An efficient probe for rapid detection of cyanide in water at parts per billion levels and naked-eye detection of endogenous cyanide

Chemistry - An Asian Journal

Volumn 9, Issue 3, 2014, Pages 830-837

  Kumari, Namita ^a   Jha, Satadru ^a,c   Bhattacharya, Santanu ^a,b  

^a INDIAN INSTITUTE OF SCIENCE   (India)

^b JAWAHARLAL NEHRU CENTRE FOR ADVANCED SCIENTIFIC RESEARCH   (India)

^c SIKKIM MANIPAL INSTITUTE OF TECHNOLOGY   (India)

Author keywords

colorimetric probes; cyanide; Michael addition; oxidation; sensors

Indexed keywords

CYANIDE; MICELLE; MOLECULAR PROBE; WATER;

ANALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; COLOR; HUMAN; LIMIT OF DETECTION; MANIHOT; MICELLE; MOLECULAR PROBE; OBSERVATION; PH; PROCEDURES; SYNTHESIS; TEMPERATURE;

COLOR; CYANIDES; HUMANS; HYDROGEN-ION CONCENTRATION; LIMIT OF DETECTION; MANIHOT; MICELLES; MOLECULAR PROBES; MOLECULAR STRUCTURE; OBSERVATION; TEMPERATURE; WATER;

EID: 84894554650     PISSN: 18614728     EISSN: 1861471X     Source Type: Journal    
DOI: 10.1002/asia.201301390     Document Type: Article

References (78)

1. R. Koenig, Science 2000, 287, 1737.
2. B. Vennesland, E. E. Comm, C. J. Knownles, J. Westly, F. Wissing, Cyanide in Biology, Academic Press, London, 1981.
3. Ullmann's Encyclopedia of Industrial Chemistry, 6th ed., Wiley-VCH, New York, 1999.
4. S. K. Dubey, D. S. Holmes, J. Microb. Biotechnol. 1995, 11, 257.
5. K. Kaur, R. Saini, A. Kumar, V. Luxami, N. Kaur, P. Singh, S. Kumar, Coord. Chem. Rev. 2012, 256, 1992.
6. Z. Xu, X. Chen, H. N. Kim, J. Yoon, Chem. Soc. Rev. 2010, 39, 127.
7. www.epa.gov/safewater/mcl.html#mcls web page.
8. M. A. Santana, V. Vásquez, J. Matehus, R. R. Aldao, Plant Physiol. 2002, 129, 1686.
9. F. H. Zelder, C. Männel-Croisé, Chimia 2009, 63, 58.
10. N. Kumari, S. Jha, S. Bhattacharya, J. Org. Chem. 2011, 76, 8215.
11. I. S. Park, E.-J. Heo, J.-M. Kim, Tetrahedron Lett. 2011, 52, 2454.
12. H. Miyaji, J. L. Sessler, Angew. Chem. 2001, 113, 158
13. Angew. Chem. Int. Ed. 2001, 40, 154.
14. P. Anzenbacher, Jr., K. Jursikova, D. Aldakov, M. Marquez, R. Pohl, Tetrahedron 2004, 60, 11163.
15. P. Anzenbacher, Jr., D. S. Tyson, K. Jursíková, F. N. Castellano, J. Am. Chem. Soc. 2002, 124, 6232.
16. S.-S. Sun, A. J. Lees, Chem. Commun. 2000, 1687.
17. D. Senapati, S. S. R. Dasary, A. K. Singh, T. Senapati, H. Yu, P. C. Ray, Chem. Eur. J. 2011, 17, 8445.
18. X. Lou, Y. Zhang, J. Qin, Z. Li, Chem. Eur. J. 2011, 17, 9691.
19. C.-Y. Liua, W.-L. Tseng, Chem. Commun. 2011, 47, 2550.
20. Q. Zeng, P. Cai, Z. Li, J. Qina, B. Z. Tang, Chem. Commun. 2008, 1094.
21. Y. H. Kim, J. I. Hong, Chem. Commun. 2002, 512.
22. X. Chen, S.-W. Nam, G.-H. Kim, N. Song, Y. Jeong, I. Shin, S. K. Kim, J. Kim, S. Park, J. Yoon, Chem. Commun. 2010, 46, 8953.
23. C.-F. Chow, M. H. W. Lam, W.-Y. Wong, Inorg. Chem. 2004, 43, 8387.
24. J. H. Lee, A. R. Jeong, I.-S. Shin, H.-J. Kim, J.-I. Hong, Org. Lett. 2010, 12, 764.
25. C. R. Wade, F. P. Gabbai, Inorg. Chem. 2010, 49, 714.
26. H. S. Jung, J. H. Han, Z. H. Kim, C. Kang, J. S. Kim, Org. Lett. 2011, 13, 5056.
27. W. J. Jin, M. T. Fernndez-Argelles, J. M. Costa-Fernndez, R. Pereiro, A. Sanz-Medel, Chem. Commun. 2005, 883.
28. X. Cheng, Y. Zhao, J. Qin, Z. Li, ACS Appl. Mater. Interfaces 2012, 4, 2133.
29. Y. Kim, H.-S. Huh, M. H. Lee, I. L. Lenov, H. Zhao, F. P. Gabbabox drawings light down and left, Chem. Eur. J. 2011, 17, 2057.
30. L. Yuan, W. Lin, Y. Yang, J. Song, J. Wang, Org. Lett. 2011, 13, 3730.
31. S.-J. Hong, J. Yoo, S.-H. Kim, J. S. Kim, J. Yoon, C.-H. Lee, Chem. Commun. 2009, 189.
32. Y. Sun, G. Wang, W. Guo, Tetrahedron 2009, 65, 3480.
33. J. L. Sessler, D.-G. Cho, Org. Lett. 2008, 10, 73.
34. D.-G. Cho, J. H. Kim, J. L. Sessler, J. Am. Chem. Soc. 2008, 130, 12163.
35. Z. Ekmekci, M. D. Yilmaz, E. U. Akkaya, Org. Lett. 2008, 10, 461.
36. K.-S. Lee, H.-J. Kim, G.-H. Kim, I. Shin, J.-I. Hong, Org. Lett. 2008, 10, 49.
37. T. W. Hudnall, F. P. Gabbabox drawings light down and left, J. Am. Chem. Soc. 2007, 129, 11978.
38. C.-L. Chen, Y.-H. Chen, C.-Y. Chen, S.-S. Sun, Org. Lett. 2006, 8, 5053.
39. Y.-K. Yang, J. Tae, Org. Lett. 2006, 8, 5721.
40. M. Tomasulo, S. Sortino, A. J. P. White, F. M. Raymo, J. Org. Chem. 2006, 71, 744.
41. J. V. Ros-Lis, R. Martbox drawings light down and leftnez-Manez, J. Soto, Chem. Commun. 2005, 5260.
42. M. Tomasulo, S. Sortino, A. J. P. White, F. M. Raymo, J. Org. Chem. 2005, 70, 8180.
43. L. Wang, X. He, Y. Guo, J. Xu, S. Shao, Beilstein J. Org. Chem. 2011, 7, 218.
44. R. Martínez, A. Espinosa, A. Tarraga, P. Molina, Tetrahedron 2008, 64, 2184.
45. J. W. Lee, S. Y. Park, B.-K. Cho, J. S. Kim, Tetrahedron Lett. 2007, 48, 2541.
46. J. L. Sessler, D.-G. Cho, V. Lynch, J. Am. Chem. Soc. 2006, 128, 16518.
47. X. He, S. Hu, K. Liu, Y. Guo, J. Xu, S. Shao, Org. Lett. 2006, 8, 333.
48. H. J. Kim, H. Lee, J. H. Lee, D. H. Choi, J. H. Jung, J. S. Kim, Chem. Commun. 2011, 47, 10918.
49. N. Kumari, S. Jha, S. Bhattacharya, Chem. Asian J. 2012, 7, 2805.
50. T. Gõmez, D. Moreno, B. Diaz de Grenu, A. G. Fernandez, T. Rodriguez, J. Rojo, J. V. Cuevas, T. Torroba, Chem. Asian J. 2013, 8, 1271.
51. C. Männel-Croisé, F. Zelder, ACS Appl. Mater. Interfaces 2012, 4, 725.
52. C. Männel-Croisé, B. Probst, F. Zelder, Anal. Chem. 2009, 81, 9493.
53. K. P. Divya, S. Sreejith, B. Balakrishna, P. Jayamurthy, P. Anees, A. Ajayaghosh, Chem. Commun. 2010, 46, 6069.
54. C. Agatemor, EJEAFChe 2009, 8, 189.
55. E. Ballesteros, D. Moreno, T. Gomez, T. Rodrbox drawings light down and leftguez, J. Rojo, M. Garcbox drawings light down and lefta-Valverde, T. Torroba, Org. Lett. 2009, 11, 1269.
56. N. Kumari, N. Dey, S. Jha, S. Bhattacharya, ACS Appl. Mater. Interfaces 2013, 5, 2438
57. S. Bhattacharya, N. Kumari, Coord. Chem. Rev. 2009, 253, 2133.
58. J. Hu, L. Dai, S. Liu, Macromolecules 2011, 44, 4699.
59. J. Hu, C. Li, S. Liu, Langmuir 2010, 26, 724.
60. V. S. Jisha, A. J. Thomas, D. Ramaiah, J. Org. Chem. 2009, 74, 6667.
61. P. Pallavicini, L. Pasotti, S. Patroni, Dalton Trans. 2007, 5670.
62. S. Bhattacharya, K. Snehalatha, Langmuir 1995, 11, 4653.
63. P. Pallavicini, Y. A. Diaz-Fernandez, F. Foti, C. Mangano, S. Patroni, Chem. Eur. J. 2007, 13, 178.
64. J. Wang, X. Qian, J. Qian, Y. Xu, Chem. Eur. J. 2007, 13, 7543.
65. Y. Zhao, Z. Zhong, Org. Lett. 2006, 8, 4715.
66. A. Mallick, M. C. Mandal, B. Haldar, A. Chakrabarty, P. Das, N. Chattopadhyay, J. Am. Chem. Soc. 2006, 128, 3126.
67. Y. Nakahara, T. Kida, Y. Nakatsuji, M. Akashi, Org. Biomol. Chem. 2005, 3, 1787.
68. Y. Diaz Fernandez, A. P. Gramatges, V. Amendola, F. Foti, C. Mangano, P. Pallavicini, S. Patroni, Chem. Commun. 2004, 1650.
69. S. Bhattacharya, A. Gulyani, Chem. Commun. 2003, 1158.
70. R. Villamil-Ramos, V. Barba, A. K. Yatsimirsky, Analyst 2012, 137, 5229.
71. R. Hu, J. Feng, D. Hu, S. Wang, S. Li, Y. Li, G. Yang, Angew. Chem. 2010, 122, 5035
72. Angew. Chem. Int. Ed. 2010, 49, 4915.
73. T. Ábalos, S. Royo, R. Martbox drawings light down and leftnez-Manez, F. Sancenon, J. Soto, A. M. Costero, S. Gil, M. Parra, New J. Chem. 2009, 33, 1641.
74. A. L. Koner, J. Schatz, W. M. Nau, U. Pischel, J. Org. Chem. 2007, 72, 3889.
75. K. Niikura, E. V. Anslyn, J. Org. Chem. 2003, 68, 10156.
76. R. P. Paradkar, R. R. Williams, Anal. Chem. 1994, 66, 2752.
77. G. P. Gorbenko, N. O. Mchedlov-Petrossyan, T. A. Chernaya, J. Chem. Soc. Faraday Trans. 1998, 94, 2117.
78. N. Phambu, A. S. Meya, E. B. Djantou, E. N. Phambu, P. Kita-Phambu, L. M. Anovitz, J. Agric. Food Chem. 2007, 55, 10135.