نوع مقاله : مقاله علمی پژوهشی
نویسندگان
1 گروه شیمی معدنی، دانشکده شیمی، دانشگاه مازندران، بابلسر، ایران
2 گروه زیست شناسی سلولی و مولکولی، دانشکده علوم پایه، دانشگاه مازندران، بابلسر، ایران
چکیده
کلیدواژهها
عنوان مقاله [English]
نویسندگان [English]
In the study, reaction of the 4-methoxy salicylaldehyde 2-aminobenzoylhydrazone(H2L) with MoO2(acac)2 formed a 5-coordinate Molybdenum(VI) complex [MoO2L]. The synthesized complex and its ligand were characterized with various techniques such as NMR, UV-Vis, FT-IR Spectroscopy and elemental analysis (CHN). Molecular structure of Mo(VI) complex is determined by X-ray crystallography , indicating the dianionic tridentate. The crystallographic data revealed a distorted square-pyramidal geometry.The biological activities of Schiff base ligand, H2L, and the biological role of Mo(VI) metal ion in vitro conditions against four strains of bacterial standard Gram positive and Gram negative investigated. The results indicated that the highest antibacterial activity against Escherichia coli was related to the MoO2L complex. The results of the present study showed that the complex had a stronger antibacterial activity than ligand.
کلیدواژهها [English]
[1] G. G. Mohamed, M. Zayed , S. Abdallah, J. Mol. Struct. 979 (2010) 62.
[2] Z. Kazemi, H. A. Rudbari, M. Sahihi, V. Mirkhani, M. Moghadam, S. Tangestaninejad, I.
Mohammadpoor-Baltork , A.A. Kajani, Polyhedron 170 (2019) 70.
[3] W. Al Zoubi, Int. J. Org. Chem. 3 (2013) 73.
[4] C. Chah, T. Ravoof , A. Veerakumarasivam, Pertanika J. Sci. Technol. 26 (2018) 653.
[5] J. Pisk, L. Bilić, M. Đaković, D. Cvijanović, V. Damjanović, J. Lovrić, M. Rubčić, V. Vrdoljak , M.
Cindrić, Polyhedron 145 (2018) 70.
[6] S.Y. Ebrahimipour, M. Khosravan, J. White , S. Fekri, Appl. Organomet. Chem. 32 (2018) e4233.
[7] E. M. Zayed , M. Zayed, Spectrochim. Acta. A 143 (2015) 81.
[8] H. kargar, A. Adabi Ardakani, N. Feizi, J. Appl. Chem 14 (1398) 9, in Persian. (This style is for
Persian Journal Papers)
[9] L.V. Tamayo, A.F. Santos, I.P. Ferreira, V.G. Santos, M.T. Lopes , H. Beraldo, BioMetals 30 (2017)
379.
[10] A. M. Buysse, M. C. Yap, R. Hunter, J. Babcock , X. Huang, Pest. Manag. Sci. 73 (2017) 782.
[11] R. Fekri, M. Salehi, A. Asadi , M. Kubicki, Inorganica. Chemi. Acta. 484 (2019) 245.
[12] A. Wood, W. Aris , D.J. Brook, Inorg. Chemi. 43 (2004) 8355.
[13] S. Ta, M. Ghosh, K. Ghosh, P. Brandão, V. Félix, S.K. Hira, P.P. Manna , D. Das, ACS Appl. Bio
Mater. 2 (2019) 2802.
[14] J. Sharma, P. Dogra, N. Sharma , Ajay, in AIP Conference Proceedings. 2019. AIP Publishing.
[15] S. Gatti, A. Agostini, U.C. Palmiero, C. Colombo, M. Peviani, A. Biffi , D. Moscatelli,
Nanotechnology 29 (2018) 305602.
[16] N. El Guesmi, S.A. Ahmed, F. Maurel, I.I. Althagafi , K.S. Khairou, J. Photochem. Photobiol. 356
(2018) 272.
[17] K. Mohammadiannejad, R. Ranjbar-Karimi , F. Haghighat, Polycyclic Aromat. Compd. 1
(2019) 1.
[18] M. M. Shakdofa, M. H. Shtaiwi, N. Morsy , T. Abdel-rassel, Main Group. Chem. 13 (2014) 187.
[19] P. Kaufmann, B. R. Duffus, B. Mitrova, C. Iobbi-Nivol, C. Teutloff, M. Nimtz, L. Jänsch, U.
Wollenberger , S. Leimkühler, Biochemistry 57 (2018) 1130.
[20] M. Shukor, M. Halmi, M. Rahman, N. Shamaan , M. Syed, Bio Med. Res. Int. 2014 (2014) 1.
[21] J. Zhang, P. Jiang, Y. Shen, W. Zhang , X. Li, Microporous Mesoporous Mat. 206 (2015) 161.
[22] N. Monadi, E. Ghasmei Gorji, M. Mohseni, J. Appl. Chem 11 (1395) 119.
[23] K. Andjelković, M. Šumar , I. Ivanović-Burmazović, J. Therm. Anal. Calorim. 66 (2001) 759.
[24] S. Pasayat, S.P. Dash, S. Roy, R. Dinda, S. Dhaka, M.R. Maurya, W. Kaminsky, Y.P. Patil , M.
Nethaji, Polyhedron 67 (2014) 1.
[25] R. Kia , H. Kargar, J. Coord. Chem. 68 (2015) 1441.
[26] X-AREA, version 1.30, program for the acquisition and analysis of data, Stoe & Cie GmbH,
Darmstadt, Germany, 2005.
[27] X-RED, version 1.28b, program for data reduction and absorption correction, Stoe & Cie GmbH,
Darmstadt, Germany, 2005.
[28] X-SHAPE, Version 2.05, program for crystal optimization for numerical absorption correction,
Stoe & Cie GmbH, Darmstadt, Germany, 2004.
[29] M. C. Burla, R. Caliandro, M. Camalli, B. Carrozzini, G.L. Cascarano, L. De Caro, C. Giacovazzo,
[30] G. M. Sheldrick, Acta. cryst. A. Found. Cryst. 64 (2008) 112.
[31] G. J. Chen, J.W. McDonald , W. Newton, Inorg. Chemi. 15 (1976) 2612.
[32] M. Ghaemy, B. Aghakhani, M. Taghavi, S.M.A. Nasab , M. Mohseni, React. Funct. Polym, 73
(2013) 555.
[33] M. Sutradhar, T. R. Barman, S. Ghosh , M.G. Drew, J. Mol. Struct. 1020 (2012) 148.
[34] P. Vicini, F. Zani, P. Cozzini , I. Doytchinova, Eur. J. Med. Chem. 37 (2002) 553.
[35] A. Rana, R. Dinda, S. Ghosh , A.J. Blake, Polyhedron 22 (2003) 3075.
[36] T.A. Hanna, A.K. Ghosh, C. Ibarra, M.A. Mendez-Rojas, A.L. Rheingold , W.H. Watson, Inorg.
Chemi. 43 (2004) 1511.
[37] A. Mohammadi, A.H. Doctorsafaei, S.B. Burujeny, H.A. Rudbari, N. Kordestani , S. A. A.
Najafabadi, Chem. Eng. J. 381 (2020) 122776.
[38] P. K. Panchal, P. B. Pansuriya , M. Patel, J. Enzyme. Inhib. Med. Chem 21 (2006) 453.
[39] C. M. Da Silva, D. L. da Silva, L.V. Modolo, R. B. Alves, M. A. de Resende, C.V. Martins , Â. de
Fátima, J. Adv. Res 2 (2011) 1.
[40] H. Ünver, M. Yıldız, B. Dülger, Ö. Özgen, E. Kendi , T.N. Durlu, J. Mol. Struct. 737 (2005) 159.
[41] S. Arulmurugan, H.P. Kavitha , B. Venkatraman, Rasayan. J. Chem. 3 (2010) 385.
[42] K. Dhahagani, S.M. Kumar, G. Chakkaravarthi, K. Anitha, J. Rajesh, A. Ramu , G. Rajagopal, Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 117 (2014) 87.
)