Synthesis and Characterization of Some Transition Metal Complexes of Unsymmetrical Tetradentate Schiff Base Ligand
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The solid complexes of Cu(II), Ni(II), Co(II), Mn(II) and Fe(III) with 4-hydroxy-3-(1-{2-(2-hydroxybenzylidene)- amino phenylimino}-ethyl)-6-methy-pyran-2-one (H2L) derived from o-phenylenediamine, 3-acetyl- 6-methyl-(2H) pyran, 2,4 (3H)-dione (dehydroacetic acid or DHA) and salicylic aldehyde have been synthesized and characterized by elemental analysis, conductometry, magnetic susceptibility, UV-visible, IR, 1H-NMR spectra, X-ray diffraction, thermal analysis, and screened for antimicrobial activity. The IR spectral data suggest that the ligand behaves as a dibasic tetradentate ligand with ONNO donor atoms sequence towards central metal ion. From the microanalytical data, the stoichiometry of the complexes has been found to be 1:1 (metal: ligand).The physico-chemical data suggests square planar geometry for Cu(II) and Ni(II) complexes and octahedral geometry for Co(II), Mn(II) and Fe(III) complexes. The x-ray differaction data suggests orthorhombic crystal system for Cu(II) complex, monoclinic crystal system for Ni(II), Co(II) and Fe(III) and tetragonal crystal system for Mn(II) complex. Thermal behaviour (TG/DTA) of the complexes was studied and kinetic parameters were determined by Coats-Redfern method. The ligand and their metal complexes were screened for antibacterial activity against Staphylococcus aureus and Escherichia coli and fungicidal activity against Aspergillus Niger and Trichoderma.
Abstract
The solid complexes of Cu(II), Ni(II), Co(II), Mn(II) and Fe(III) with 4-hydroxy-3-(1-{2-(2-hydroxybenzylidene)- amino phenylimino}-ethyl)-6-methy-pyran-2-one (H2L) derived from o-phenylenediamine, 3-acetyl- 6-methyl-(2H) pyran, 2,4 (3H)-dione (dehydroacetic acid or DHA) and salicylic aldehyde have been synthesized and characterized by elemental analysis, conductometry, magnetic susceptibility, UV-visible, IR, 1H-NMR spectra, X-ray diffraction, thermal analysis, and screened for antimicrobial activity. The IR spectral data suggest that the ligand behaves as a dibasic tetradentate ligand with ONNO donor atoms sequence towards central metal ion. From the microanalytical data, the stoichiometry of the complexes has been found to be 1:1 (metal: ligand).The physico-chemical data suggests square planar geometry for Cu(II) and Ni(II) complexes and octahedral geometry for Co(II), Mn(II) and Fe(III) complexes. The x-ray differaction data suggests orthorhombic crystal system for Cu(II) complex, monoclinic crystal system for Ni(II), Co(II) and Fe(III) and tetragonal crystal system for Mn(II) complex. Thermal behaviour (TG/DTA) of the complexes was studied and kinetic parameters were determined by Coats-Redfern method. The ligand and their metal complexes were screened for antibacterial activity against Staphylococcus aureus and Escherichia coli and fungicidal activity against Aspergillus Niger and Trichoderma.
참고문헌 (37)
- Atkins, R., , Inorg. Chem., 24(127) (1985)
- Yuan,R., , R. Anal. Chem., 65(2572) (1993)
- Ramesh, R., , Synth. React. Inorg. Met-Org. Chem., 26, pp.47~60 (1996)
- Ohashi, Y, , Bull. Chem. Soc. Jpn., 70(1319) (1997)
- Jeong, B.-G., , Bull. Korean Chem. Soc., 17(688) (1996)
- Singh, P, , J. Indian Chem.Soc., 52(958) (1975)
- Mahindru, A., , Nature, 303(64) (1983)
- Patel, P. R., , Indian J. Chem., 38A(563) (1999)
- Phan,N.T.S., , Dalton Trans, 9(1348) (2004)
- Tan, S. F., , Transition Met. Chem., 13, pp.64~68 (1988)
- Marzilli,L.G., , J. Am. Chem. Soc., 93(1374) (1971)
- Jha, N. K., , Synth. React. Inorg. Met-Org.Chem., 14(455) (1984)
- Qayyoom, M. A., , V.Indian J. Chem., 21B(883) (1982)
- Ramarao, N., , Indian J. Chem., 24A(877) (1985)
- Tan, S. F., , TransitionMet. Chem., 9, pp.390~395 (1984)
- Venketeswar, R. P., , Indian J. Chem., 42A(896) (2003)
- Dash, D. C., , J. Indian Chem. Soc., 79, pp.48~50 (2002)
- Natrajan, R., , Transition Met. Chem., 28, pp.29~36 (2003)
- Nakamoto, K, "Infrared Spectra of Inorganic andCoordination Compounds", Wiley Interscience, 159~214 (1970)
- Raman, N, , P.Indian Acad. Sci., 113(3), pp.183~189 (2001)
- Reddy, K. M., , J.Indian Chem. Soc., 17(118) (1994)
- Mokhle,s, , Chinese Chem. Soc., 48, pp.153~158 (2001)
- Lever, A. B. P, "Inorganic Electronic SpectroscopyElsevier", Amsterdam, 275~361
- Satpathy, K.C., , Transition Met. Chem., 16(410) (1991)
- Sacconi, L., , Transition Met. Chem., 61(943) (1968)
- Patel, M. N, , Synth. React. Inorg. Met.Org. Chem., 19(137) (1989)
- Bhave, N, , J. Inorg. Nucl. Chem., 42(977) (1980)
- Revankar, V. K., , Indian J. Chem., 28A(683) (1979)
- Coats, A. W, , Nature, 20(68) (1964)
- El-Awad, A. M, , J. Therm. Anal. Cal., 61(197) (2000)
- Impura,A., , Bull. Chem. Soc.Jpn., 56(2203) (1983)
- Carvajal, J. R, "Graphic Toolfor Powder Diffraction Laborataire leon brillouin (ceal", enrs) 91191 gif suryvette cedex, 2004
- Shoemaker D. P., "Experiments in Physical Chemistry, 5th edn", pp.17~27 (1989), McGraw-Hill International Edition
- Deshmukh M.B, , Indian J. Chem., 44(1659) (2005)
- Mane P. S., , Indian J. Chem., 40(648) (2001)
- Mishra L., , Indian. J. Chem., 32A(446) (1993)
- Dharamraj N, , Natarajan K.Transition Met. Chem, 26(105) (2001)
