A new Tb3+-selective fluorescent sensor based on 2-(5-(dimethylamino)naphthalen-1-ylsulfonyl)-N-henylhydrazinecarbothioamide

Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy

Volumn 74, Issue 2, 2009, Pages 575-578

  Ganjali, M R ^a,b   Veismohammadi, B ^a   Hosseini, M ^c   Norouzi, P ^a,b  

^a UNIVERSITY OF TEHRAN   (Iran)

^b TEHRAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^c ISLAMIC AZAD UNIVERSITY   (Iran)

Author keywords

Fluorescence; Quenching; Sensor; Tb(III)

Indexed keywords

ASSOCIATION CONSTANT; CHEMOSENSOR; COMPLEX FORMATIONS; CONCENTRATION RANGES; DETECTION LIMITS; FLUORESCENCE QUENCHING; FLUORESCENT EMISSION; FLUORESCENT PROBES; FLUORESCENT SENSORS; HIGH SELECTIVITY; LINEAR RESPONSE RANGE; SELECTIVE DETECTION; TB(III); TERBIUM IONS; TRIVALENT CATIONS;

FLUORESCENCE; METAL IONS; POSITIVE IONS; PROBES; QUENCHING; SENSORS; TERBIUM;

TERBIUM ALLOYS;

2 (5 (DIMETHYLAMINO)NAPHTHALEN 1 YLSULFONYL) N HENYLHYDRAZINECARBOTHIOAMIDE; 2-(5-(DIMETHYLAMINO)NAPHTHALEN-1-YLSULFONYL)-N-HENYLHYDRAZINECARBOTHIOAMIDE; CATION; FLUORESCENT DYE; SULFONAMIDE; TERBIUM; THIOSEMICARBAZONE DERIVATIVE;

ARTICLE; CHEMICAL ANALYSIS; CHEMISTRY; FLUORESCENCE; METHODOLOGY; SENSITIVITY AND SPECIFICITY; SYNTHESIS; VALIDATION STUDY;

CATIONS; CHEMISTRY TECHNIQUES, ANALYTICAL; FLUORESCENCE; FLUORESCENT DYES; SENSITIVITY AND SPECIFICITY; SULFONAMIDES; TERBIUM; THIOSEMICARBAZONES;

EID: 69249208524     PISSN: 13861425     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.saa.2009.07.014     Document Type: Article

References (24)

1. Bekiari V., Judeinstein P., and Lianos P.J. Lumin 104 (2003) 13
2. Xia W.S.H., Schmehl R.H., and Li C.J. Tetrahedron 56 (2000) 7045
3. Jiang W., Feng Y., Ma Y., Wang N., and Si. Z. Anal. Sci. 19 (2003) 923
4. Ricci R.W., and Kilichowski K.B. Anal. Chem. 78 (1974) 1953
5. Brittain H.G. Anal. Chem. 59 (1987) 1122
6. J.R. Lakowicz (Ed). Probe design and chemical sensing, Topics in Fluorescence Spectroscopy, Plenum Press, New York, 74, 1994.
7. de Silva A.P., Gunaratne H.G.N., Gunnlaugsson T., Huxley A.J.M.H., McCoy C.P., Rademacher J.T., and Rice T.E. Chem. Rev. 97 (1997) 1515
8. Valeur B., and Leray I. Coord. Chem. Rev. 205 (2000) 3
9. Zheng H.Z., Liu L., Zhang Z.J., Huang Y.M., Zhou D.B., Hao J.Y., Lu Y.H., and Chen S.M. Spectrochim, Acta part A: Mol. Biomol. Spectrosc. 71 (2009) 1683
10. Shamsipur M., Alizadeh K., Hosseini M., Caltagirone C., and Lippolis V. Sens. Actuators B 113 (2006) 892
11. Zamani H.A., Ganjali M.R., Norouzi P., Tadjarodi A., and Shahsavani E. Mat. Sci. Eng. C 28 (2008) 1489
12. Mathis G., and Clin G. Chemistry 39 (1993) 1953
13. Parker D., and Williams J.A.J. Chem. Soc. Dalton Trans (1996) 3613
14. Denardo G.L., and Mirik G.R.J. Nucl. Med. 37 (1996) 451
15. Bargossi C., Fiorini M.C., Montalti M., Prodi L., Bolletta F., and Zaccheroni N. Coord. Chem. Rev. 208 (2000) 17
16. Chen C.F., and Chen Q.Y. Tetrahedron Lett. 45 (2004) 3957
17. Costa T., Miguel M.D.G., Lindman B., Schillen K., and Seixas de Melo J.S.J. Phys. Chem. B. 109 (2005) 11478
18. Ynag H., Liu Z.-q., Zhou Z.-G., Shi E.-X., Li F.-Y., Du Y.-K., Yu T., and Huang C.-H. Tetrahedron Lett. 47 (2006) 2911
19. Talanova G.G., Elkarim N.S.A., Tanalova V.S., and Bartsch R.A. Anal. Chem. 71 (1999) 3106
20. Stern O., and Volmer M. phys. Z 20 (1919) 183
21. Long G.L., and Winefordner J.D. Anal. Chem. 55 (1983) 712A
22. Burkert U., and Allinger N.L. Molecular Mechanics, ACS Monograph 177 (1982), American Chemical Society, Washington, DC
23. Hyperchem, Release 7.0, Hypercube, Inc., Gainesville, 2002.
24. Stewart J.J.P.J. Comp. Chem. 109 (1989) 209