Biologically vital metal-based antimicrobial active mixed ligand complexes: synthesis, characterization, DNA binding and cleavage studies
محورهای موضوعی : Journal of the Iranian Chemical ResearchNatarajan Raman 1 , Ramaraj Jeyamurugan 2 , Arumhgam Sakthivel 3 , Rajendran Antony 4
1 - Research Department of Chemistry, VHNSN College, Virudhunagar-626 001, India
2 - Research Department of Chemistry, VHNSN College, Virudhunagar-626 001, India
3 - Research Department of Chemistry, VHNSN College, Virudhunagar-626 001, India
4 - Research Department of Chemistry, VHNSN College, Virudhunagar-626 001, India
کلید واژه: β-diketone, Complexes, DNA binding, Oxidative cleavage, Antimicrobial,
چکیده مقاله :
Few novel cobalt(II) and copper(II) complexes [M(fmp)3]Cl2, [M(fmp)(bpy)2]Cl2,[M(fmp)(phen)2]Cl2 and [M(fmp)(phen)(bpy)]Cl2 (fmp = 3-furan-2-ylmethylene-pentane-2,4-dione, phen = 1,10-phenanthroline, bpy = 2,2'-bipyridine) have been synthesized andcharacterized by elemental analyses, molar conductance, magnetic susceptibility measurements,IR, electronic, EPR, mass spectra and cyclic voltammetric studies. The synthesized complexesare found to be monomeric and electrolytic nature. The UV-Vis., magnetic susceptibility andEPR spectral data of the complexes suggest a distorted octahedral geometry for Cu(II)complexes and octahedral geometry for Co(II) complexes around the central metal ion. The CVprofile of the complexes shows a quasi-reversible peak which indicates that the metal-ligandlinkage is more covalent in nature. Spectroscopic and viscosity measurements prove that the[M(fmp)(phen)2]Cl2 complexes bind more efficiently with DNA than other complexes throughintercalative mode. The difference of peak potential and electrochemical parameters betweenfree and DNA-bound complexes shows the formation of an electrochemical active complexbetween synthesized complexes and DNA. All the complexes cleave the Supercoiled pUC19DNA in vitro under the presence of reducing agent (3-mercaptopropionic acid). The in vitroantimicrobial activities of the compounds have been tested against the bacterial and fungalstrains using the disc diffusion method. The minimum inhibitory concentration (MIC) valuesagainst the growth of microorganisms are much larger for metal chelates than the individualligands.
[1] R.N. Prasad, M. Agarwal, S. Sharma, Indian J. Chem. 43A (2004) 337-340.
[2] N.K. Singh, S.K. Kushawaha, Indian J. Chem. 43A (2004) 333-336.
[3] N. Raman, V. Muthuraj, S. Ravichandran, A. Kulandaisamy, Proc. Indian Acad. Sci. 115 (2003) 161-
167.
[4] A.V. Ablov, Russ. J. Inorg. Chem. 6 (1961) 157-161.
[5] S. Brini, R. Bucci, V. Carunchio, G. Grassinistrazza, J. Coord. Chem. 17 (1988) 221-226.
[6] E. Casassas, A. Izquierdo-Ridora, R. Tauler, J. Chem. Soc., Dalton Trans. (1990) 2341-2345.
[7] W.R. Mc Whinnie, J. Chem. Soc. (1964) 5165-5169.
[8] R.R. Osborne, W.R. Mc Whinnie, J. Chem. Soc. (1967) 2075-2078.
[9] D.P. Segers, M.K. De Armond, J. Phy. Chem. 86 (1982) 3768-3776.
[10] A. Sengul, Turk. J. Chem. 28 (2004) 703-713.
[11] D.D. Perrin, W.L.F. Armarego, D.R. Perrin, Purification of Laboratory Chemicals, Pergamon Press,
Oxford, 1980.
[12] J. Marmur J. Mol. Biol. 3 (1961) 208-218.
[13] M.E. Reichmann, S.A. Rice, C.A. Thomas, P. Doty, J. Am. Chem. Soc. 76 (1954) 3047-3053.
[14] B. Charies, N. Dattagupta, D.M. Crothers, Biochemistry, 21 (1982) 3933-3937.
[15] S. Satyanarayana, J.C. Daborusak, J.B. Charies, Biochemistry, 32 (1983) 2573-2584.
[16] M.J. Pelzar, E.C.S. Chan, N.R. Krieg, Antibiotics and Other Chemotherapeutic Agents, in
Mirobiology, 5th Edn., Blackwell Science: New York, 1998.
[17] M. Yamashita,Y. Watanabe,T-a. Mitsudo, Y. Takegami, Bull. Chem. Soc, Jpn. 51 (1978) 835-838.
[18] N. Ren, J-J. Zhang, S-L. Xu, R-F. Wang, S-P. Wang, Thermochim. Acta, 438 (2005) 172-177.
[19] J.J. Zhang, N. Ren, Y.X. Wang, S.L. Xu, R.F. Wang, S.P. Wang, J. Braz. Chem. Soc. 17 (2006)
1355-1359.
[20] M. Thomas, M.K.M. Nair, K. Radhakrishnan, Synth. React. Inorg. Met.-Org. Chem. 25 (1995) 471-
479.
[21] C. Spinu, M. Pleniceanu, C. Tigae, Turk. J. Chem. 32 (2008) 487-493.
[22] S. Akine, T. Taniguchi, T. Nabeshima, Inorg. Chem. 43 (2004) 6142-6144.
[23] C.R. Saha, S.K. Hoga, Indian J. Chem. (1986) 340-345.
[24] Y. Prasanthi, K. Kiranmai, N.J.P. Subhashini, Shivaraj, Spectrochim. Acta, 70A (2008) 30-35.
[25] F. Firdaus, K. Fatma, M. Azam, S.N. Khan, A.U. Khan, M. Shakir, Transition Met. Chem. 33
(2008) 467-473.
[26] R.M. Kadam, M.D. Sastry, M.K. Bhide, S.A. Chavan, J.V. Yakhmi, O. Khan, Chem. Phys. Lett.
281 (1997) 292-296.
[27] K. Jeyasubramanian, S.A. Samath, S. Thambidurai, R. Murugesan, S.K. Ramalingam, Transition
Met. Chem. 20 (1996) 76-80.
[28] B.C. Baguley, M. Lebret, Biochemistry, 23 (1984) 937-943.
[29] N. Dharmaraj, P. Viswanathamurthi, K. Natarajan, Transition Met. Chem. 26 (2001)
105-109.
[30] A. Kriza, A. Reiss, S. Florea, T. Caproiu, J. Indian Chem. Soc. 77 (2000) 207-208.
