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Synthesis, characterization, crystal structures, and antimicrobial activity of cobalt(II) and iron(III) complexes derived from N'-(2-hydroxybenzylidene)-3-methylbenzohydrazide

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Abstract

A new cobalt(II,III) complex, [CoIIIL2]2[Co II2 (HL)2(OH2)2(CH3OH)2] • 2H2O (I) and a new iron(III) complex, [FeIII(HL)2](NO3) (II), where L2– and HL are the dianionic and monoanionic form of N'-(2-hydroxybenzylidene)-3-methylbenzohydrazide, respectively, have been prepared and characterized by elemental analyses, infrared and UV-Vis spectroscopy and single-cyrstal X-ray diffraction (CIF files CCDC nos. 1417971 (I), 1417979 (II)). Complex I crystallizes in the monoclinic space group P21/n with unit cell dimensions a = 16.1665(9), b = 14.5692(8), c = 19.086(1) Å, β = 96.347(1)°, V = 4467.9(4) Å3, Z = 2, R 1 = 0.0521, and wR 2 = 0.1411. Complex II crystallizes in the orthorhombic space group Pbcn with unit cell dimensions a = 12.475(1), b = 12.202(1), c = 18.859(2) Å, V = 2870.8(4) Å3, Z = 4, R 1 = 0.0796, and wR 2 = 0.1981. The metal atoms in the complexes are in octahedral coordination. Crystals of the complexes are stabilized by hydrogen bonds. The efficiency of the aroylhydrazone and the two complexes was evaluated against B. subtilis, S. aureus, E. coli, P. fluorescence, C. albicans and A. niger, with the complexes demonstrating enhanced activity relatively to the free ligand.

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References

  1. Gavey, E.L. and Pilkington, M., Coord. Chem. Rev., 2015, vol. 296, p. 125.

    Article  CAS  Google Scholar 

  2. Consiglio, G., Oliveri, I.P., Punzo, F., et al., Dalton Trans., 2015, vol. 44, no. 29, p. 13040.

    Article  CAS  Google Scholar 

  3. Lachachi, M.B., Benabdallah, T., Aguiar, P.M., et al., Dalton Trans., 2015, vol. 44, no. 26, p. 11919.

    Article  CAS  Google Scholar 

  4. Aono, Y., Yoshida, H., Katoh, K., et al., Inorg. Chem., 2015, vol. 54, no. 14, p. 7096.

    Article  CAS  Google Scholar 

  5. Khorshidifard, M., Rudbari, H.A., Askari, B., et al., Polyhedron, 2015, vol. 95, p. 1.

    Article  CAS  Google Scholar 

  6. Toledano-Magana, Y., Garcia-Ramos, J.C., Navarro-Olivarria, M., et al., Molecules, 2015, vol. 20, no. 6, p. 9929.

    Article  CAS  Google Scholar 

  7. Kaplanek, R., Havlik, M., Dolensky, B., et al., Bioorg. Med. Chem., 2015, vol. 23, no. 7, p. 1651.

    Article  CAS  Google Scholar 

  8. Rajitha, G., Prasad, K.V.S.R.G., Umamaheswari, A., et al., Med. Chem. Res., 2014, vol. 23, no. 12, p. 5204.

    Article  CAS  Google Scholar 

  9. Altintop, M.D., Ozdemir, A., Ilgin, S., et al., Lett. Drug Des. Discov., 2014, vol. 11, no. 7, p. 833.

    Article  CAS  Google Scholar 

  10. Altintop, M.D., Ozdemir, A., Turan-Zitouni, G., et al., Eur. J. Med. Chem., 2012, vol. 58, p. 299.

    Article  CAS  Google Scholar 

  11. Kaplancikli, Z.A., Altintop, M.D., Ozdemir, A., et al., Lett. Drug. Des. Discov., 2012, vol. 9, no. 3, p. 310.

    Article  CAS  Google Scholar 

  12. Blanot, D., Lee, J., and Girardin, S.E., Chem. Biol. Drug Des., 2012, vol. 79, no. 1, p. 2.

    Article  CAS  Google Scholar 

  13. Chew, S.T., Lo, K.M., Sinniah, S.K., et al., RSC Advances, 2014, vol. 4, no. 106, p. 61232.

    Article  CAS  Google Scholar 

  14. Sheng, G.-H., Han, X., You, Z.L., et al., J. Coord. Chem., 2014, vol. 67, no. 10, p. 1760.

    Article  CAS  Google Scholar 

  15. Tsay, O.G., Manjare, S.T., Kim, H., et al., Inorg. Chem., 2013, vol. 52, no. 17, p. 10052.

    Article  CAS  Google Scholar 

  16. Alagesan, M., Bhuvanesh, N.S.P., and Dharmaraj, N., Dalton Trans., 2013, vol. 42, no. 19, p. 7210.

    Article  CAS  Google Scholar 

  17. Datta, A., Liu, P.-H., Huang, J.-H., et al., Polyhedron, 2012, vol. 44, no. 1, p. 77.

    Article  CAS  Google Scholar 

  18. Al-Shaalan, N.H., Molecules, 2011, vol. 16, no. 10, p. 8629.

    Article  CAS  Google Scholar 

  19. Hegazy, W.H. and Al-Motawaa, I.H., Synth. React. Inorg. Met.-Org. Nano-Met. Chem., 2011, vol. 41, no. 9, p. 1172.

    Article  CAS  Google Scholar 

  20. El-Dissouky, A., Al-Fulaij, O., Awad, M.K., et al., J. Coord. Chem., 2010, vol. 63, no. 2, p. 330.

    Article  CAS  Google Scholar 

  21. Zhang, M., Xian, D.-M., Li, H.-H., et al., Aust. J. Chem., 2012, vol. 65, no. 4, p. 343.

    CAS  Google Scholar 

  22. Ye, Y.-T., Niu, F., Sun, Y., et al., Chin. J. Inorg. Chem., 2015, vol. 31, no. 5, p. 1019.

    CAS  Google Scholar 

  23. Qu, D., Niu, F., Zhao, X.L., et al., Bioorg. Med. Chem., 2015, vol. 23, no. 9, p. 1944.

    Article  CAS  Google Scholar 

  24. Huo, Y., Ye, Y.-T., Cheng, X.-S., et al., Inorg. Chem. Commun., 2014, vol. 45, p. 131.

    Article  CAS  Google Scholar 

  25. Zhao, Y., Han, X., Zhou, X.-X., et al., Chin. J. Inorg. Chem., 2013, vol. 29, no. 4, p. 867.

    CAS  Google Scholar 

  26. Liu, Z.-X., Acta Crystallogr., Sect. E: Struct. Rep. Online, 2011, vol. 67, no. 12, p. o3439.

    Article  CAS  Google Scholar 

  27. SMART and SAINT, Madison: Bruker AXS, Inc., 2002.

  28. Sheldrick, G.M., SADABS, Program for Empirical Absorption Correction of Area Detector, Göttingen: Univ. of Göttingen, 1996.

    Google Scholar 

  29. Sheldrick, G.M., SHELXTL, Version 5.1, Software Reference Manual, Madison: Bruker AXS, Inc., 1997.

    Google Scholar 

  30. Meletiadis, J., Meis, J.F., Mouton, J.W., et al., J. Clin. Microbiol., 2000, vol. 38, no. 8, p. 2949.

    CAS  Google Scholar 

  31. Sebastian, M., Arun, V., Robinson, P.P., et al., J. Coord. Chem., 2010, vol. 63, no. 2, p. 307.

    Article  CAS  Google Scholar 

  32. Shaabani, B., Khandar, A.A., Mobaiyen, H., et al., Polyhedron, 2014, vol. 80, p. 166.

    Article  CAS  Google Scholar 

  33. Sreekanth, A., Kala, U.L., Nayar, C.R., et al., Polyhedron, 2004, vol. 23, no. 1, p. 41.

    Article  CAS  Google Scholar 

  34. Bogdanovic, G.A., Leovac, V.M., Vojinovic-Jesic, L.S., et al., J. Serb. Chem. Soc., 2007, vol. 72, no. 1, p. 63.

    Article  CAS  Google Scholar 

  35. Wu, L.-M., Teng, H.-B., Feng, X.-C., et al., Cryst. Growth Des., 2007, vol. 7, no. 7, p. 1337.

    Article  CAS  Google Scholar 

  36. Sadhukhan, D., Ray, A., Pilet, G., et al., Bull. Chem. Soc. Jpn., 2011, vol. 84, no. 7, p. 764.

    Article  CAS  Google Scholar 

  37. Charkoudian, L.K., Pham, D.M., Kwon, A.M., et al., Dalton Trans., 2007, no. 43, p. 5031.

    Article  Google Scholar 

  38. Matoga, D., Szklarzewicz, J., Stadnicka, K., et al., Inorg. Chem., 2007, vol. 46, no. 22, p. 9042.

    Article  CAS  Google Scholar 

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Correspondence to Z. L. You.

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Yang, T., Niu, F., Li, L.X. et al. Synthesis, characterization, crystal structures, and antimicrobial activity of cobalt(II) and iron(III) complexes derived from N'-(2-hydroxybenzylidene)-3-methylbenzohydrazide. Russ J Coord Chem 42, 402–409 (2016). https://doi.org/10.1134/S1070328416050109

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  • DOI: https://doi.org/10.1134/S1070328416050109

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