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Copyright (c) 2014 Bo-Xian Jin1, Su-Xia Gao2, Wei-Min Zhou1, Gao-Xian An1, Yang Bai1, Wei Du1, Xiu-Yan Dong1
This work is licensed under a Creative Commons Attribution 4.0 International License.
Bromo-Substituted Salamo-Type Compounds Possessing More Flexible O-Alkyl Chain: Synthesis and Sructural Characterization
Corresponding Author(s) : Bo-Xian Jin1
Asian Journal of Chemistry,
Vol. 26 No. 20 (2014)
Abstract
A series of bromo-substituted Salamo-type compounds have been synthesized by the reaction of 5-bromo-2-hydroxybenzaldehyde with 1,7-bis(aminooxy)heptane, 1,8-bis(aminooxy)octane, 1,9-bis(aminooxy)nonane or 1,10-bis(aminooxy)decane in hot ethanol medium, respectively, and characterized by elemental analyses, IR, UV-visible spectra and 1H NMR spectroscopy.
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- C. Meermann, K.W. Törnroos and R. Anwander, Inorg. Chem., 48, 2561 (2009).
- J. Tisato, F. Refosco and F. Bandoli, Coord. Chem. Rev., 135-136, 325 (1994).
- S.S. Sundari, A. Dhathathreyan, M. Kanthimathi and B.U. Nair, Langmuir, 13, 4923 (1997).
- W.K. Dong, G. Wang, S.S. Gong, J.F. Tong, Y.X. Sun and X.H. Gao, Transition Met. Chem., 37, 271 (2012).
- W.K. Dong, Y.X. Sun, Y.P. Zhang, L. Li, X.N. He and X.L. Tang, Inorg. Chim. Acta, 362, 117 (2009).
- N.S. Venkataramanan, G. Kuppuraj and S. Rajagopal, Coord. Chem. Rev., 249, 1249 (2005).
- P.G. Lacroix, Eur. J. Inorg. Chem., 2001, 339 (2001).
- S.S. Sun, C.L. Stern, S.T. Nguyen and J.T. Hupp, J. Am. Chem. Soc., 126, 6314 (2004).
- 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).
- W.K. Dong and J.G. Duan, J. Coord. Chem., 61, 781 (2008).
- W.K. Dong, J.H. Feng and X.Q. Yang, Synth. React. Inorg. Met.-Org. Nano-Met. Chem, 37, 189 (2007).
- W.K. Dong, Y.X. Sun, C.Y. Zhao, X.Y. Dong and L. Xu, Polyhedron, 29, 2087 (2010).
- T. Ghosh, B. Mondal, T. Ghosh, M. Sutradhar, G. Mukherjee and M. Drew, Inorg. Chim. Acta, 360, 1753 (2007).
- W.K. Dong, S.J. Xing, Y.X. Sun, L. Zhao, L.Q. Chai and X.H. Gao, J. Coord. Chem., 65, 1212 (2012).
- J.A. Faniran, K.S. Patel and J.C. Bailar Jr., J. Inorg. Nucl. Chem., 36, 1547 (1974).
- H.E. Smith, Chem. Rev., 83, 359 (1983).
- S. Akine, T. Taniguchi and T. Nabeshima, Chem. Lett., 30, 682 (2001).
References
C. Meermann, K.W. Törnroos and R. Anwander, Inorg. Chem., 48, 2561 (2009).
J. Tisato, F. Refosco and F. Bandoli, Coord. Chem. Rev., 135-136, 325 (1994).
S.S. Sundari, A. Dhathathreyan, M. Kanthimathi and B.U. Nair, Langmuir, 13, 4923 (1997).
W.K. Dong, G. Wang, S.S. Gong, J.F. Tong, Y.X. Sun and X.H. Gao, Transition Met. Chem., 37, 271 (2012).
W.K. Dong, Y.X. Sun, Y.P. Zhang, L. Li, X.N. He and X.L. Tang, Inorg. Chim. Acta, 362, 117 (2009).
N.S. Venkataramanan, G. Kuppuraj and S. Rajagopal, Coord. Chem. Rev., 249, 1249 (2005).
P.G. Lacroix, Eur. J. Inorg. Chem., 2001, 339 (2001).
S.S. Sun, C.L. Stern, S.T. Nguyen and J.T. Hupp, J. Am. Chem. Soc., 126, 6314 (2004).
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).
W.K. Dong and J.G. Duan, J. Coord. Chem., 61, 781 (2008).
W.K. Dong, J.H. Feng and X.Q. Yang, Synth. React. Inorg. Met.-Org. Nano-Met. Chem, 37, 189 (2007).
W.K. Dong, Y.X. Sun, C.Y. Zhao, X.Y. Dong and L. Xu, Polyhedron, 29, 2087 (2010).
T. Ghosh, B. Mondal, T. Ghosh, M. Sutradhar, G. Mukherjee and M. Drew, Inorg. Chim. Acta, 360, 1753 (2007).
W.K. Dong, S.J. Xing, Y.X. Sun, L. Zhao, L.Q. Chai and X.H. Gao, J. Coord. Chem., 65, 1212 (2012).
J.A. Faniran, K.S. Patel and J.C. Bailar Jr., J. Inorg. Nucl. Chem., 36, 1547 (1974).
H.E. Smith, Chem. Rev., 83, 359 (1983).
S. Akine, T. Taniguchi and T. Nabeshima, Chem. Lett., 30, 682 (2001).