European Journal of Chemistry

Synthesis, structural characterization and biological properties of Cu(II), Ni(II), Mn(II), Zn(II) and VO(II) complexes of tetradentate Schiff bases



Main Article Content

Subramanian Vedanayaki
Poomalai Jayaseelan

Abstract

New binucleating Cu(II), Ni(II), Mn(II), Zn(II) and VO(II) complexes of the prepared ligands with N4 donor were synthesized. The ligands are obtained by the condensation of para-phenylenediamine with diacetylmonoxime and benzilmonoxime. The synthesized ligands and their metal complexes were characterized by elemental analysis and various spectroscopic techniques. The Cu(II), Ni(II) complexes were square planar, VO(II) complex was square pyramidal, whereas Mn(II), Zn(II) complexes were of tedrahedral geometry. Both the ligands and their metal complexes were screened for their antibacterial and antifungal activities by minimum inhibitory concentration method. The results showed that the metal complexes were found to be more active than free ligand. The DNA binding capacities of all the complexes were analyzed by using UV absorption spectra. The DNA cleaving capacities of all complexes were analyzed by agarose gel electrophoresis method against pBR322 DNA.


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Vedanayaki, S.; Jayaseelan, P. Synthesis, Structural Characterization and Biological Properties of Cu(II), Ni(II), Mn(II), Zn(II) and VO(II) Complexes of Tetradentate Schiff Bases. Eur. J. Chem. 2016, 7, 368-374.

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References

[1]. Priyarega, S.; Senthil, R. D.; Ganesh, B. S.; Karvembu, R.; Hashimoto, T.; Endo, A.; Natarajan, K. Polyhedron 2012, 34, 143-148.
http://dx.doi.org/10.1016/j.poly.2011.12.017

[2]. Prabu, R.; Vijayaraj, A.; Suresh, R.; Shenbhagaraman, R.; Kaviyarasan, V.; Narayanan, V. Spectrochim. Acta A 2011, 78, 601-606.
http://dx.doi.org/10.1016/j.saa.2010.11.029

[3]. Naderi, E.; Jafari, A. H.; Ehteshamzadeh, M.; Hosseini, M. G. Mater. Chem. Phys. 2009, 115, 852-858.
http://dx.doi.org/10.1016/j.matchemphys.2009.03.002

[4]. Mistry, B. M.; Jauhari, S. Res. Chem. Intermed. 2013, 39, 1049-1068.
http://dx.doi.org/10.1007/s11164-012-0666-y

[5]. Chena, X.; Yamaguchi, A.; Namekawa, M.; Kamijoa, T.; Teramae, N.; Tong, A. Anal. Chim. Acta 2011, 696, 94-100.
http://dx.doi.org/10.1016/j.aca.2011.04.002

[6]. Joseph, J.; Nagashri, K.; BoomadeviJanaki, G. Eur. J. Med. Chem. 2012, 49, 151-163.
http://dx.doi.org/10.1016/j.ejmech.2012.01.006

[7]. Muniyandi, V.; Pravin, N.; Mitu, L.; Raman, N. J. Mol. Struc. 2015, 1086, 56-63.
http://dx.doi.org/10.1016/j.molstruc.2015.01.011

[8]. Kamath, A.; Naik, K.; Netalkar, S. P.; Kokare, D. G.; Revanka, V. K. Med. Chem. Res. 2013, 22, 1948-1956.
http://dx.doi.org/10.1007/s00044-012-0199-3

[9]. Farag, A. M.; Guan, T. S.; Osman, H.; Abdul, M. S.; Iqbal, M. A.; Khadeer, A. M. B. Med. Chem. Res. 2013, 22, 4727-4736.
http://dx.doi.org/10.1007/s00044-013-0482-y

[10]. Jayaseelan, P.; Prasad, S.; Vedanayaki, S.; Rajavel, R. Arabian J. Chem. 2011, DOI: 10.1016/j.arabjc.2011.07.029.
http://dx.doi.org/10.1016/j.arabjc.2011.07.029

[11]. Akila, E.; Usharani, M.; Ramachandran, S.; Jayaseelan, P.; Velraj, G.; Rajavel, R. Arabian J. Chem. 2013, DOI: 10.1016/j.arabjc.2013.11.031.
http://dx.doi.org/10.1016/j.arabjc.2013.11.031

[12]. Chen, Z.; Zhang, J.; Zhang, S. New J. Chem. 2015, 39, 1814-1821.
http://dx.doi.org/10.1039/C4NJ01623H

[13]. Krishna, M. P.; Hussain, R. K.; Prakash, P. J.; Siddavattam, D. Trans. Metal Chem. 2008, 33, 661-668.
http://dx.doi.org/10.1007/s11243-008-9094-7

[14]. Mohini, Y.; Prasad, R. B. N.; Karuna, M. S. L.; Ganesh, K. C.; Poornima, M.; Sujitha P. Med. Chem. Res. 2013, 22, 4360-4366.
http://dx.doi.org/10.1007/s00044-012-0450-y

[15]. Sumrra, S. H.; Chohan, Z. H. Med. Chem. Res. 2013, 22, 3934-3942.
http://dx.doi.org/10.1007/s00044-012-0388-0

[16]. Lahiri, D.; Majumdar, R.; Patra, K.; Chakravarty, A. R. J. Chem. Sci. 2010, 122(3), 321-333.
http://dx.doi.org/10.1007/s12039-010-0037-4

[17]. Joseph, J.; Nagashri, K.; Bibin, R. G. A. J. Saudi Chem. Soc. 2013, 17(3), 285-294.
http://dx.doi.org/10.1016/j.jscs.2011.04.007

[18]. Marmur J. J. Mole. Biol. 1961, 3, 208-214.

[19]. Anbu, S.; Kamalraj, S.; Varghese, B.; Muthumary, J.; Kandaswamy, M. Inorg. Chem. 2012, 51, 5580-5592.
http://dx.doi.org/10.1021/ic202451e

[20]. Shivakumar, L.; Shivaprasad, K.; Revanasiddappa, H. D. Spectrochim. Acta A 2012, 97, 659-666.
http://dx.doi.org/10.1016/j.saa.2012.07.015

[21]. Souaya, E. R.; Hanna, W. G.; Ismail, E. H.; Milad, N. E. Molecules 2000, 5(10), 1121-1129.
http://dx.doi.org/10.3390/51001121

[22]. Lever, A. B. P. Inorganic electronic spectroscopy, Elsevier, Amsterdam, New York, 1984.

[23]. Sathyanarayana, E. N. Electronic absorption spectroscopy and related techniques, UniversityPress (India) limited, Hyderabad, 2001.

[24]. Kivelson, D.; Neiman, R. J. Chem. Phys. 1961, 35, 149-155.
http://dx.doi.org/10.1063/1.1731880

[25]. Abdel-Aiz, A. A.; Salem, A.N.M.; Sayed, M.A.; Abolay, M.N. Mol. Struct. 2012, 1010, 130-138.
http://dx.doi.org/10.1016/j.molstruc.2011.11.043

[26]. Hathaway, B. J.; Bardley, J. N.; Gillard, R. D. Essays in Chemistry, Academic Press Eds. New York, USA, 1971.

[27]. Tweedy, B. G. Phytopathalogy 1964, 55, 910-914.

[28]. Silva, C. M.; Silva, D. L.; Modolo, L. V.; Alves, R. B.; Resende, M. A.; Martins, C. V. B. Fatima, A. J. Adv. Res. 2011, 2, 1-8.

[29]. Arjmand, F.; Sayeed, F.; Muddassir, M. J. Photochem. Photobiol. B: Biol. 2011, 103, 166-179.
http://dx.doi.org/10.1016/j.jphotobiol.2011.03.001

[30]. Iqbal, M.; Ali, S.; Rehman, Z.; Muhammad, N.; Sohail, M.; Pandarinathan, V. J. Mol. Struc. 2015, 1093, 135-143.
http://dx.doi.org/10.1016/j.molstruc.2015.03.058

[31]. Sobha, S.; Mahalakshmi, R.; Raman, N. Spectrochim. Acta A 2012, 92, 175-183.
http://dx.doi.org/10.1016/j.saa.2012.02.063

[32]. Vilson, K.; Walker, J. Principles and Techniques of Biochemistry and Molecular biology, Seventh edn., Cambridge University Press, India, 2010.

[33]. Lin, Y.; Cho, H.; Tan, L.; Yuan, Y.; Wei, W.; Ji, L. J. Inorg. Biochem. 2005, 99, 530-537.
http://dx.doi.org/10.1016/j.jinorgbio.2004.10.030

[34]. Jayaseelan. P.; Akila, E.; Usha, R. M.; Rajavel, R. J. Saudi Chem. Soc. 2013. DOI:10.1016/j.jscs.2013.07.001.
http://dx.doi.org/10.1016/j.jscs.2013.07.001

Supporting Agencies

University Grant Commission (MRP-5388/14 (SERO/UGC), March 2014, Com.code TNPE004), Hyderabad, India.
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