Relay recognition of Cu2+ and S2- in water by a simple 2-(2′-aminophenyl)benzimidazole derivatized fluorescent sensor through modulating ESIPT

Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy

Volumn 122, Issue , 2014, Pages 656-660

  Tang, Lijun ^a   Dai, Xin ^a   Cai, Mingjun ^a   Zhao, Jia ^a   Zhou, Pei ^a   Huang, Zhenlong ^a  

^a BOHAI UNIVERSITY   (China)

Author keywords

Copper detection; ESIPT; Relay recognition; Sulfide recognition

Indexed keywords

DISPLACEMENT APPROACHES; EMISSION BANDS; ESIPT; EXCITED-STATE INTRAMOLECULAR PROTON TRANSFER; FLUORESCENT SENSORS; RELAY RECOGNITION; SULFIDE RECOGNITION; WATER SOLUTIONS;

FLUORESCENCE; SENSORS;

COPPER COMPOUNDS;

2 (2' AMINOPHENYL)BENZIMIDAZOLE; 2-(2'-AMINOPHENYL)BENZIMIDAZOLE; ANION; BENZIMIDAZOLE DERIVATIVE; COPPER; DIVALENT CATION; FLUORESCENT DYE; SULFIDE; WATER;

ARTICLE; CHEMISTRY; COPPER DETECTION; ESIPT; RELAY RECOGNITION; SPECTROFLUOROMETRY; SULFIDE RECOGNITION;

COPPER DETECTION; ESIPT; RELAY RECOGNITION; SULFIDE RECOGNITION;

ANIONS; BENZIMIDAZOLES; CATIONS, DIVALENT; COPPER; FLUORESCENT DYES; SPECTROMETRY, FLUORESCENCE; SULFIDES; WATER;

EID: 84890448446     PISSN: 13861425     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.saa.2013.11.091     Document Type: Article

References (26)

1. X. Chen, T. Pradhan, F. Wang, J.S. Kim, and J. Yoon Chem. Rev. 112 2012 1910 1956
2. Y. Yang, Q. Zhao, W. Feng, and F. Li Chem. Rev. 113 2013 192 270
3. B. Sarkar Chem. Rev. 99 1999 2535 2544
4. X. Lou, D. Ou, Q. Li, and Z. Li Chem. Commun. 48 2012 8462 8477
5. Hydrogen Sulfide; World Health Organization: Geneva, 1981 (Environmental Health Criteria, No. 19).
6. X. Cao, W. Lin, and L. He Org. Lett. 13 2011 4716 4719
7. G. Zhou, H. Wang, Y. Ma, and X. Chen Tetrahedron 69 2013 867 870
8. P.D. Beer, and P.A. Gale Angew. Chem. Inter. Ed. 40 2001 486 516
9. F. Hou, L. Huang, P. Xi, J. Cheng, X. Zhao, G. Xie, Y. Shi, F. Cheng, X. Yao, and D. Bai Inorg. Chem. 51 2012 2454 2460
10. C. Gao, X. Liu, X. Jin, J. Wu, Y. Xie, W. Liu, X. Yao, and Y. Tang Sens. Actuators B: Chem. 185 2013 125 131
11. M.-Q. Wang, K. Li, J.-T. Hou, M.-Y. Wu, Z. Huang, and X.-Q. Yu J. Org. Chem. 77 2012 8350 8354
12. H. Wang, G. Zhou, and X. Chen Sens. Actuators B: Chem. 176 2013 698 703
13. M.G. Choi, S. Cha, H. Lee, H.L. Jeon, and S.-K. Chang Chem. Commun. 45 2009 7390 7392
14. L. Tang, M. Cai, Z. Huang, K. Zhong, S. Hou, Y. Bian, and R. Nandhakumar Sens. Actuators B: Chem. 185 2013 188 194
15. E.A. Lyakhova, Y.A. Gusyeva, J.V. Nekhoroshkova, L.M. Shafran, and S.A. Lyakhov Eur. J. Med. Chem. 44 2009 3305 3312
16. J. Wu, W. Liu, J. Ge, H. Zhang, and P. Wang Chem. Soc. Rev. 40 2011 3483 3495
17. J. Zhao, S. Ji, Y. Chen, H. Guo, and P. Yang Phys. Chem. Chem. Phys. 14 2012 8803 8817
18. Y. Wu, X. Peng, J. Fan, S. Gao, M. Tian, J. Zhao, and S. Sun J. Org. Chem. 72 2007 62 70
19. Q. Chu, D.A. Medvetz, and Y. Pang Chem. Mater. 19 2007 6421 6429
20. A. Helal, N.T.T. Thao, S.W. Lee, and H.-S. Kim J. Incl. Phenom. Macro. Chem. 66 2009 87 94
21. H.S. Jung, H.J. Kim, J. Vicens, and J.S. Kim Tetrahedron Lett. 50 2009 983 987
22. S. Santra, G. Krishnamoorthy, and S.K. Dogra J. Phys. Chem. A. 104 2000 476 482
23. Y. Shiraishi, Y. Matsunaga, and T. Hirai J. Phys. Chem. A 117 2013 3387 3395
24. M. Chen, X. Lv, Y. Liu, Y. Zhao, J. Liu, P. Wang, and W. Guo Org. Biomol. Chem. 9 2011 2345 2349
25. C.-H. Hung, G.-F. Chang, A. Kumar, G.-F. Lin, L.-Y. Luo, W.-M. Ching, and E.W.-G. Diau Chem. Commun. 44 2008 978 980
26. E. Hao, T. Meng, M. Zhang, W. Pang, Y. Zhou, and L. Jiao J. Phys. Chem. A. 115 2011 8234 8241