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Synthesis and Characterization of Salamo-Type Bisoxime Compounds Bearing Nitro Group
Corresponding Author(s) : Gang Li
Asian Journal of Chemistry,
Vol. 25 No. 15 (2013): Vol 25 Issue 15
Abstract
A series of nitro salamo-type bisoxime compounds have been synthesized from 2-hydroxy-5-nitrobenzaldehyde and 1,6-bis(amino-oxy)hexane, 1,7-bis(aminooxy)heptane, 1,8-bis(aminooxy)octane or 1,10-bis(aminooxy)decane in ethanolic medium, respectively and characterized by elemental analyses as well as by IR, UV-visible and 1H NMR spectroscopy. Salamo-type bisoxime compound is much more useful to assemble supramolecular systems than a Salen moiety.
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- A.M. Castilla, S. Curreli, E.C. Escudero-Adán, M.M. Belmonte, J. BenetBuchholz and A.W. Kleij, Org. Lett., 11, 5218 (2009).
- Z. Li and C. Jablonski, Inorg. Chem., 39, 2456 (2000).
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- L.C.F. Humphrey, C. Rodolphe, K.P. Annie and B. Sally, Inorg. Chem., 50, 4232 (2011).
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- T. Mizuno, M. Takeuchi and S. Shinkai, Tetrahedron, 55, 9455 (1999).
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- S. Akine, T. Tadokoro and T. Nabeshima,Inorg. Chem., 51, 11478 (2012).
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References
A.M. Castilla, S. Curreli, E.C. Escudero-Adán, M.M. Belmonte, J. BenetBuchholz and A.W. Kleij, Org. Lett., 11, 5218 (2009).
Z. Li and C. Jablonski, Inorg. Chem., 39, 2456 (2000).
J. Gao, J.H. Reibenspies, R.A. Zingaro, F.R. Woolley, A.E. Martell and A. Clearfield, Inorg. Chem., 44, 232 (2005).
T. Glaser, M. Heidemeier, E. Krickemeyer, H. Bögge, A. Stammler, R. Fröhlich, E. Bill and J. Schnack, Inorg. Chem., 48, 607 (2009).
L.C.F. Humphrey, C. Rodolphe, K.P. Annie and B. Sally, Inorg. Chem., 50, 4232 (2011).
(a) E.N. Jacobsen, W. Zhang, A.R. Muci, J.R. Ecker and L. Deng, J. Am. Chem. Soc., 113, 7063 (1991); (b) T. Katsuki, Coord. Chem. Rev., 140, 189 (1995); (c) P. Zhang, M. Yang and X.P. Lu, Asian J. Chem., 19, 2083 (2007).
T. Mizuno, M. Takeuchi and S. Shinkai, Tetrahedron, 55, 9455 (1999).
S. Akine, T. Taniguchi and T. Nabeshima, Chem. Lett., 30, 682 (2001).
S. Akine, T. Tadokoro and T. Nabeshima,Inorg. Chem., 51, 11478 (2012).
S. Akine, S. Hotate and T. Nabeshima, J. Am. Chem. Soc., 133, 13868 (2011).
(a) W.K. Dong, Y.X. Sun, C.Y. Zhao, X.Y. Dong and L. Xu, Polyhedron, 29, 2087 (2010); (b) W.K. Dong, Y.X. Sun, Y.P. Zhang, L. Li, X.N. He and X.L. Tang, Inorg. Chim. Acta, 362, 117 (2009); (c) W.K. Dong, X.N. He, H.B. Yan, Z.W. Lv, X. Chen, C.Y. Zhao and X.L. Tang, Polyhedron, 28, 1419 (2009); (d) W.K. Dong, Y.X. Sun, Y.P. Zhang, L. Li, X.N. He and X.L. Tang, Inorg. Chim. Acta, 362, 117 (2009); (e) W.K. Dong, C.Y. Zhao, Y.X. Sun, X.L. Tang and X.N. He, Inorg. Chem. Commun., 12, 234 (2009); (f) W.K. Dong, Y.X. Sun, X.N. He, J.F. Tong and J.C. Wu, Spectrochim. Acta A, 76, 476 (2010); (g) W.K. Dong, S.J. Xing, Y.X. Sun, L. Zhao, L.Q. Chai and X.H. Gao, J. Coord. Chem., 65, 1212 (2012); (h) W.K. Dong, Y.X. Sun, S.J. Xing, Y. Wang and X.H. Gao, Z. Naturforsch., 67b, 197 (2012); (i) W.K. Dong, Y.X. Sun, G.H. Liu, L. Li, X.Y. Dong and X.H. Gao, Z. Anorg. Allg. Chem., 638, 1370 (2012).
S. Akine, T. Taniguchi, W.K. Dong and T. Nabeshima, J. Org. Chem., 70, 1704 (2005).
J.A. Faniran, K.S. Patel and J.C. Bailar Jr., J. Inorg. Nucl. Chem., 36, 1547 (1974).
T. Ghosh, B. Mondal, T. Ghosh, M. Sutradhar, G. Mukherjee and M. Drew, Inorg. Chim. Acta, 360, 1753 (2007).
H.E. Smith, Chem. Rev., 83, 359 (1983)