Synthesis of porphyrin-appended terpyridine as a chemosensor for cadmium based on fluorescent enhancement

Talanta

Volumn 72, Issue 2, 2007, Pages 575-581

  Luo, Hong Yuan ^a   Jiang, Jian Hui ^a   Zhang, Xiao Bing ^a   Li, Chun Yan ^a   Shen, Guo Li ^a   Yu, Ru Qin ^a  

^a HUNAN UNIVERSITY   (China)

Author keywords

Cadmium ions; Chelation enhanced fluorescence effect; Photoinduced electron transfer; Porphyrin terpyridine

Indexed keywords

CADMIUM; CHARGE TRANSFER; FLUORESCENCE; PORPHYRINS; SYNTHESIS (CHEMICAL);

CADMIUM IONS; CHELATION-ENHANCED FLUORESCENCE EFFECT; PHOTOINDUCED ELECTRON TRANSFER; PORPHYRIN-TERPYRIDINE;

CHEMICAL SENSORS;

EID: 34047247331     PISSN: 00399140     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.talanta.2006.11.028     Document Type: Article

References (33)

1. Dobson S. Cadmium-Environmental Aspects (1992), World Health Organization, Geneva
2. Rama M.J.R., Medina A.R., and Díaz A.M. Talanta 66 (2005) 1333
3. Yu Y., Lin L.R., Yang K.B., Zhong X., Huang R.B., and Zheng L.S. Talanta 69 (2006) 103
4. Kimura E., and Koike T. Chem. Soc. Rev. 27 (1998) 179
5. He C.L., Ren F.L., Zhang X.B., and Han Z.X. Talanta 70 (2006) 364
6. Lim N.C., Freake H.C., and Brückner C. Chem. Eur. J. 11 (2005) 38
7. Hefley A.J. Anal. Chem. 46 (1974) 2036
8. Hennrich G., Sonnenschein H., and Resch-Genger U. J. Am. Chem. Soc. 121 (1999) 5073
9. Gunnlaugsson T., Lee T.C., and Parkesh R. Org. Lett. 5 (2003) 4065
10. Charles S., Dubois F., Yunus S., and Donckt E.V. J. Fluoresc. 10 (2000) 99
11. Herbich J., Kijak M., Zielińska A., Thummel R.P., and Waluk J. J. Phys. Chem. A 106 (2002) 2158
12. Waluk J. Acc. Chem. Res. 36 (2003) 832
13. Clements J.H., and Webber S.E. Macromolecules 37 (2004) 1531
14. Kruper, Chamberlin T.A., and Kochanny M. J. Org. Chem. 54 (1989) 2753
15. Fallahpour R.A. Synthesis 8 (2000) 1138
16. Flamigni L., Barigelletti F., Armaroli N., Collin J.-P., Sauvage J.-P., and Williams J.A.G. Chem. Eur. J. 4 (1998) 1744
17. Collin J.-P., Harriman A., Heitz V., Odobel F., and Sauvage J.-P. J. Am. Chem. Soc. 116 (1994) 5679
18. Husson J., Beley M., and Kirsch G. Tetrahedron Lett. 44 (2003) 1767
19. Cave G.W.V., and Raston C.L. J. Chem. Soc., Perkin Trans. 1 (2001) 3258
20. Yu Y., Ostresh J.M., and Houghten R.A. J. Org. Chem. 67 (2002) 5831
21. Seybold P.G., and Gouterman M. J. Mol. Spectrosc. 31 (1969) 1
22. Okamoto K., and Fukuzumi S. J. Am. Chem. Soc. 126 (2004) 13922
23. Kuciauskas D., Liddell P.A., Hung S.-C., Lin S., Stone S., Seely G.R., Moore A.L., Moore T.A., and Gust D. J. Phys. Chem. B 101 (1997) 429
24. Reddy D., and Chandrashekar T.K. J. Chem. Soc. Dalton Trans. (1992) 619
25. Hill M.G., Bailey J.A., Miskowski V.M., and Gray H.B. Inorg. Chem. 35 (1996) 4585
26. Zheng Y., Cao X., Orbulescu J., Konka V., Andreopoulos F.M., Pham S.M., and Leblanc R.M. Anal. Chem. 75 (2003) 1706
27. de Silva A.P., Gunaratne H.Q.N., and Maguire G.E.M. J. Chem. Soc., Chem. Commun. (1994) 1213
28. Reany O., Gunnlaugsson T., and Parker D. J. Chem. Soc., Perkin Trans. 2 (2000) 1819
29. Bissell R.A., de Silva A.P., Gunaratne H.Q.N., Lynch P.L.M., Maguire G.E.M., McCoy C.P., and Sandanayake K.R.A.S. Top. Curr. Chem. 168 (1993) 223
30. Huston M.E., Haider K.W., and Czarnik A.W. J. Am. Chem. Soc. 110 (1988) 4460
31. Akins D.L., Zhu H.-R., and Guo C. J. Phys. Chem. 100 (1996) 5420
32. Kim K.-Y., and Nancollas G.H. J. Phys. Chem. 81 (1977) 948
33. Nazeeruddin Md.K., Zakeeruddin S.M., Humphry-Baker R., Kaden T.A., and Grätzel M. Inorg. Chem. 39 (2000) 4542