Fluorescence enhancement of N 2O 2-type dipyrrin ligand in two step responding to zinc(II) ion

Journal of Luminescence

Volumn 132, Issue 11, 2012, Pages 3089-3092

  Song, Hyesun ^a   Rajendiran, Senkuttuvan ^a   Koo, Eunhae ^b   Min, Byoung Koun ^c   Jeong, Soon Kwan ^d   Daniel Thangadurai, T ^a   Yoon, Sungho ^a  

^a Kookmin University   (South Korea)

^b Korea Institute of Ceramic Engineering and Technology (KICET)   (South Korea)

^c Hydrogen Energy Research Center   (South Korea)

^d Korea Institute of Energy Research (KIER)   (South Korea)

Author keywords

Detection limit; Dipyrrin; Fluorescence enhancement; Ligand complex; Zinc(II)

Indexed keywords

BINDING AFFINITIES; BLUE-SHIFTED; CHLORO COMPLEXES; DETECTION LIMITS; DIPYRRIN; EMISSION INTENSITY; ENHANCED FLUORESCENCE EMISSION; EXCITED-STATE DYNAMICS; FLUORESCENCE EMISSION; FLUORESCENCE ENHANCEMENT; FLUORESCENCE IMAGING; FLUORESCENCE PROPERTIES; FLUORESCENCE TITRATIONS; HIGH SENSITIVITY; IMAGING AGENT; IN-VIVO; LIGAND COMPLEXES; MAGNETIC SIGNATURES; MICROMOLAR CONCENTRATION; NAKED-EYE; TEMPORAL FIDELITY; ZINC COMPLEX;

BINDING ENERGY; COMPLEXATION; FLUORESCENCE; ZINC;

ZINC COMPOUNDS;

EID: 84864026414     PISSN: 00222313     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jlumin.2012.06.024     Document Type: Article

References (29)

1. L. Bonardi, H. Kanaan, F. Camerel, P. Jolinat, P. Retailleau, and R. Ziessel Adv. Funct. Mater. 18 2008 401
2. I.V. Sazanovich, C. Kirmaier, E. Hindin, L. Yu, D.F. Bocian, J.S. Lindsey, and D. Holten J. Am. Chem. Soc. 126 2004 2664
3. V.S. Thoi, J.R. Stork, D. Magde, and S.M. Cohen Inorg. Chem. 45 2006 10688
4. G. Ulrich, R. Ziessel, and A. Harriman Angew. Chem. Int. Ed. 47 2008 1184
5. C. Bronner, S.A. Baudron, M.W. Hosseini, C.A. Strassert, A. Guenet, and L.D. Cola Dalton Trans. 39 2010 180
6. T.E. Wood, N.D. Dalgleish, E.D. Power, A. Thompson, X. Chen, and Y. Okamoto J. Am. Chem. Soc. 127 2005 5740
7. H.G. Lee, J.H. Lee, S.P. Jang, H.M. Park, S.J. Kim, Y. Kim, C. Kim, and R.G. Harrison Tetrahedron 67 2011 8073
8. C.J. Chang, E.M. Nolan, J. Jaworski, K.I. Okamoto, Y. Hayashi, M. Sheng, and S.J. Lippard Inorg. Chem. 43 2004 6774
9. E.M. Nolan, and S.J. Lippard Acc. Chem. Res. 42 2009 193
10. M. Taki, J.L. Wolford, and T.V. O'Halloran J. Am. Chem. Soc. 126 2004 712
11. H.M. Kim, and B.R. Cho Acc. Chem. Res. 42 2009 863
12. A.R. Morales, and C.O. Yanez Bioconjugate Chem. 20 2009 1992
13. For a recent review see Z.C. Xu, J. Yoon, and D.R. Spring Chem. Soc. Rev. 39 2010 1996
14. S.A. Baudron Cryst. Eng. Commun. 12 2010 2288
15. C. Bronner, M. Veiga, A. Guenet, L. De Cola, M. Wais Hosseini, C.A. Strassert, and S.A. Baudron Chem. Eur. J. 18 2012 4041
16. C. Ikeda, S. Ueda, and T. Nabeshima Chem. Commun. 2009 2544
17. H. Maeda, T. Hashimoto, R. Fujii, and M. Hasegawa J. Nanosci. Nanotechnol. 9 2009 240
18. M.A. Filatov, A.Y. Lebedev, S.N. Mukhin, S.A. Vinogradov, and A.V. Cheprakov J. Am. Chem. Soc. 132 2010 9552
19. L. Yu, K. Muthukumaran, I.V. Sazanovich, C. Kirmaier, E. Hindin, J.R. Diers, P.D. Boyle, D.F. Bocian, D. Holten, and J.S. Lindsey Inorg. Chem. 42 2003 6629
20. R.W. Wagner, and J.S. Lindsey Pure Appl. Chem. 68 1996 1373
21. Á. Álvarez, R. Macías, M.J. Fabra, M.L. Martín, F.J. Lahoz, and L.A. Oro Inorg. Chem. 46 2007 6811
22. H. Jiang, and D. Song Organometallics 27 2008 3587
23. S.C. Zinner, W.A. Herrmann, and F.E. Kühn J. Organomet. Chem. 693 2008 1543
24. 13C NMR Values were Slightly Different than Previously Reported.
25. 2 to BB2 (Supplementary data).
26. D.W. Domaille, E.L. Que, and C.J. Chang Nat. Chem. Biol. 4 2008 168
27. E.M. Nolan, J. Jaworski, K.I. Okamoto, Y. Hayashi, M. Sheng, and S.J. Lippard J. Am. Chem. Soc. 127 2005 16812
28. M.N. Dao, W. Xuhua, A. Hyo-Yang, R. Luis, V.B. Mikhailo, and D.B. Kevin Appl. Mater. Interfaces. 2 2010 2978
29. J. Kajally, H.B. Caroline, M. Majid, M.G. Stephen, and M. Watkinson Chem. Commun. 47 2011 6036