8-TQEN (N,N,N′,N′-tetrakis(8-quinolylmethyl)ethylenediamine) analogs as fluorescent cadmium sensors: Strategies to enhance Cd 2+-induced fluorescence and Cd2+/Zn2+ selectivity

RSC Advances

Volumn 4, Issue 25, 2014, Pages 12849-12856

  Mikata, Yuji ^a   Takekoshi, Ayaka ^a   Kizu, Asako ^a   Nodomi, Yuki ^a   Aoyama, Masato ^a   Yasuda, Keiko ^a   Tamotsu, Satoshi ^a   Konno, Hideo ^b   Burdette, Shawn C ^c  

^a NARA WOMEN'S UNIVERSITY   (Japan)

^b NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY AIST   (Japan)

^c Life Science and Bioengineering Center   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

8-HYDROXYQUINOLINE; AQUEOUS MEDIA; ETHYLENE DIAMINE; FLUORESCENCE ENHANCEMENT; FLUORESCENT PROBES; POOR SOLUBILITIES; QUINOLINE GROUPS; SELECTIVE FLUORESCENCE;

FLUORESCENCE; ZINC;

CADMIUM COMPOUNDS;

EID: 84896740781     PISSN: None     EISSN: 20462069     Source Type: Journal    
DOI: 10.1039/c4ra00010b     Document Type: Article

References (31)

1. A. P. de Silva H. Q. N. Gunaratne T. Gunnlaugsson A. J. M. Huxley C. P. McCoy J. T. Rademacher T. E. Rice Chem. Rev. 1997 97 1515 1566
2. A. P. de Silva D. B. Fox A. J. M. Huxley N. D. McClenaghan J. Roiron Coord. Chem. Rev. 1999 185-186 297 306
3. E. L. Que D. W. Domaille C. J. Chang Chem. Rev. 2008 108 1517 1549
4. L. M. Hyman K. J. Franz Coord. Chem. Rev. 2012 256 2333 2356
5. Z. Liu W. He Z. Guo Chem. Soc. Rev. 2013 42 1568 1600
6. R. D. Hancock Chem. Soc. Rev. 2013 42 1500 1524
7. B. Valeur I. Leray Coord. Chem. Rev. 2000 205 3 40
8. C. J. Frederickson E. J. Kasarskis D. Ringo R. E. Frederickson J. Neurosci. Methods 1987 20 91 103
9. M. S. Nasir C. J. Fahrni D. A. Suhy K. J. Kolodsick C. P. Singer T. V. O'Halloran J. Bioinorg. Chem. 1999 4 775 783
10. C. J. Fahrni T. V. O'Halloran J. Am. Chem. Soc. 1999 121 11448 11458
11. E. Tomat S. J. Lippard Curr. Opin. Chem. Biol. 2010 14 225 230
12. X. Peng J. Du J. Fan J. Wang Y. Wu J. Zhao S. Sun T. Xu J. Am. Chem. Soc. 2007 129 1500 1501
13. T. Cheng Y. Xu S. Zhang W. Zhu X. Qian L. Duan J. Am. Chem. Soc. 2008 130 16160 16161
14. X.-L. Tang X.-H. Peng W. Dou J. Mao J.-R. Zheng W.-W. Qin W.-S. Liu J. Chang X.-J. Yao Org. Lett. 2008 10 3653 3656
15. Z. Li P. Xi L. Huang G. Xie Y. Shi H. Liu M. Xu F. Chen Z. Zeng Inorg. Chem. Commun. 2011 14 1241 1244
16. L. Xue G. Li Q. Liu H. Wang X. Liu C. Ding S. He H. Jiang Inorg. Chem. 2011 50 3680 3690
17. S. Goswami K. Aich S. Das A. K. Das A. Manna S. Halder Analyst 2013 138 1903 1907
18. A. M. Costero S. Gil J. Sanchis S. Peransí V. Sanz J. A. G. Williams Tetrahedron 2004 60 6327 6334
19. C. Lu Z. Xu J. Cui R. Zhang X. Qian J. Org. Chem. 2007 72 3554 3557
20. X. Zhou P. Li Z. Shi X. Tang C. Chen W. Liu Inorg. Chem. 2012 51 9226 9231
21. Y. Mikata Y. Sato S. Takeuchi Y. Kuroda H. Konno S. Iwatsuki Dalton Trans. 2013 42 9688 9698
22. Y. Mikata Y. Nodomi A. Kizu H. Konno Dalton Trans. 2014 43 1684 1690
23. Y. Mikata M. Wakamatsu S. Yano Dalton Trans. 2005 545 550
24. Y. Mikata M. Wakamatsu A. Kawamura N. Yamanaka S. Yano A. Odani K. Morihiro S. Tamotsu Inorg. Chem. 2006 45 9262 9268
25. Y. Mikata A. Yamanaka A. Yamashita S. Yano Inorg. Chem. 2008 47 7295 7301
26. Y. Mikata K. Kawata S. Iwatsuki H. Konno Inorg. Chem. 2012 51 1859 1865
27. G. Weber J. Riecke W. Saenger G. M. Sheldrick Inorg. Chim. Acta 1981 54 L185 L186
28. R. Bartzatt L. Donigan Lett. Drug Des. Discovery 2004 1 78 83
29. Y. Sakurai M. Izumi Pharm. Bull. 1953 1 297 301
30. K. Schlögl R. Schlögl Monatsh. Chem. 1964 95 922 941
31. W. Gan S. B. Jones J. H. Reibenspies R. D. Hancock Inorg. Chim. Acta 2005 358 3958 3966