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Study of Electronic Absorption Spectra of Thiophene Schiff Bases in Varied pH Buffer Solutions
Corresponding Author(s) : M. El-Batouti
Asian Journal of Chemistry,
Vol. 27 No. 11 (2015): Vol 27 Issue 11
Abstract
The absorption spectrum was measured for Schiff bases of thiophene in buffer solution at 25 °C to study medium effect in acidic and basic solutions, to determine pKa values and to identify the sensitivity of these compounds for the ionization movement in the medium. This facilitates the studied process of these compounds and understanding of their behaviour when exposed to electron acceptors. The UV-visible spectra of the Schiff bases were studied in buffer solutions of different pH = (2-12) containing 30 % (v/v) ethanol to affect the solubility of the organic compounds. In the present paper the electronic absorption spectra of some Schiff base compounds derived from thiophene have studied in organic solvents of varying polarity and buffer solutions of different pH.
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- E.M. Nour, S.M. Metwally, M.A.F. El-Mosallamy and Y. Gameel, Spectrosc. Lett.,30, 1109 (1997); doi:10.1080/00387019708006710.
- R. Foster, Organic Charge-Transfer Complexes, Academic Press, London and New York (1969).
- R. Foster and T.J. Thomson, Trans. Faraday Soc., 58, 860 (1962); doi:10.1039/tf9625800860.
- R.S. Mulliken and W.B. Person, Molecular Complexes, A Lecture and Reprint Volume, Wiley, New York (1969).
- S.M. Metwally, Can. J. Appl. Spectrosc., 40, 152 (1995).
- K.K. Lahiri, K.K. Mazumdar and K. Masumdar, Spectrochim. Acta A, 46, 1137 (1990); doi:10.1016/0584-8539(90)80231-M.
- L.I. Bebawy, K.E. Kelani, L.A. Fattah and A.K.S. Ahmad, J. Pharm. Sci., 86, 1030 (1997); doi:10.1021/js960504o.
- M. Luo, Yaowu Fenxi Zazhi, 15, 52 (1995).
- E.H. El-Mossalamy and K.Y. El-Baradie, Monatsh. Chem., 128, 255 (1997);doi:10.1007/BF00807891.
- J. Czekalla, G. Briegleb and W. Herre, Ber. Bunsenges. Phys. Chem., 63, 712 (1959); doi:10.1002/bbpc.19590630612.
- G. Briegleb, Angew. Chem., 76, 326 (1964); doi:10.1002/ange.19640760804.
- R. Foster, D.L. Hammick and B.N. Parsons, J. Chem. Soc., 555 (1956); doi:10.1039/jr9560000555.
- Y.M. Issa, A.E. El-kholy, A.M. Hindawy and R.M. Issa, J. Indian Chem. Soc., 57, 216 (1980).
- R.M. Issa, A.A. El-Samahy and S.H. Etaiw, Z. Phys. Chem. (Leipz.), 253, 853 (1974).
- H.T.S. Britton, Hydrogen Ions , Chapman and Hall, London (1955).
- S.A. Abdel-Latif, H.B. Hassib and Y.M. Issa, Spectrochim. Acta A, 67, 950 (2007); doi:10.1016/j.saa.2006.09.013.
- R.M. Issa, A.A. Hassanein, I.M. El-Mehasseb and R.I.A. El-Wadoud, Spectrochim. Acta A, 65, 206 (2006); doi:10.1016/j.saa.2005.10.032.
- T. Sakabe, M. Iizuka, S. Kuniyoshi, K. Kudo and K. Tanaka, Mol. Cryst. Liq. Cryst., 349, 367 (2000); doi:10.1080/10587250008024940.
- K. Kudo, M. Iizuka, S. Kuniyoshi and K. Tanaka, Electr. Eng. Jpn., 134, 10 (2001); doi:10.1002/1520-6416(20010115)134:1<10::AID-EEJ2>3.0.CO;2-D.
- R.M. Issa and A.H. Zewail, Egypt. J. Chem., 14, 461 (1971).
- I.M. Issa, R.M. Issa, M.S. El-Ezaby and Y.Z. Ahmed, Z. Phys. Chem. (Leipzig), 242, 169 (1969).
- A. Harvey and D. Manning, J. Am. Chem. Soc., 72, 4488 (1950); doi:10.1021/ja01166a044.
- R.M. Issa, K.Y. El-baradie and N.A. El-Wakiel, Spectrochim. Acta A, 60, 2883 (2004); doi:10.1016/j.saa.2004.01.023.
- A.M. Khedr, M. Gaber, R.M. Issa and H. Erten, Dyes Pigments, 67, 117 (2005); doi:10.1016/j.dyepig.2004.11.004.
- R.M. Issa, A.M. Khedr and H. Rizk, J. Chil. Chem. Soc., 55, 875 (2008).
References
E.M. Nour, S.M. Metwally, M.A.F. El-Mosallamy and Y. Gameel, Spectrosc. Lett.,30, 1109 (1997); doi:10.1080/00387019708006710.
R. Foster, Organic Charge-Transfer Complexes, Academic Press, London and New York (1969).
R. Foster and T.J. Thomson, Trans. Faraday Soc., 58, 860 (1962); doi:10.1039/tf9625800860.
R.S. Mulliken and W.B. Person, Molecular Complexes, A Lecture and Reprint Volume, Wiley, New York (1969).
S.M. Metwally, Can. J. Appl. Spectrosc., 40, 152 (1995).
K.K. Lahiri, K.K. Mazumdar and K. Masumdar, Spectrochim. Acta A, 46, 1137 (1990); doi:10.1016/0584-8539(90)80231-M.
L.I. Bebawy, K.E. Kelani, L.A. Fattah and A.K.S. Ahmad, J. Pharm. Sci., 86, 1030 (1997); doi:10.1021/js960504o.
M. Luo, Yaowu Fenxi Zazhi, 15, 52 (1995).
E.H. El-Mossalamy and K.Y. El-Baradie, Monatsh. Chem., 128, 255 (1997);doi:10.1007/BF00807891.
J. Czekalla, G. Briegleb and W. Herre, Ber. Bunsenges. Phys. Chem., 63, 712 (1959); doi:10.1002/bbpc.19590630612.
G. Briegleb, Angew. Chem., 76, 326 (1964); doi:10.1002/ange.19640760804.
R. Foster, D.L. Hammick and B.N. Parsons, J. Chem. Soc., 555 (1956); doi:10.1039/jr9560000555.
Y.M. Issa, A.E. El-kholy, A.M. Hindawy and R.M. Issa, J. Indian Chem. Soc., 57, 216 (1980).
R.M. Issa, A.A. El-Samahy and S.H. Etaiw, Z. Phys. Chem. (Leipz.), 253, 853 (1974).
H.T.S. Britton, Hydrogen Ions , Chapman and Hall, London (1955).
S.A. Abdel-Latif, H.B. Hassib and Y.M. Issa, Spectrochim. Acta A, 67, 950 (2007); doi:10.1016/j.saa.2006.09.013.
R.M. Issa, A.A. Hassanein, I.M. El-Mehasseb and R.I.A. El-Wadoud, Spectrochim. Acta A, 65, 206 (2006); doi:10.1016/j.saa.2005.10.032.
T. Sakabe, M. Iizuka, S. Kuniyoshi, K. Kudo and K. Tanaka, Mol. Cryst. Liq. Cryst., 349, 367 (2000); doi:10.1080/10587250008024940.
K. Kudo, M. Iizuka, S. Kuniyoshi and K. Tanaka, Electr. Eng. Jpn., 134, 10 (2001); doi:10.1002/1520-6416(20010115)134:1<10::AID-EEJ2>3.0.CO;2-D.
R.M. Issa and A.H. Zewail, Egypt. J. Chem., 14, 461 (1971).
I.M. Issa, R.M. Issa, M.S. El-Ezaby and Y.Z. Ahmed, Z. Phys. Chem. (Leipzig), 242, 169 (1969).
A. Harvey and D. Manning, J. Am. Chem. Soc., 72, 4488 (1950); doi:10.1021/ja01166a044.
R.M. Issa, K.Y. El-baradie and N.A. El-Wakiel, Spectrochim. Acta A, 60, 2883 (2004); doi:10.1016/j.saa.2004.01.023.
A.M. Khedr, M. Gaber, R.M. Issa and H. Erten, Dyes Pigments, 67, 117 (2005); doi:10.1016/j.dyepig.2004.11.004.
R.M. Issa, A.M. Khedr and H. Rizk, J. Chil. Chem. Soc., 55, 875 (2008).