National Academy of Agricultural Sciences (NAAS)
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PRINT ISSN : 2319-7692
Online ISSN : 2319-7706 Issues : 12 per year Publisher : Excellent Publishers Email : editorijcmas@gmail.com / submit@ijcmas.com Editor-in-chief: Dr.M.Prakash Index Copernicus ICV 2018: 95.39 NAAS RATING 2020: 5.38 |
Semicarbazones are compounds which are synthesized by condensation of semicarbazide hydrochloride and aldehydes or ketones. The literature survey revealed that semicarbazones had been emerged as a compound with broad range of activities including anticonvulsant, antitubercular, anticancer and antimicrobial activity. The aim of this study is to synthesis and characterization of 4-Hydroxy-3-methoxybenzaldehyde seimcarbazone Schiff base and its Nickel (II), Cobalt (II) complexes and 2-Hydroxy-5-nitrobenzaldehyde seimcarbazone Schiff base and its Nickel (II) complex. The results of FT-IR and UV-Vis spectra of the Schiff bases and metal complexes confirm the formation of azomethine group (C=N) accompanied with the absence of carbonyl group and the formation of new (M-N) and (M-O) bonds with all metal ions. The results assign that 4-Hydroxy-3-methoxybenzaldehyde seimcarbazone is neutral and bidentate species witch coordinated via azomethine N and O with both metal ions and 2-Hydroxy-3-methoxybenzaldehyde seimcarbazone is neutral tridentate species witch coordinated via azomethine N, O and OH group. The antimicrobial activity of Schiff bases and their metal complexes was carried out against four types of bacteria (Bacillus subtilis, Pseudomonas aeruginosa, Staphylococcus aureus and Escherichia coli) and one fungus (Candida ablicans) by using disc diffusion method. The results showed that the two Schiff bases were active against four tested organisms. The Nickel (II) complex of 4-Hydroxy-3-methoxybenzaldehyde seimcarbazone was active against one type of bacteria (Pseudomonas aeruginosa) and partially active against three type of bacteria (Escherichia coli, Staphylococcus aureus and Bacillus subtilis) and one fungus (Candida albicans) and Cobalt (II) complex of 4-Hydroxy-3-methoxybenzaldehyde seimcarbazone was partially active against one type of bacteria (Staphylococcus aureus) and one fungus (Candida albicans) and inactive against three type of bacteria (Escherichia coli, Pseudomonas aeruginos and Bacillus subtilis). And Nickel (II) complex of 2-Hydroxy-5-nitrobenzaldehyde seimcarbazone was partially active against two type of bacteria (Escherichia coli, Pseudomonas aeruginos) and one fungus (Candida albicans) and inactive against two type of bacteria (Pseudomonas aeruginosa and Bacillus subtilis).
Abou-Mehla, K.S. and Faruk, H. (2008). Bimetallic Complexes of Schiff Base Bis-[4-Hydroxycoumarin-3-yl]-1N,5N-Thiocarbohydrazone as a Potentially Dibasic Pentadentate Ligand. Synthesis, Spectral and Antimicrobial Properties. Journal of the Iranian Chemical Society, 5, 122-134. http://dx.doi.org/10.1007/BF03245825
Aliyu, H.N, H.J Abdullahi (2009). Synthesis and characterization of divalent metal complexes of N, Nbis(Benzoin)-o-phenylenediiminato complexes. African Scientist, Vol. 10, pp. 199-202.
Deligonul, N., M. Tumer, S. Serin, (2006). Synthesis and Characterization, Catalytic, Electrochemical and Thermal Properties of Tetradentade Schiff Base Complexes, Trans. Met. Chem. Vol.31, pp. 920-929 http://dx.doi.org/10.1007/s11243-006-0087-0
Eman Ali Atiyah and Enaam Ismail Yousif (2024). New Semicarbazone Schiff Base Coordination; Synthesis, Characterization and Biological Evaluation. Wasit Journal for Pure Science. 3(1). 333-344. http://dx.doi.org/10.31185/wjps.367
Grunwald, K.R., G. Saischek, M. Volpe, F. Belaj, N.C. Mosch Zanetti, (2010). Pyridazine-Based Ligands and Their Coordinating Ability towards First-Row Transition Metals, Eur. J. Inorg. Chem. Vol.15, pp.2297-2305
Ibrahim, M.N., S.E.A. Sharif, (2007). Synthesis, characterization and use of Schiff Bases as fluorimetric analytical reagents. E-J. Chem., Vol. 4, pp.531-535.
Kumar, S., D.N. Dhar, P.N. Saxena (2009). Applications of metal complexes of Schiff bases: a review. J. Sci. Ind. Res., Vol. 68, pp. 181-187.
Lobana, T.S., Sharma, R., Bawa, G. and Khanna, S. (2009). Bonding and Structure Trends of Thiosemicarbazone Derivatives of MetalsAn Overview. Coordination Chemistry Reviews, 253, 977-1055. http://dx.doi.org/10.1016/j.ccr.2008.07.004
Mar?´a C. Rodr?´guez-Argu¨elles, Estefania C. Lo´pez-Silva a, Jesu´s Sanmart?´n, P. Pelagatti c , Franca Zani (2005). Copper complexes of imidazole-2-, pyrrole-2- and indol-3-carbaldehyde thiosemicarbazones: Inhibitory activity against fungi and bacteria. Journal of Inorganic Biochemistry 99 (2005) 2231-2239 https://doi.org/10.1016/j.jinorgbio.2005.07.018
Mohammadi H. Khan, M. Salehifard, M.H. Abnosi, (2009). Synthesis, Characterization, biological and thermal Studies of Cu(II) complexes of Salen and tetrahedrosalen ligands. J. Iran. Chem. Soc., Vol. 6, pp. 300-309. https://doi.org/10.1007/BF03245838
Naeimi, H., J. Safari, A. Heidarnezhad, (2007). Synthesis of Schiff base ligands derived from condensation of salicylaldehyde derivatives and synthetic diamine. Dyes and Pigments, Vol. 73, pp. 251-253. https://doi.org/10.1016/j.dyepig.2005.12.009
National Committee for Clinical Laboratory Standards (NCCLS) (1999). Performance standards for antimicrobial susceptibility testing; ninth informational supplement. Wayne, Pensilvania document M100-S9, Vol(19).
Singh, D. P., Krishan Kumar, Saurabh Sudha Dhiman, Jitender Sharma (2009). Biologically active macrocyclic complexes derived from diaminonaphthalene and glyoxal: Template synthesis and spectroscopic approach. 24(3), 795-803 https://doi.org/10.1080/14756360802397179
Sun, S., C.L Stern, S. T. Nguyen, J.T Hupp, (2004). Directed assembly of transition-metal-coordinated molecular loops and squares from salen-type components. Examples of metallation-controlled structural conversion. J. Am. Chem. Soc., Vol. 126, pp. 6314-6326. https://doi.org/10.1021/ja037378s
Tokunaga, M., J.F Larrow, F. Kakiuchi, E.N. Jacobsen, (1997). Asymmetric catalysis with water: efficient kinetic resolution of terminal epoxides by means of catalytic hydrolysis. Science, Vol. 277, pp. 936-938. https://doi.org/10.1126/science.277.5328.936
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