Effect of substituents on FRET in rhodamine based chemosensors selective for Hg2+ ions

Analyst

Volumn 139, Issue 7, 2014, Pages 1628-1631

  Pal, Siddhartha ^a   Sen, Buddhadeb ^a   Mukherjee, Manjira ^a   Dhara, Koushik ^b   Zangrando, Ennio ^c   Mandal, Sushil Kumar ^d   Khuda Bukhsh, Anisur Rahman ^d   Chattopadhyay, Pabitra ^a  

^a UNIVERSITY OF BURDWAN   (India)

^b Sambhu Nath College   (India)

^c UNIVERSITY OF TRIESTE   (Italy)

^d UNIVERSITY OF KALYANI   (India)

Author keywords

[No Author keywords available]

Indexed keywords

4 ANISALDEHYDE; 4 NITROBENZALDEHYDE; 4-ANISALDEHYDE; 4-NITROBENZALDEHYDE; BENZALDEHYDE DERIVATIVE; DIVALENT CATION; FLUORESCENT DYE; HYDRAZINE DERIVATIVE; MERCURY; RHODAMINE; RHODAMINE B HYDRAZIDE;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; FLUORESCENCE RESONANCE ENERGY TRANSFER; METHODOLOGY;

BENZALDEHYDES; CATIONS, DIVALENT; FLUORESCENCE RESONANCE ENERGY TRANSFER; FLUORESCENT DYES; HYDRAZINES; MERCURY; MOLECULAR STRUCTURE; RHODAMINES;

EID: 84897704499     PISSN: 00032654     EISSN: 13645528     Source Type: Journal    
DOI: 10.1039/c3an02011h     Document Type: Article

References (48)

1. Q. Wang, D. Kim, D. D. Dionysiou, G. A. Sorial, D. Timberlake: Environ. Pollut. 2004 131:323
2. H. Harris, I. Pickering, G. N. George: Science 2003 301:1203
3. L. Patrick: Alternative Med. Rev. 2002 7:456
4. R. Von Burg and M. R. Greenwood, Metals and their Compounds in the Environment, VCH, Weinheim, 1991, pp. 1045-1088
5. E. M. Nolan, S. J. Lippard: Acc. Chem. Res. 2009 42:193
6. J. S. Kim, D. T. Quang: Chem. Rev. 2007 107:3780
7. S. Sen, K. Chakrabarty, I. Hauli, S. K. Mukhopadhyay, P. Chattopadhyay: Org. Biomol. Chem. 2013 11:1537
8. S. Sen, T. Mukherjee, B. Chattopadhyay, A. Moirangthem, A. Basu, J. Marek, P. Chattopadhyay: Analyst 2012 137:3975
9. S. Sen, S. Sarkar, B. Chattopadhyay, A. Moirangthem, A. Basu, K. Dhara, P. Chattopadhyay: Analyst 2012 137:3335
10. S. Sen, T. Mukherjee, S. Sarkar, S. Mukherjee, P. Chattopadhyay: Analyst 2011 136:4839
11. U. C. Saha, K. Dhara, B. Chattopadhyay, S. K. Mandal, S. Mondal, S. Sen, M. Mukherjee, S. van Smaalen, P. Chattopadhyay: Org. Lett. 2011 13:4510
12. U. C. Saha, B. Chattopadhyay, K. Dhara, S. K. Mandal, S. Sarkar, A. R. Khuda-Bukhsh, M. Mukherjee, M. Helliwell, P. Chattopadhyay: Inorg. Chem. 2011 50:1213
13. K. Dhara, U. C. Saha, A. Dan, M. Manassero, S. Sarkar, P. Chattopadhyay: Chem. Commun. 2010 1754
14. U. Basu, I. Khan, A. Hussain, P. Kondaiah, A. R. Chakravarty: Angew. Chem., Int. Ed. 2012 51:2658
15. G. Bunt, F. S. Wouters: Int. Rev. Cytol. 2004 237:205
16. M. Parsons, B. Vojnovic, S. Ameer-Beg: Biochem. Soc. Trans. 2004 32:431
17. E. A. Jares-Erijman, T. M. Jovin: Nat. Biotechnol. 2003 21:1387
18. T. Heyduk: Curr. Opin. Biotechnol. 2002 13:292
19. D. M. Willard, L. L. Carillo, J. Jung, A. V. Orden: Nano Lett. 2001 1:469
20. P. R. Selvin: Nat. Struct. Biol. 2000 7:730
21. V. G. Kozlov, V. Bulovic, P. E. Burrows, S. R. Forrest: Nature 1997 389:362
22. E. R. Chapman, K. Alexander, T. Vorherr, E. Carafoil, D. R. Storm: Biochemistry 1992 31:12819
23. E. Haas, M. Wilchek, E. Katchalski-Katzir, I. Z. Steinberg: Proc. Natl. Acad. Sci. U. S. A. 1975 72:1807
24. L. Yuan, W. Lin, K. Zheng, S. Zhu: Acc. Chem. Res. 2013 46:1462
25. C. Ghatak, V. G. Rao, R. Pramanik, S. Sarkar, N. Sarkar: Phys. Chem. Chem. Phys. 2011 13:3711
26. C. Ma, F. Zeng, L. Huang, S. Wu: J. Phys. Chem. B 2011 115:874
27. Y. H. Lee, M. H. Lee, J. F. Zhang, J. S. Kim: J. Org. Chem. 2010 75:7159
28. S. A. Grant, M. E. Pierce, D. J. Lichlyter, D. A. Grant: Anal. Bioanal. Chem. 2005 381:1012
29. C. Berney, G. Danuser: Biophys. J. 2003 84:3992
30. R. M. Clegg, A. I. H. Murchie, A. Zechel, D. M. J. Lilley: Proc. Natl. Acad. Sci. U. S. A. 1993 90:2994
31. K. G. Rice, P. Wu, L. Brand, Y. C. Lee: Biochemistry 1993 32:7264
32. T. Forster: Ann. Phys. 1948 437:55
33. J. R. Lakowicz, Principles of Fluorescence Spectroscopy, Springer, 2006, pp. 443-447
34. N. J. Turro, Modern Molecular Photochemistry; Benjamin/Cummings Publishing Co., Inc., Menlo Park, CA, 1978
35. X. Chen, T. Pradhan, F. Wang, J. S. Kim, J. Yoon: Chem. Rev. 2012 112:1910
36. M. Vendrell, D. Zhai, J. C. Er, Y. T. Chang: Chem. Rev. 2012 112:4391
37. C. Kar, M. D. Adhikari, A. Ramesh, G. Das: Inorg. Chem. 2013 52:743
38. A. Hakonen: Anal. Chem. 2009 81:4555
39. J. R. Zhang, W. T. Huang, W. Y. Xie, T. Wen, H. Q. Luo, N. B. Li: Analyst 2012 137:3300
40. X. F. Liu, L. K. Miao, X. Jiang, Y. W. Ma, Q. L. Fan, W. Huang: Chin. J. Chem. 2011 29:1031
41. Z. Zhu, L. Xu, X. Zhou, J. G. Qin, C. L. Yang: Chem. Commun. 2011 47:8010
42. B. N. Oh, S. J. Park, J. Ren, Y. J. Jang, S. K. Kim, J. Kim: Dalton Trans. 2011 40:6494
43. L. B. Zhang, T. Li, B. L. Li, J. Li, E. K. Wang: Chem. Commun. 2010 46:1476
44. M. Zhang, B. C. Yi, W. H. Tan, B. C. Ye: Biosens. Bioelectron. 2011 26:3260
45. H. L. Li, J. F. Zhai, X. P. Sun: Nanoscale 2011 3:2155
46. L. Q. Guo, N. Yin, D. D. Nie, J. R. Gan, M. J. Li, F. F. Fu, G. N. Chen: Analyst 2011 136:1632
47. H. A. Benesi, J. H. Hildebrand: J. Am. Chem. Soc. 1949 71:2703
48. A. J. Weerasinghe, C. Schmiesing, E. Sinn: Tetrahedron 2011 67:2833