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Synthesis, Spectroscopic Characterization and Thermal Studies of (E,E)-2-Hydroxy-3-methoxybenzaldehyde Azine
Corresponding Author(s) : Guangquan Mei
Asian Journal of Chemistry,
Vol. 26 No. 4 (2014): Vol 26 Issue 4
Abstract
Hydrazone, (E,E)-2-hydroxy-3-methoxybenzaldehyde azine was synthesized and its spectroscopic characterization was studied via IR, 1H NMR, MS and XRD. Its fluorescence activity and thermal stability were also analyzed.
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- M.S. Refat and A.A. Ibrahim, Spectrochim. Acta A, 70, 234 (2008); doi:10.1016/j.saa.2007.05.065.
- D.F. Taber and P.F. Guo, J. Org. Chem., 73, 9479 (2008); doi:10.1021/jo8017704.
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- S.P. Douglas and P.N. Rao, Int. J. Eng. Sci. Technol., 2, 4655 (2010).
- N.H. Al-Sha’alan, Molecules, 12, 1080 (2007); doi:10.3390/12051080.
- S.K. Sridhar, M. Saravanan and A. Ramesh, Eur. J. Med. Chem., 36, 615 (2001); doi:10.1016/S0223-5234(01)01255-7.
- V. Alptüzün, S. Parlar, H. Tasli and E. Erciyas, Molecules, 14, 5203 (2009); doi:10.3390/molecules14125203.
- C. Mirela, I. Emilia and G. Rodica, Rev. Roum. Chim., 10, 911 (2008).
- S.N. Pandeya, A.S.Raja and J.P.Stables, J. Pharm. Pharmaceut. Sci., 3, 266 (2002).
- C.M. Moldovan, O. Oniga, A. Pârvu, B. Tiperciuc, P. Verite, A. Pîrnău, O. Crişan, M. Bojiţă and R. Pop, Eur. J. Med. Chem., 46, 526 (2011); doi:10.1016/j.ejmech.2010.11.032.
- S. Gemma, G. Kukreja, C. Fattorusso, M. Persico, M.P. Romano, M. Altarelli, L. Savini, G. Campiani, E. Fattorusso, N. Basilico, D. Taramelli, V. Yardley and S. Butini, Bioorg. Med. Chem. Lett., 16, 5384 (2006); doi:10.1016/j.bmcl.2006.07.060.
- A. Nayyar, A. Malde, E. Coutinho and R. Jain, Bioorg. Med. Chem., 14, 7302 (2006); doi:10.1016/j.bmc.2006.06.049.
- M.K. Mao and J.E. Franz, Synthesis, 920 (1991); doi:10.1055/s-1991-26606.
- M. Böger, D. Dürr, L. Gsell, R. G Hall, F. Karrer, O. Kristiansen, P. Maienfisch, A. Pascual and A. Rindlisbacher, Pest Manag. Sci., 57, 191 (2001) doi:10.1002/1526-4998(200102)57:2<191::AID-PS275>3.0.CO;2-O.
- J.B. Raoof, R. Ojani and Z. Mohammadpour, Int. J. Electrochem. Soc., 5, 177 (2010).
References
M.S. Refat and A.A. Ibrahim, Spectrochim. Acta A, 70, 234 (2008); doi:10.1016/j.saa.2007.05.065.
D.F. Taber and P.F. Guo, J. Org. Chem., 73, 9479 (2008); doi:10.1021/jo8017704.
J. Chakraborty, R.K.B. Singh, B. Samanta, C.R. Choudhury, S.K. Dey, P. Talukder, M.J. Borah and S. Mitra, Z. Naturforsch., 61b, 1209 (2006).
A. Irshad, K. Misbah-ul-Ain and A. Makshoof, J. Pure Appl.Sci., 17, 67 (1998).
S.P. Douglas and P.N. Rao, Int. J. Eng. Sci. Technol., 2, 4655 (2010).
N.H. Al-Sha’alan, Molecules, 12, 1080 (2007); doi:10.3390/12051080.
S.K. Sridhar, M. Saravanan and A. Ramesh, Eur. J. Med. Chem., 36, 615 (2001); doi:10.1016/S0223-5234(01)01255-7.
V. Alptüzün, S. Parlar, H. Tasli and E. Erciyas, Molecules, 14, 5203 (2009); doi:10.3390/molecules14125203.
C. Mirela, I. Emilia and G. Rodica, Rev. Roum. Chim., 10, 911 (2008).
S.N. Pandeya, A.S.Raja and J.P.Stables, J. Pharm. Pharmaceut. Sci., 3, 266 (2002).
C.M. Moldovan, O. Oniga, A. Pârvu, B. Tiperciuc, P. Verite, A. Pîrnău, O. Crişan, M. Bojiţă and R. Pop, Eur. J. Med. Chem., 46, 526 (2011); doi:10.1016/j.ejmech.2010.11.032.
S. Gemma, G. Kukreja, C. Fattorusso, M. Persico, M.P. Romano, M. Altarelli, L. Savini, G. Campiani, E. Fattorusso, N. Basilico, D. Taramelli, V. Yardley and S. Butini, Bioorg. Med. Chem. Lett., 16, 5384 (2006); doi:10.1016/j.bmcl.2006.07.060.
A. Nayyar, A. Malde, E. Coutinho and R. Jain, Bioorg. Med. Chem., 14, 7302 (2006); doi:10.1016/j.bmc.2006.06.049.
M.K. Mao and J.E. Franz, Synthesis, 920 (1991); doi:10.1055/s-1991-26606.
M. Böger, D. Dürr, L. Gsell, R. G Hall, F. Karrer, O. Kristiansen, P. Maienfisch, A. Pascual and A. Rindlisbacher, Pest Manag. Sci., 57, 191 (2001) doi:10.1002/1526-4998(200102)57:2<191::AID-PS275>3.0.CO;2-O.
J.B. Raoof, R. Ojani and Z. Mohammadpour, Int. J. Electrochem. Soc., 5, 177 (2010).