A new colorimetric and fluorescent ratiometric sensor for Hg 2+ based on 4-pyren-1-yl-pyrimidine

Tetrahedron

Volumn 68, Issue 14, 2012, Pages 3129-3134

  Weng, Jiena ^a   Mei, Qunbo ^a   Ling, Qidan ^a   Fan, Quli ^a   Huang, Wei ^a  

^a NANJING UNIVERSITY OF POSTS AND TELECOMMUNICATIONS   (China)

Author keywords

Chemosensor; Hg 2+; Pyrene; Pyrimidine

Indexed keywords

4 PYREN 1 YL PYRIMIDINE; ACETONITRILE; FLUORESCENT DYE; MERCURY; METAL ION; PYRENE; PYRIMIDINE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; COLORIMETRY; DOSIMETER; FLUORESCENCE; PRIORITY JOURNAL; ULTRAVIOLET RADIATION;

EID: 84862778492     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2011.12.071     Document Type: Article

References (61)

1. T. Schrader, and A. Hamilton Functional Synthetic Receptors 2005 John Wiley New York, NY
2. E.V. Anslyn J. Org. Chem. 72 2007 687 699
3. R.A.P. de Silva, T. Gunnlaugsson, and C.P. McCoy J. Chem. Educ. 74 1997 53 58
4. B. Bodenant, T. Weil, M. Businelli-Pourcel, F. Fages, B. Barbe, I. Pianet, and M. Laguerre J. Org. Chem. 64 1999 7034 7039
5. M. Nadal, M. Schuhmacher, and J.L. Domingo Sci. Total Environ. 321 2004 59 69
6. W.F. Fitzgerald, C.H. Lamgorg, and C.R. Hammerschmidt Chem. Rev. 107 2007 641 662
7. C.J. Koester Anal. Chem. 77 2005 3737 3754
8. S.D. Richardson, and T.A. Ternes Anal. Chem. 77 2005 3807 3838
9. P. Chen, and C. He J. Am. Chem. Soc. 126 2004 728 729
10. A. Ono, and H. Togashi Angew. Chem., Int. Ed. 43 2004 4300 4302
11. B. Liu, and H. Tian Chem. Commun. 2005 3156 3158
12. J.S. Wu, I.C. Hwang, K.S. Kim, and J.S. Kim Org. Lett. 9 2007 907 910
13. E.M. Nolan, and S.J. Lippard Chem. Rev. 108 2008 3443 3480
14. X. Chen, K.H. Baek, Y. Kim, S.J. Kim, I. Shin, and J. Yoon Tetrahedron 66 2010 4016 4021
15. P. Mahato, A. Ghosh, S. Saha, S. Mishra, S.K. Mishra, and A. Das Inorg. Chem. 49 2010 11485 11492
16. C.R. Lohani, J.M. Kim, and K.H. Lee Tetrahedron 67 2011 4130 4136
17. F.M. Winnik Chem. Rev. 93 1993 587 614
18. S. Nishzawa, Y. Kato, and N. Teramae J. Am. Chem. Soc. 121 1999 9463 9464
19. D. Sahoo, V. Narayanaswami, C.M. Kay, and R.O. Ryan Biochemistry 39 2000 6594 6601
20. S.J. Kim, K.H. Noh, S.H. Lee, S.K. Kim, S.K. Kim, and J. Yoon J. Org. Chem. 68 2003 597 600
21. H. Yuasa, N. Miyagawa, T. Izumi, M. Nakatani, M. Izumi, and H. Hashimoto Org. Lett. 6 2004 1489 1492
22. S.Y. Moon, N.J. Youn, S.M. Park, and S.K. Chang J. Org. Chem. 70 2005 2394 2397
23. E.J. Jun, H.N. Won, J.S. Kim, K.H. Lee, and J. Yoon Tetrahedron Lett. 47 2006 4577 4580
24. S.M. Park, M.H. Kim, J.I. Choe, K.T. No, and S.K. Chang J. Org. Chem. 72 2007 3550 3553
25. L. Fabbrizzi, and A. Poggi Chem. Soc. Rev. 24 1995 197 202
26. J.B. Birks Photophysics of Aromatic Molecules 1970 Wiley Inter-Science London
27. Y. Shiraishi, Y. Tokitoh, and T. Hirai Org. Lett. 8 2006 3841 3844
28. H.J. Kim, J. Hong, A. Hong, S. Ham, J.H. Lee, and J.S. Kim Org. Lett. 10 2008 1963 1966
29. H.S. Jung, M. Park, D.Y. Han, E. Kim, C. Lee, S. Ham, and J.S. Kim Org. Lett. 11 2009 3378 3381
30. J.S. Kim, M.G. Choi, K.C. Song, K.T. No, S. Ahn, and S.K. Chang Org. Lett. 9 2007 1129 1132
31. S.Y. Park, J.H. Yoon, C.S. Hong, R. Souane, J.S. Kim, S.E. Matthews, and J. Vicens J. Org. Chem. 73 2008 8212 8218
32. Y. Zhou, C.Y. Zhu, X.S. Gao, X.Y. You, and C. Yao Org. Lett. 12 2010 2566 2569
33. M. Kumar, R. Kumar, and V. Bhalla Org. Lett. 13 2011 366 369
34. R. Martínez, A. Espinosa, A. Tárraga, and P. Molina Tetrahedron 66 2010 3662 3667
35. C. Hou, Y. Xiong, N. Fu, C.C. Jacquot, T.C. Squier, and H. Cao Tetrahedron Lett. 52 2011 2692 2696
36. X. Liu, X. Yang, Y. Fu, C. Zhu, and Y. Cheng Tetrahedron 2011 3181 3186
37. A. Caballero, R. Martínez, V. Lloveras, I. Ratera, J. Vidal-Gancedo, K. Wurst, A. Tárraga, P. Molina, and J. Veciana J. Am. Chem. Soc. 127 2005 15666 15667
38. R. Martínez, F. Zapata, A. Caballero, A. Espinosa, A. Tárraga, and P. Molina Org. Lett. 8 2006 3235 3238
39. B. Valeur, and I. Leray Coord. Chem. Rev. 205 2000 3 40
40. H. Nohta, H. Satozono, K. Koiso, H. Yoshida, J. Ishida, and M. Yamaguchi Anal. Chem. 72 2000 4199 4202
41. A. Okamoto, T. Ichiba, and I. Saito J. Am. Chem. Soc. 126 2004 8364 8365
42. A. Ojida, Y. Mito-oka, K. Sada, and I. Humachi J. Am. Chem. Soc. 126 2004 2454 2463
43. Y. Cao, Q. Zheng, C. Chen, and Z. Huang Tetrahedron Lett. 44 2003 4751 4755
44. A. Coskun, M.D. Yilmaz, and E.U. Akkaya Org. Lett. 9 2007 607 609
45. L. Liu, G. Zhang, J. Xiang, D. Zhang, and D. Zhu Org. Lett. 10 2008 4581 4584
46. Z. Li, X. Lou, H. Yu, Z. Li, and J. Qin Macromolecules 41 2008 7433 7439
47. Y. Wan, W. Niu, W.J. Behof, Y. Wang, P. Boyle, and C.B. Gorman Tetrahedron 65 2009 4293 4297
48. M. Suresh, A.K. Mandal, S. Saha, E. Suresh, A. Mandoli, R.D. Liddo, P.P. Parnigotto, and A. Das Org. Lett. 12 2010 5406 5409
49. K.S. Jain, T.S. Chitre, P.B. Miniyar, M.K. Kathiravan, V.S. Bendre, V.S. Veer, S.R. Shahane, and C.J. Shishoo Curr. Sci. 90 2006 793 803
50. K.T. Wong, T.S. Hung, Y. Lin, C.C. Wu, G.H. Lee, S.M. Peng, C.H. Chou, and Y.O. Su Org. Lett. 4 2002 513 516
51. C.C. Wu, Y.T. Lin, H.H. Chiang, T.Y. Cho, and C.W. Chen Appl. Phys. Lett. 81 2002 577 579
52. G. Hughes, C. Wang, A.S. Batsanov, M. Fern, S. Frank, M.R. Bryce, I.F. Perepichka, A.P. Monkman, and B.P. Lyons Org. Biomol. Chem. 1 2003 3069 3077
53. C.F. Lin, W.S. Huang, H.H. Chou, and J.T. Lin J. Organomet. Chem. 694 2009 2757 2769
54. G. Ge, J. He, H. Guo, F. Wang, and D. Zou J. Organomet. Chem. 694 2009 3050 3057
55. Z.Q. Wang, C. Xu, X.M. Dong, Y.P. Zhang, X.Q. Hao, J.F. Gong, M.P. Song, and B.M. Ji Inorg. Chem. Commun. 14 2011 316 319
56. S.J. Su, C. Cai, and J. Kido Chem. Mater. 23 2011 274 284
57. T. Sasada, F. Kobayashi, N. Sakai, and T. Konakahara Org. Lett. 11 2009 2161 2164
58. J.A. Simon, S.L. Curry, R.H. Schmehl, T.R. Schatz, P. Piotrowiak, X. Jin, and R.P. Thummel J. Am. Chem. Soc. 119 1997 11012 11022
59. M. Shortreed, R. Kopelman, M. Kuhn, and B. Hoyland Anal. Chem. 68 1996 1414 1418
60. E.M. Nolan, M.E. Racine, and S.J. Lippard Inorg. Chem. 45 2006 2742 2749
61. S. Hamai, and F. Hirayama J. Phys. Chem. 87 1983 83 89