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Copyright (c) 2014 Gang Li1, Su-Xia Gao2, Zong-Li Ren1, Na Wen1, Li Wang1, Xiu-Yan Dong1
This work is licensed under a Creative Commons Attribution 4.0 International License.
Synthesis and Characterization of Five Bisoxime-Type Chelating Ligands Based on Bis(aminooxy)alkane and 2-Naphthaldehyde
Corresponding Author(s) : Gang Li1
Asian Journal of Chemistry,
Vol. 26 No. 20 (2014)
Abstract
Five bisoxime chelating ligands L1-L5 have been synthesized from 2-naphthaldehyde and 1,2-bis(aminooxy)ethane, 1,3-bis(aminooxy)-propane, 1,4-bis(aminooxy)butane, 1,5-bis(aminooxy)pentane and 1,6-bis(aminooxy)hexane in hot ethanolic medium, respectively and characterized by elemental analyses, IR, UV-visible spectra and 1H NMR spectroscopy. The bisoxime chelating ligands L1-L5 may be promising units for the construction of supramolecular metal complexes.
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- B.H. Mehta and B. Nagarkoti, Asian J. Chem., 14, 103 (2002).
- E.S. Rachaman, Y. Ashani and H. Leader, Arzneimittelforschung, 29, 875 (1979).
- S. Yamada, Coord. Chem. Rev., 190-192, 537 (1999).
- A.K. Sharma, F. Lloret and R. Mukherjee, Inorg. Chem., 46, 5128 (2007).
- Z.L. Ren, W.K. Dong, W.J. Bai, X.N. He and L. Wang, Acta Crystallogr., E64, o1678 (2008).
- X.Y. Dong, Y.X. Sun, L. Wang and L. Li, J. Chem. Res., 36, 387 (2012).
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- H.E. Smith, Chem. Rev., 83, 359 (1983).
References
V.V. Pavlishchuk, S.V. Kolotilov, A.W. Addison, M.J. Prushan, D. Schollmeyer, L.K. Thompson, T. Weyhermüller and E.A. Goreshnik, Dalton Trans., 1587 (2003).
D.T. Rosa, J.A. Krause Bauer and M.J. Baldwin, Inorg. Chem., 40, 1606 (2001).
J. Custot, J.L. Boucher, S. Vadon, C. Guedes, S. Dijols, M. Delaforge and D. Mansuy, J. Biol. Inorg. Chem., 1, 73 (1996).
B.H. Mehta and B. Nagarkoti, Asian J. Chem., 14, 103 (2002).
E.S. Rachaman, Y. Ashani and H. Leader, Arzneimittelforschung, 29, 875 (1979).
S. Yamada, Coord. Chem. Rev., 190-192, 537 (1999).
A.K. Sharma, F. Lloret and R. Mukherjee, Inorg. Chem., 46, 5128 (2007).
Z.L. Ren, W.K. Dong, W.J. Bai, X.N. He and L. Wang, Acta Crystallogr., E64, o1678 (2008).
X.Y. Dong, Y.X. Sun, L. Wang and L. Li, J. Chem. Res., 36, 387 (2012).
(a) W.K. Dong, Y.X. Sun, X.Y. Dong, S.J. Xing and L. Wang, J. Coord. Chem., 66, 3291 (2013); (b) W.K. Dong, L.S. Zhang, Y.X. Sun, M.M. Zhao, G. Li and X.Y. Dong, Spectrochim. Acta A, 121, 324 (2014); (c) W.-K. Dong, J. Yao and Y.X. Sun, Synth. React. Inorg. Met.-Org. Nano-Met. Chem, 41, 177 (2011); (d) W.K. Dong, Y.X. Sun, C.Y. Zhao, X.Y. Dong and L. Xu, Polyhedron, 29, 2087 (2010).
H.E. Smith, Chem. Rev., 83, 359 (1983).