am. Chem. Soc. 125 2003 14270
21. X.F. Guo, X.H. Qian, and L.H. Jia J. Am. Chem. Soc. 126 2004 2272
22. Th. Förster, and K. Kasper Z. Phys. Chem. (Frankfurt am Main) 1 1954 275
23. Th. Förster Angew. Chem. 8 1969 364
24. Th. Förster Angew. Chem. 8 1969 333
25. H. Irngartinger, R.G.H. Kirrstetter, C. Krieger, H. Rodewald, and H.A. Staab Tetrahedron Lett. 1977 1425
26. H.A. Staab, and R.G.H. Kirrstetter Liebigs Ann. Chem. 1979 886
27. A. Ono, and H. Togashi Angew. Chem. Int. Ed. 43 2004 4300