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Synthesis, Optical Properties and Morphology of Film of Novel Bridged Double Benzimidazole Perylene Derivative
Corresponding Author(s) : Hai-Quan Zhang
Asian Journal of Chemistry,
Vol. 27 No. 11 (2015): Vol 27 Issue 11
Abstract
A bridged double benzimidazole perylene derivative (BIDP) was synthesized from 3,4,9,10-perylenetetracarboxylic dianhydride. UV-visible spectrum and fluorescence spectrum of BIDP were studied in DMF, which showed that the maximum absorption peak was at 525 nm and the other characteristic absorption peaks were at 498 and 566 nm and the emission peak was at 540 and 580 nm. Then the film of BIDP was made by the electrodeposition. The optical physical properties, morphology and aggregation structure were investigated by UV-visible and fluorescence spectra. The characterization were investigated by UV-visible, fluorescence spectrum, SEM and XRD. Finally, the electrodeposition films that had ordered morphology were got by DMF vapour annealing.
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- C.W. Tang, Appl. Phys. Lett., 48, 183 (1986); doi:10.1063/1.96937.
- B.A. Jones, A. Facchetti, M.R. Wasielewski and T.J. Marks, J. Am. Chem. Soc., 129, 15259 (2007); doi:10.1021/ja075242e.
- B.A. Jones, A. Facchetti, T.J. Marks and M.R. Wasielewski, Chem. Mater., 19, 2703 (2007); doi:10.1021/cm0704579.
- K.C. See, C. Landis, A. Sarjeant and H.E. Katz, Chem. Mater., 20, 3609 (2008); doi:10.1021/cm7032614.
- Y. Che, A. Datar, K. Balakrishnan and L. Zang, J. Am. Chem. Soc., 129, 7234 (2007); doi:10.1021/ja071903w.
- M. Adachi, Y. Murata and S. Nakamura, J. Phys. Chem., 99, 14240 (1995); doi:10.1021/j100039a009.
- S.L. Oliveira, B.S. Correa, L. Misoguti, C.J.L. Constantino, R.F. Aroca, S.C. Zilio and C.R. Mendonça, Adv. Mater., 17, 1890 (2005); doi:10.1002/adma.200500533.
- G. Horowitz, F. Kouki, P. Spearman, D. Fichou, C. Nogues, X. Pan and F. Garnier, Adv. Mater., 8, 242 (1996); doi:10.1002/adma.19960080312.
- H.G. Löhmannsröben and H. Langhals, Appl. Phys. B, 48, 449 (1989); doi:10.1007/BF00694678.
- W. Wang, J.J. Han, L.Q. Wang, L.S. Li, W.J. Shaw and A.D.Q. Li, Nano Lett., 3, 455 (2003); doi:10.1021/nl025976j.
- S.H. Oh, B.G. Kim, S.J. Yun, M. Maheswara, K. Kim and J.Y. Do, Dyes Pigments, 85, 37 (2010); doi:10.1016/j.dyepig.2009.10.001.
- R.O. Marcon and S. Brochsztain, J. Phys. Chem., 113, 1747 (2009); doi:10.1021/jp808383e.
References
C.W. Tang, Appl. Phys. Lett., 48, 183 (1986); doi:10.1063/1.96937.
B.A. Jones, A. Facchetti, M.R. Wasielewski and T.J. Marks, J. Am. Chem. Soc., 129, 15259 (2007); doi:10.1021/ja075242e.
B.A. Jones, A. Facchetti, T.J. Marks and M.R. Wasielewski, Chem. Mater., 19, 2703 (2007); doi:10.1021/cm0704579.
K.C. See, C. Landis, A. Sarjeant and H.E. Katz, Chem. Mater., 20, 3609 (2008); doi:10.1021/cm7032614.
Y. Che, A. Datar, K. Balakrishnan and L. Zang, J. Am. Chem. Soc., 129, 7234 (2007); doi:10.1021/ja071903w.
M. Adachi, Y. Murata and S. Nakamura, J. Phys. Chem., 99, 14240 (1995); doi:10.1021/j100039a009.
S.L. Oliveira, B.S. Correa, L. Misoguti, C.J.L. Constantino, R.F. Aroca, S.C. Zilio and C.R. Mendonça, Adv. Mater., 17, 1890 (2005); doi:10.1002/adma.200500533.
G. Horowitz, F. Kouki, P. Spearman, D. Fichou, C. Nogues, X. Pan and F. Garnier, Adv. Mater., 8, 242 (1996); doi:10.1002/adma.19960080312.
H.G. Löhmannsröben and H. Langhals, Appl. Phys. B, 48, 449 (1989); doi:10.1007/BF00694678.
W. Wang, J.J. Han, L.Q. Wang, L.S. Li, W.J. Shaw and A.D.Q. Li, Nano Lett., 3, 455 (2003); doi:10.1021/nl025976j.
S.H. Oh, B.G. Kim, S.J. Yun, M. Maheswara, K. Kim and J.Y. Do, Dyes Pigments, 85, 37 (2010); doi:10.1016/j.dyepig.2009.10.001.
R.O. Marcon and S. Brochsztain, J. Phys. Chem., 113, 1747 (2009); doi:10.1021/jp808383e.