An azo dye-coupled tripodal chromogenic sensor for cyanide

Tetrahedron Letters

Volumn 52, Issue 51, 2011, Pages 6919-6922

  Lee, Doo Youn ^a   Singh, Narinder ^b   Satyender, Apuri ^a   Jang, Doo Ok ^a  

^a Yonsei University Wonju   (South Korea)

^b INDIAN INSTITUTE OF TECHNOLOGY ROPAR   (India)

Author keywords

Azo dye; Chemosensor; Chromogenic; Cyanide; Tripodal receptor

Indexed keywords

ANION; AZO DYE; CYANIDE;

ARTICLE; BINDING AFFINITY; HYDROGEN BOND; SENSOR; SIGNAL TRANSDUCTION; SYNTHESIS;

EID: 81255175656     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2011.10.061     Document Type: Article

References (29)

1. W.I.B. White, D.I. Arias-Garzon, J.M. McMahon, and R.T. Sayre Plant Physiol. 116 1998 1219 1225
2. J.E. Poulton Plant Physiol. 94 1990 401 405
3. Kulig, K. W. Cyanide Toxicity; U.S. Department of Health and Human Services: Atlanta, 1991.
4. rd Ed.; World Health Organization: Geneva, 2008; Vol. 1, Chapter 8.
5. M.T. Wilson, G. Antoninin, R. Malatestan, P. Sartin, and M. Brunorin J. Biol. Chem. 269 1994 24114 24119
6. A.V. Gourinel, N. Dale, E. Llaudet, D.M. Poputnikov, K.M. Spyer, and V.N. Gourine J. Physiol. 585 2007 305 316
7. T. Suzuki, A. Hiolki, and M. Kurahashi Anal. Chim. Acta 476 2003 159 165
8. D. Shan, C. Mousty, and S. Cosnier Anal. Chem. 76 2004 178 183
9. V.R. Rao, S.R. Suresh, N.B.S.N. Rao, and P. Rajaram Bull. Electrochem. 13 1997 327 329
10. T.T. Christison, and J.S. Rohrer J. Chromatogr. A 1155 2007 31 39
11. Y.G. Timofeyenko, J.J. Rosentreter, and S. Mayo Anal. Chem. 79 2007 251 255
12. C. Giuriati, S. Cavalli, A. Gorni, D. Badocco, and P. Pastore J. Chromatogr. A. 1023 2004 105 112
13. Z. Xu, X. Chen, H.N. Kim, and J. Yoon Chem. Soc. Rev. 39 2010 127 137
14. J. Isaad, and A.E. Achari Analytica Chim. Acta 694 2011 120 127
15. J. Isaad, and A.E. Achari Tetrahedron 67 2011 5678 5685
16. J. Isaad, and A.E. Achari Tetrahedron 67 2011 4939 4947
17. J. Isaad, and A.E. Achari Tetrahedron 67 2011 4196 4201
18. J. Isaad, and A. Perwuelz Tetrahedron Lett. 51 2010 5810 5814
19. I.S. Park, E.-J. Heo, and J.-M. Kim Tetrahedron Lett. 52 2011 2454 2457
20. Z. Xu, J. Pan, D.R. Spring, J. Cui, and J. Yoon Tetrahedron 66 2010 1678 1683
21. X. Chen, S.-W. Nam, G.-H. Kim, N. Song, Y. Jeong, I. Shin, S.K. Kim, J. Kim, S. Park, and J. Yoon Chem. Commun. 46 2010 8953 8955
22. K. Poland, E. Topoglidis, J.R. Durrant, and E. Palomares Inorg. Chem. Commun. 9 2006 1239 1242
23. M.O. Odagoa, D.M. Colabelloa, and A.J. Lees Tetrahedron 66 2010 7465 7471
24. A. Aldrey, C. Núñez, V. García, R. Bastida, C. Lodeiro, and A. Macías Tetrahedron 66 2010 9223 9230
25. V. Kumar, M.P. Kaushik, A.K. Srivastava, A. Pratap, V. Thiruvenkatam, and T.N. Guru Row Anal. Chim. Acta 663 2010 77 84
26. V.K. Bhardwaj, M.S. Hundal, and G. Hundal Tetrahedron 65 2009 8556 8562
27. D.Y. Lee, N. Singh, M.J. Kim, and D.O. Jang Org. Lett. 13 2011 3024 3027
28. P. Job Ann. Chim. 9 1928 113 203
29. H. Benesi, and H. Hildebrand J. Am. Chem. Soc. 71 1949 2703 2707