Highly reactive (<1 min) ratiometric probe for selective 'naked-eye' detection of cyanide in aqueous media

Tetrahedron Letters

Volumn 54, Issue 14, 2013, Pages 1785-1789

  Goswami, Shyamaprosad ^a   Manna, Abhishek ^a   Paul, Sima ^a   Aich, Krishnendu ^a   Das, Avijit Kumar ^a   Chakraborty, Shampa ^a  

^a INDIAN INSTITUTE OF ENGINEERING SCIENCE AND TECHNOLOGY   (India)

Author keywords

Benzothiazole; Cyanide; Naked eye detection; Ratiometric; Sensor; Triphenylamine

Indexed keywords

BENZOTHIAZOLE DERIVATIVE; CYANIDE; TRIPHENYLAMINE BENZOTHIAZOLE; UNCLASSIFIED DRUG;

AQUEOUS SOLUTION; ARTICLE; COLORIMETRY; DENSITY FUNCTIONAL THEORY; REACTION TIME; ROOM TEMPERATURE; SENSOR; SPECTROSCOPY; SYNTHESIS;

EID: 84875211499     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2012.12.092     Document Type: Article

References (44)

1. P.D. Beer, and P.A. Gale Angew. Chem., Int. Ed. 40 2001 486
2. R. Martinez-Manez, and F. Sancenon Chem. Rev. 103 2003 4419
3. T. Gunnlaugsson, M. Glynn, G.M. Tocci, P.E. Kruger, and F.M. Pfeffer Coord. Chem. Rev. 250 2006 3094
4. J.L. Sessler, P.A. Gale, and W.S. Cho Anion Receptor Chemistry 2006 Royal Society of Chemistry Cambridge
5. G.W. Bates, Triyanti, Mark E. Light, M. Albrecht, and P.A. Gale J. Org. Chem. 72 2007 8921 8927
6. J.L. Sessler, G.D. Pantos, P.A. Gale, and M.E. Light Org. Lett. 8 2006 1593 1596
7. N. Busschaert, M. Wenzel, M.E. Light, P. Iglesias-Hernandez, R. Perez-Tomas, and P.A. Gale J. Am. Chem. Soc. 133 2011 14136 14148
8. M.T. Albelda, J.C. Frías, E. Garcia-España, and H.-J. Schneider Chem. Soc. Rev. 41 2012 3859 3877
9. E. Delgado-Pinar, C. Rotger, A. Costa, M. Neus Pin, R.J. Hermas, J. Alarcon, and E. Garcia-España Chem. Commun. 48 2012 2609 2611
10. J.L. Sessler, D.E. Gross, W.-S. Cho, V.M. Lynch, F.P. Schmidtchen, G.W. Bates, M.E. Light, and P.A. Gale J. Am. Chem. Soc. 128 2006 12281 12288
11. S.I. Baskin, and T.G. Brewer F. Sidell, E.T. Takafuji, D.R. Franz, Medical Aspects of Chemical and Biological Warfare 1997 TMM Publications Washington DC 271 286
12. Eisler, R.; In Cyanide Hazards to Fish, Wildlife, and Invertebrates: A 80 Synoptic Review; U.S. Fish Wildl. Serv. Biol. Rep., 85 (1991), (1.23).
13. B.E. Vennesland, E. Comm, C.J. Knownles, J. Westly, and F. Wissing Cyanide in Biology 1981 Academic Press London
14. G.D. Muir Hazards in the Chemical Laboratory 1977 The Royal Chemical Society London
15. Dekant, W.; Vamvakas, s. Ullmann's Encyclopedia of Industrial Chemistry, 6th ed., Wiley-VCH, New York, 1999.
16. Miller, G.C.; Pritsos, C.A.; Cyanide, Proceedings Symposium Annual Meeting, TMS, San Diego, California: USA, 2001, pp 73-81.
17. H. Sun, Y.Y. Zhang, S.H. Si, D.R. Zhu, and Y.S. Fung Sens. Actuators B 108 2005 925 932
18. Y.-H. Kim, and J.-I. Hong Chem. Commun. 2002 512
19. C.F. Chow, M.H.W. Lam, and W.Y. Wong Inorg. Chem. 43 2004 8387
20. J.V. Ros-Lis, R. Martinez-Manez, and J. Soto Chem. Commun. 2005 5260
21. W.J. Jin, M.T. Fernandez-Arguelles, J.M. Costa-Fernandez, J.M.R. Pereiro, and A. Sanz-Medel Chem. Commun. 2005 883
22. P. Anzenbacher, D.S. Tyson Jr., K. Jursíková, and F.N. Castellano J. Am. Chem. Soc. 124 2002 6232
23. H. Miyaji, and J.L. Sessler Angew. Chem., Int. Ed. 40 2001 154
24. S.-Y. Chung, S.-W. Nam, J. Lim, S. Park, and J. Yoon Chem. Commun. 2009 2866
25. X. Lou, L. Qiang, J. Qin, and Z. Li ACS Appl. Mater. Interfaces 1 2009 2529
26. H.S. Jung, J.H. Han, Z.H. Kim, C. Kang, and J.S. Kim Org. Lett. 13 2011 5056 5059
27. M.R. Ajayakumar, and P. Mukhopadhyay Org. Lett. 12 2010 2646
28. M. Tomasulo, and F.M. Raymo Org. Lett. 7 2005 4633
29. M. Tomasulo, S. Sortino, A.J.P. White, and F.M. Raymo J. Org. Chem. 71 2006 744
30. F. García, J.M. García, B. García-Acosta, R. Martínez-Máñez, F. Sancenón, and J. Soto Chem. Commun. 22 2005 2790
31. J.V. Ros-Lis, R. Martínez-Máñez, and J. Soto Chem. Commun. 19 2002 2248
32. H. Lee, Y.M. Chung, and K.H. Ahn Tetrahedron Lett. 49 2008 5544
33. H. Miyaji, D.-S. Kim, B.-Y. Chang, E. Park, S.-M. Park, and K.H. Ahn Chem. Commun. 6 2008 753
34. Y. Chung, H. Lee, and K.H. Ahn J. Org. Chem. 71 2006 9470
35. Y.-K. Yang, and J. Tae Org. Lett. 8 2006 5721
36. K.-S. Lee, J.T. Lee, J.-I. Hong, and H.-J. Kim Chem. Lett. 36 2007 816
37. K.-S. Lee, H.-J. Kim, G.-H. Kim, I. Shin, and J.-I. Hong Org. Lett. 10 2008 49
38. Z. Ekmekci, M.D. Yilmaz, and E.U. Akkaya Org. Lett. 10 2008 461
39. L. Peng, M. Wang, G. Zhang, D. Zhang, and D. Zhu Org. Lett. 11 2009 1943
40. H.-T. Niu, X. Jiang, J. He, and J.-P. Cheng Tetrahedron Lett. 49 2008 6521
41. G. Lai, X.R. Bu, J. Santos, and E.A. Mintz Synlett 1997 1275
42. H.Y. Lee, M. Chung, and K.H. Ahn Tetrahedron Lett. 49 2008 5544 5547
43. S.-X. Guo, J. Xie, R. Gilbert-Wilson, S.L. Birkett, A.M. Bond, and A.G. Wedd Dalton Trans. 40 2011 356 366
44. T. Stanoeva, D. Neshchadin, G. Gescheidt, J. Ludvik, B. Lajoie, and S.N. Batchelor J. Phys. Chem. A 109 2005 11103 11110