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Synthesis and Structural Characterizations of meso-Tetraphenyl Porphyrin
Corresponding Author(s) : Jianbin Zhang
Asian Journal of Chemistry,
Vol. 26 No. 10 (2014): Vol 26 Issue 10
Abstract
In this paper, tetraphenyl porphyrin (H2TPP) was synthesized by using pyrrole and benzaldehyde as raw materials under the catalysis of p-nitrobenzoic acid. The prepared tetraphenyl porphyrin was re-crystallized in a mixed system of methanol and methylene chloride (CH2Cl2) and the yield of tetraphenyl porphyrin is 34.2 %. Tetraphenyl porphyrin was characterized by using FTIR, UV-visible, 1H NMR and fluorescence spectrophotometer. The effects on the yield of tetraphenyl porphyrin at different volumes of dimethylbenzene as solvent were explored.
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- A.R. Battersby, C.J.R. Fookes, G.W.J. Matcham and E. McDonald, Nature, 285, 17 (1980); doi:10.1038/285017a0.
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- J. Yu, J.W. Meng, Y. Li, J. Ma and R.E. Zheng, Spectrosc. Spect. Anal., 8, 981 (2004).
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- L.Z. Wang and Y.B. She, Spectrosc. Spect. Anal., 28, 2312 (2008).
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References
A.R. Battersby, C.J.R. Fookes, G.W.J. Matcham and E. McDonald, Nature, 285, 17 (1980); doi:10.1038/285017a0.
R. Shoji, T. Takeuchi and I. Kubo, Anal. Chem., 75, 4882 (2003); doi:10.1021/ac020795n.
J.B. Zhang, P.Y. Zhang, G.H. Chen, F. Han and X.H. Wei, Prog. Chem., 4, 771 (2009).
Y. Zhang, Chem. Petrol. Eng., 7, 114 (2010).
L.J. Boucher and J.J. Katz, J. Am. Chem. Soc., 89, 4703 (1967); doi:10.1021/ja00994a024.
A. Kumar, S. Maji, P. Dubey, G.J. Abhilash, S. Pandey and S. Sarkar, Tetrahedron Lett., 48, 7287 (2007); doi:10.1016/j.tetlet.2007.08.046.
R. Lucas, J. Vergnaud, K. Teste, R. Zerrouki, V. Sol and P. Krausz, Tetrahedron Lett., 49, 5537 (2008); doi:10.1016/j.tetlet.2008.07.058.
C.C. Guo, X.T. He and G.Y. Zhou, Chinese J. Org. Chem., 4, 416 (1991).
S. Xiao, J. Guiyang Med. Univ., 30, 49 (2005).
D.Q. An and D.Z. Yang, Spectrosc. Spect. Anal., 4, 478 (2001).
J. Yu, J.W. Meng, Y. Li, J. Ma and R.E. Zheng, Spectrosc. Spect. Anal., 8, 981 (2004).
M. Lan, H.G. Zhao, H.H. Yuan, C. Jiang, S. Zuo and Y. Jiang, Dyes Pigments, 74, 357 (2007); doi:10.1016/j.dyepig.2006.02.018.
L.Z. Wang and Y.B. She, Spectrosc. Spect. Anal., 28, 2312 (2008).
H. Dehghani and F. Fathi, Dyes Pigments, 77, 323 (2008); doi:10.1016/j.dyepig.2007.05.017.
H. Chiniforoshan, N. Safari, J.M. Nezhad, H. Hadadzadeh and A.H. Mahmoudkhani, Inorg. Chim. Acta, 359, 2101 (2006); doi:10.1016/j.ica.2006.01.015.