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Study of Catalytic Activity of Silica Supported Schiff Base Complexes
Corresponding Author(s) : S.P. Dagade
Asian Journal of Chemistry,
Vol. 29 No. 7 (2017): Vol 29 Issue 7
Abstract
The catalytic activity of silica supported Schiff base metal complexes have been studied for the oxidation of benzyl alcohol, using hydrogen peroxide, which gave benzaldehyde as a major product. Silica supported Schiff base complexes gave better results compared to unsupported Schiff base complexes. Schiff base metal complexes such as Cr(VI), Mo(VI) and W(VI) have played significant role to enhance their conversion and selectivity. Among these Cr(VI) showed better conversion.
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- A.M. Abu-Dief and I.M.A. Mohamed, Beni-Suef Univ. J. Basic Appl. Sci., 4, 119 (2015); https://doi.org/10.1016/j.bjbas.2015.05.004.
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- P. Cozzi, Chem. Soc. Rev., 33, 410 (2004); https://doi.org/10.1039/B307853C.
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- S.P. Dagade, V.B. Mane, A.A. Jape, S.A. Waghmode, V.V. Dhapte and L.H. Mahind, Int. J. Chem. Anal. Sci., 3, 1672 (2012).
References
A.M. Abu-Dief and I.M.A. Mohamed, Beni-Suef Univ. J. Basic Appl. Sci., 4, 119 (2015); https://doi.org/10.1016/j.bjbas.2015.05.004.
P. Pfeiffer, E. Breith, E. Lübbe and T. Tsumaki, Liebigs Ann. Chem., 503, 84 (1993); https://doi.org/10.1002/jlac.19335030106.
T.A. Alsalim, J.S. Hadi, O.N. Ali, H.S. Abbo and S.J.J. Titinchi, Chem. Centr. J., 7, 3 (2013); https://doi.org/10.1186/1752-153X-7-3.
R. Irie, K. Noda, Y. Ito, N. Matsumoto and T. Katsuki, Tetrahedron Lett., 31, 7345 (1990); https://doi.org/10.1016/S0040-4039(00)88562-7.
E.N. Jacobsen, Comprehensive Organometallic Chemistry II, vol. 12, p. 1097 (1995).
N.S. Venkataramanan, G. Kuppuraj and S. Rajagopal, Coord. Chem. Rev., 249, 1249 (2005); https://doi.org/10.1016/j.ccr.2005.01.023.
B.M. Choudary, T. Ramani, H. Maheswaran, L. Prashant, K.V.S. Ranganath and K.V. Kumar, Adv. Synth. Catal., 348, 493 (2006); https://doi.org/10.1002/adsc.200505427.
S. Mohebbi, F. Nikpour and S. Raiati, J. Mol. Catal. Chem., 256, 265 (2006); https://doi.org/10.1016/j.molcata.2006.04.041.
P. Cozzi, Chem. Soc. Rev., 33, 410 (2004); https://doi.org/10.1039/B307853C.
A. Haikarainen, J. Sipila, P. Pietikäinen, A. Pajunen and I. Mutikainen, J. Chem. Soc., Dalton Trans., 991 (2001); https://doi.org/10.1039/b008167l.
W. Zhang, J.L. Loebach, S.R. Wilson and E.N. Jacobsen, J. Am. Chem. Soc., 112, 2801 (1990); https://doi.org/10.1021/ja00163a052.
M. Silva, C. Freire, B. de Castro and J.L. Figueiredo, J. Mol. Catal. Chem., 258, 327 (2006); https://doi.org/10.1016/j.molcata.2006.05.070.
C.T. Dalton, K.M. Ryan, V.M. Wall, C. Bousquet and D.G. Gilheany, Top. Catal., 5, 75 (1998); https://doi.org/10.1023/A:1019102003494.
W. Adam, K.J. Roschmann, C.R. Saha-Möller and D. Seebach, J. Am. Chem. Soc., 124, 5068 (2002); https://doi.org/10.1021/ja0177206.
E.N. Jacobsen and M.H. Wu, in eds.: A. Pfaltz, E.N. Jacobsen and H. Yamamoto, Comprehensive Asymmetric Catalysis, Springer-Verlag, Berlin, vol. 2, p. 649 (1999).
N.H. Khan, S. Agrawal, R.I. Kureshy, S.H.R. Abdi, V.J. Mayani and R.V. Jasra, Tetrahedron Asymm., 17, 2659 (2006); https://doi.org/10.1016/j.tetasy.2006.09.024.
N. Raman, R. Jeyamurugan, M. Subbulakshmi, R. Boominathan and C. Yuvarajan, Chem. Pap., 64, 318 (2010); https://doi.org/10.2478/s11696-010-0003-0.
T. Shamspur, I. Sheikhshoaie and M.H. Mashhadizadeh, J. Anal. At. Spectrom., 20, 476 (2005); https://doi.org/10.1039/B416097E.
S. Priyarega, M.M. Tamizh, R. Karvembu, R. Prabhakaran and K. Natarajan, J. Chem. Sci., 123, 319 (2011); https://doi.org/10.1007/s12039-011-0087-2.
M.R. Ganjali, T. Poursaberi, M. Hosseini, M. Salavati-Niasary, M. Yousefi and M. Shamsipur, Anal. Sci., 18, 289 (2002); https://doi.org/10.2116/analsci.18.289.
M. Tumer, E. Akgun, S. Toroglu, A. Kayraldiz and L. Donbak, J. Coord. Chem., 61, 2935 (2008); https://doi.org/10.1080/00958970801989902.
S.P. Dagade, V.B. Mane, A.A. Jape, S.A. Waghmode, V.V. Dhapte and L.H. Mahind, Int. J. Chem. Anal. Sci., 3, 1672 (2012).