Copyright (c) 2015 AJC
This work is licensed under a Creative Commons Attribution 4.0 International License.
Study on Fluorescence Properties of Boradiazaindacenes (BODIPY) in Different Surfactant Solutions
Corresponding Author(s) : Yongjun Lv
Asian Journal of Chemistry,
Vol. 27 No. 5 (2015): Vol 27 Issue 5
Abstract
A novel yellow-green fluorescent BODIPY dye (1) was synthesized and its fluorescence properties were investigated in various surfactant solutions, including myristyltrimethylammonium bromide, sodium dodecylbenzenesulphonate, sodium dodecylsulfate and triton X-100. The results show that BODIPY dye (1) displays an obvious fluorescence sensitizing effect in the presence of myristyltrimethylammonium bromide, which can be attributed to the entrance of 1 into myristyltrimethylammonium bromide micelle. Furthermore, there is a good linear relationship between fluorescence intensity and myristyltrimethylammonium bromide concentration in the range of 0-2.1 × 10-3 mol/L, with the association constant of 3.71 × 104.
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- K.P. Carter, A.M. Young and A.E. Palmer, Chem. Rev., 114, 4564 (2014); doi:10.1021/cr400546e.
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References
K.P. Carter, A.M. Young and A.E. Palmer, Chem. Rev., 114, 4564 (2014); doi:10.1021/cr400546e.
D. Sareen, P. Kaur and K. Singh, Coord. Chem. Rev., 265, 125 (2014); doi:10.1016/j.ccr.2014.01.015.
L.M. Hyman and K.J. Franz, Coord. Chem. Rev., 256, 2333 (2012); doi:10.1016/j.ccr.2012.03.009.
P.M. Schäferling, Angew. Chem. Int. Ed., 51, 3532 (2012); doi:10.1002/anie.201105459.
G. Ulrich, R. Ziessel and A. Harriman, Angew. Chem. Int. Ed., 47, 1184 (2008); doi:10.1002/anie.200702070.
A. Loudet and K. Burgess, Chem. Rev., 107, 4891 (2007); doi:10.1021/cr078381n.
R. Yoshii, H. Yamane, A. Nagai, K. Tanaka, H. Taka, H. Kita and Y. Chujo, Macromolecules, 47, 2316 (2014); doi:10.1021/ma5002047.
S. Zhu, J. Zhang, J. Janjanam, G. Vegesna, F.T. Luo, A. Tiwari and H. Liu, J. Mater. Chem. B, 1, 1722 (2013); doi:10.1039/c3tb00249g.
T. Bura and R. Ziessel, Org. Lett., 13, 3072 (2011); doi:10.1021/ol200969r.
K. Peneva, G. Mihov, F. Nolde, S. Rocha, J.- Hotta, K. Braeckmans, J. Hofkens, H. Uji-i, A. Herrmann and K. Müllen, Angew. Chem. Int. Ed., 47, 3372 (2008); doi:10.1002/anie.200705409.
M.V. Reddington, Bioconjug. Chem., 18, 2178 (2007); doi:10.1021/bc070090y.
H. Wang, Z. Lu, S.J. Lord, W.E. Moerner and R.J. Twieg, Tetrahedron Lett., 48, 3471 (2007); doi:10.1016/j.tetlet.2007.03.026.
N.R. Jie, W.Y. Ling, H. Yu and Y. Cheng, Asian J. Chem., 24, 5011 (2012).
C. Bombelli, G. Caracciolo, P. Di Profio, M. Diociaiuti, P. Luciani, G. Mancini, C. Mazzuca, M. Marra, A. Molinari, D. Monti, L. Toccacieli and M. Venanzi, J. Med. Chem., 48, 4882 (2005); doi:10.1021/jm050182d.
E.H. Hill, H.C. Pappas and D.G. Whitten, Langmuir, 30, 5052 (2014); doi:10.1021/la501230m.
J.J. Morelli and G. Szajer, J. Surfactants Deterg., 4, 75 (2001); doi:10.1007/s11743-001-0163-7.
Y.H. Liu, H.W. Zhan and W.X. Ma, Asian J. Chem., 25, 2736 (2013); doi:10.14233/ajchem.2013.13761.
M. Kollmannsberger, K. Rurack, U. Resch-Genger and J. Daub, J. Phys. Chem. A, 102, 10211 (1998); doi:10.1021/jp982701c.
K. Rurack, M. Kollmannsberger and J. Daub, Angew. Chem. Int. Ed., 40, 385 (2001); doi:10.1002/1521-3773(20010119)40:2<385::AID-ANIE385>3.0.CO;2-F.
A. Rauf, W. Rehman, M. Amanullah, A. Khan and M. Akram, Asian J. Chem., 25, 559 (2013); doi:10.14233/ajchem.2013.13599.
H. Topallar and B. Karadag, J. Surfactants Deterg., 1, 49 (1998); doi:10.1007/s11743-998-0007-5.