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Microwave Solid Phase Synthesis, Characterization and Antimicrobial Activities of Manganese(II) Complex with 2-((Furan-3-ylmethylimino)methyl)phenol
Corresponding Author(s) : Suo-Ping Xu
Asian Journal of Chemistry,
Vol. 27 No. 5 (2015): Vol 27 Issue 5
Abstract
Mononuclear complex of manganese (1) has been designed and synthesized by 2-((furan-3-ylmethylimino)methyl)phenol (L) with MnCl2·4H2O in microwave radiation. The complex was characterized by X-ray crystallography, confirming that the central mangances(II) was coordinated by two oxygen atoms and two nitrogen atoms from two L. 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.
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- 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. Toroglu, E. Ispir and C. Çelik, Asian J. Chem., 19, 5497 (2009).
- 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.
- R.V. Singh, P. Chaudhary, S. Chauhan and M. Swami, Spectrochim. Acta A, 72, 260 (2009); doi:10.1016/j.saa.2008.09.017.
- 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. Toroglu, E. Ispir and C. Çelik, Asian J. Chem., 19, 5497 (2009).
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.
R.V. Singh, P. Chaudhary, S. Chauhan and M. Swami, Spectrochim. Acta A, 72, 260 (2009); doi:10.1016/j.saa.2008.09.017.
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.