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Microwave Solid Phase Synthesis, Characterization and Antimicrobial Activities of 2,2'-[(1E,1'E)- {ethane-1,2-diylbis(azanylylidene)}bis(methanylylidene)]bis(4-chlorophenol)manganese(II)
Corresponding Author(s) : Suo-Ping Xu
Asian Journal of Chemistry,
Vol. 27 No. 9 (2015): Vol 27 Issue 9
Abstract
One mononuclear complex (1) has been designed and synthesized by 2,2'-[(1E,1'E)-{ethane-1,2- diylbis(azanylylidene)}bis(methanylylidene)]bis(4-chlorophenol) (L) with MnCl2·4H2O in microwave radiation assistance. The complex was characterized by X-ray crystallo-graphy, confirming that the central mangances(II) was coordinated by two oxygen atoms, two nitrogen atoms from L and two oxygen atoms from H2O. The complex was assayed for in vitro antibacterial (B. subtilis, S. aureus, S. faecalis, P. aeruginosa, E. coli and E. cloacae) activities and showed better antimicrobial activity against Gram positive strains than Gram negative strains.
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- S.-P. Xu, L. Shi, P.-C. Lv, R.-Q. Fang and H.-L. Zhu, J. Coord. Chem., 62, 2048 (2009); doi:10.1080/00958970902741251.
- L. Shi, H.-M. Ge, S.-H. Tan, H.-Q. Li, Y.-C. Song, H.-L. Zhu and R.-X. Tan, Eur. J. Med. Chem., 42, 558 (2007); doi:10.1016/j.ejmech.2006.11.010.
- A. Roth, E.T. Spielberg and W. Plass, Inorg. Chem., 46, 4362 (2007); doi:10.1021/ic070088i.
- J.D. Ranford, J.J. Vittal and Y.M. Wang, Inorg. Chem., 37, 1226 (1998); doi:10.1021/ic970805g.
- S.-P. Xu, Y. Pei, G. Xu, W.-X. Su and J.-X. Shu, J. Xuzhou Norm. Univ. Nat. Sci. Ed., 28, 57 (2010).
- L.-M. Wu, H.-B. Teng, X.-C. Feng, X.-B. Ke, Q.-F. Zhu, J.-T. Su, W.-J. Xu and X.-M. Hu, Cryst. Growth Des., 7, 1337 (2007); doi:10.1021/cg070196f.
- S.-P. Xu, P.-C. Lv, L. Shi and H.-L. Zhu, Arch. Pharm. Chem. Life Sci., 343, 282 (2010).
- S.-P. Xu, Y. Pei, G. Xu, W.-X. Su and J.-X. Shu, J. Xuahou Norm. Univ. Nat. Sci. Ed., 28, 57 (2010).
- P. Prusis, M. Dambrova, V. Andrianov, E. Rozhkov, V. Semenikhina, I. Piskunova, E. Ongwae, T. Lundstedt, I. Kalvinsh and J.E.S. Wikberg, J. Med. Chem., 47, 3105 (2004); doi:10.1021/jm031127c.
- S. Ren, R. Wang, K. Komatsu, P. Bonaz-Krause, Y. Zyrianov, C.E. McKenna, C. Csipke, Z.A. Tokes and E.J. Lien, J. Med. Chem., 45, 410 (2002); doi:10.1021/jm010252q.
- P.H. Wang, J.G. Keck, E.J. Lien and M.M.C. Lai, J. Med. Chem., 33, 608 (1990); doi:10.1021/jm00164a023.
- S.-P. Xu, B.-F. Ruan, Q.-Y. Pan and R.-T. Hu, J. Coord. Chem., 64, 2489 (2011); doi:10.1080/00958972.2011.601459.
- G.M. Sheldrick, SHELXL V5.1 Software Reference Manual, Bruker AXS, Inc., Madison, WI, USA (1997).
- J. Meletiadis, J.F. Meis, J.W. Mouton, J.P. Donnelly and P.E. Verweij, J. Clin. Microbiol., 38, 2949 (2000).
- K. Nakamato, Infrared Spectra of Inorganic and Coordination Compounds, Wiley, New York (1994).
- J.-M. Li, J.-Z. Li, H.-Q. Zhang and L.-Y. Xu, Inorg. Chem. Commun., 13, 573 (2010); doi:10.1016/j.inoche.2010.01.023.
- S.-P. Xu, L. Shi, P.-C. Lv, R.-Q. Fang and H.-L. Zhu, J. Coord. Chem., 62, 2048 (2009); doi:10.1080/00958970902741251.
- M. Nath, S. Pokharia, X. Song, G. Eng, M. Gielen, M. Kemmer, M. Biesemans, R. Willem and D. De Vos, Appl. Organomet. Chem., 17, 305 (2003); doi:10.1002/aoc.451.
References
S.-P. Xu, L. Shi, P.-C. Lv, R.-Q. Fang and H.-L. Zhu, J. Coord. Chem., 62, 2048 (2009); doi:10.1080/00958970902741251.
L. Shi, H.-M. Ge, S.-H. Tan, H.-Q. Li, Y.-C. Song, H.-L. Zhu and R.-X. Tan, Eur. J. Med. Chem., 42, 558 (2007); doi:10.1016/j.ejmech.2006.11.010.
A. Roth, E.T. Spielberg and W. Plass, Inorg. Chem., 46, 4362 (2007); doi:10.1021/ic070088i.
J.D. Ranford, J.J. Vittal and Y.M. Wang, Inorg. Chem., 37, 1226 (1998); doi:10.1021/ic970805g.
S.-P. Xu, Y. Pei, G. Xu, W.-X. Su and J.-X. Shu, J. Xuzhou Norm. Univ. Nat. Sci. Ed., 28, 57 (2010).
L.-M. Wu, H.-B. Teng, X.-C. Feng, X.-B. Ke, Q.-F. Zhu, J.-T. Su, W.-J. Xu and X.-M. Hu, Cryst. Growth Des., 7, 1337 (2007); doi:10.1021/cg070196f.
S.-P. Xu, P.-C. Lv, L. Shi and H.-L. Zhu, Arch. Pharm. Chem. Life Sci., 343, 282 (2010).
S.-P. Xu, Y. Pei, G. Xu, W.-X. Su and J.-X. Shu, J. Xuahou Norm. Univ. Nat. Sci. Ed., 28, 57 (2010).
P. Prusis, M. Dambrova, V. Andrianov, E. Rozhkov, V. Semenikhina, I. Piskunova, E. Ongwae, T. Lundstedt, I. Kalvinsh and J.E.S. Wikberg, J. Med. Chem., 47, 3105 (2004); doi:10.1021/jm031127c.
S. Ren, R. Wang, K. Komatsu, P. Bonaz-Krause, Y. Zyrianov, C.E. McKenna, C. Csipke, Z.A. Tokes and E.J. Lien, J. Med. Chem., 45, 410 (2002); doi:10.1021/jm010252q.
P.H. Wang, J.G. Keck, E.J. Lien and M.M.C. Lai, J. Med. Chem., 33, 608 (1990); doi:10.1021/jm00164a023.
S.-P. Xu, B.-F. Ruan, Q.-Y. Pan and R.-T. Hu, J. Coord. Chem., 64, 2489 (2011); doi:10.1080/00958972.2011.601459.
G.M. Sheldrick, SHELXL V5.1 Software Reference Manual, Bruker AXS, Inc., Madison, WI, USA (1997).
J. Meletiadis, J.F. Meis, J.W. Mouton, J.P. Donnelly and P.E. Verweij, J. Clin. Microbiol., 38, 2949 (2000).
K. Nakamato, Infrared Spectra of Inorganic and Coordination Compounds, Wiley, New York (1994).
J.-M. Li, J.-Z. Li, H.-Q. Zhang and L.-Y. Xu, Inorg. Chem. Commun., 13, 573 (2010); doi:10.1016/j.inoche.2010.01.023.
S.-P. Xu, L. Shi, P.-C. Lv, R.-Q. Fang and H.-L. Zhu, J. Coord. Chem., 62, 2048 (2009); doi:10.1080/00958970902741251.
M. Nath, S. Pokharia, X. Song, G. Eng, M. Gielen, M. Kemmer, M. Biesemans, R. Willem and D. De Vos, Appl. Organomet. Chem., 17, 305 (2003); doi:10.1002/aoc.451.