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Effect of pH on the formation of complex compounds with Schiff ...

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<str<strong>on</strong>g>Effect</str<strong>on</strong>g> <str<strong>on</strong>g>of</str<strong>on</strong>g> <str<strong>on</strong>g>pH</str<strong>on</strong>g>....B. M. Kalshetty et al.Pyruic acid Transuminase (SGPT) to normal c<strong>on</strong>diti<strong>on</strong>, and it helps to restore <strong>the</strong> liver functi<strong>on</strong>ing byproviding multidimensi<strong>on</strong>al approach by showing anti-viral, anti-oxidant, anti-inflammatory, immunomodulatory,choleretic and anti-cholestatic activity 8 .The metal <strong>complex</strong>es are still a major line <str<strong>on</strong>g>of</str<strong>on</strong>g> approach to develop new drugs. It involves efforts to combine<strong>the</strong> separate pharmacophoric groups <str<strong>on</strong>g>of</str<strong>on</strong>g> similar activity into <strong>on</strong>e compound. Thus making structural changes in<strong>the</strong> biological activity. As reported earlier <strong>the</strong> thiazolidine ring present in a large number <str<strong>on</strong>g>of</str<strong>on</strong>g> biologically active<strong>compounds</strong> exhibiting different activities. The development <str<strong>on</strong>g>of</str<strong>on</strong>g> penicillin which shows <strong>the</strong> thiozoline ring.The present developments <str<strong>on</strong>g>of</str<strong>on</strong>g> 7-Amino-4-methyl coumarin <strong>compounds</strong> <strong>with</strong> metal i<strong>on</strong>s are most fascinatingand useful areas in medical chemistry. The discovery <str<strong>on</strong>g>of</str<strong>on</strong>g> coumarin as <strong>the</strong>rapeutic agents in 1820’s was <strong>the</strong>beginning <str<strong>on</strong>g>of</str<strong>on</strong>g> <strong>the</strong> coumarin drug development. Due to <strong>the</strong> diversified nature <str<strong>on</strong>g>of</str<strong>on</strong>g> coumarin and is completely safewhich renders as useful substance in drug research.Keeping in view <strong>the</strong> above importance <str<strong>on</strong>g>of</str<strong>on</strong>g> 7-Amino-4methyl coumarin and <strong>the</strong> c<strong>on</strong>tinuati<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> work <strong>on</strong> <strong>the</strong>syn<strong>the</strong>sis <str<strong>on</strong>g>of</str<strong>on</strong>g> <strong>Schiff</strong> base derived from 3-Aldehydosalicylic acid and its <strong>complex</strong> <strong>compounds</strong> <strong>with</strong> metal i<strong>on</strong>ssuch as Cu (II), Zn (II), Ni (II), Co (II), and Cd (II) at different <str<strong>on</strong>g>pH</str<strong>on</strong>g>. The <strong>Schiff</strong> base compound (Scheme 1)syn<strong>the</strong>sized followed by standard procedures 9,10 c<strong>on</strong>tains <strong>the</strong> acidic groups such as –COOH and –OH(phenolic), it is predicted that <strong>the</strong> coordinati<strong>on</strong> behavior <str<strong>on</strong>g>of</str<strong>on</strong>g> ligand would be developed <strong>on</strong> <str<strong>on</strong>g>pH</str<strong>on</strong>g> using differentreacti<strong>on</strong> c<strong>on</strong>diti<strong>on</strong>s and are remarkably different from those reported by Nag et al 11 .,COOHCH 3OHHCNOOScheme-1: <strong>Schiff</strong> base ligand (LH2) 2-hydroxy-3-((4-methyl-2-oxo-2H-chromen-7-ylimino)methyl)benzoic acidResults and Discussi<strong>on</strong><strong>Schiff</strong> base ligands LH 2 (Scheme 1) was syn<strong>the</strong>sized by <strong>the</strong> standard methods 9, 10 . It is dark yellow incolor; it is sparingly soluble in water, in aqueous sodium hydroxide soluti<strong>on</strong>. But, readily soluble in alcohol(owing to <strong>the</strong> possessi<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> <strong>the</strong> phenolic and carboxylic groups).The syn<strong>the</strong>sis <str<strong>on</strong>g>of</str<strong>on</strong>g> coordinati<strong>on</strong> <strong>compounds</strong><strong>with</strong> metal i<strong>on</strong>s at various <str<strong>on</strong>g>pH</str<strong>on</strong>g> ranges reported as follows:(I) At <str<strong>on</strong>g>pH</str<strong>on</strong>g>= 3-4: An aqueous or water-ethanol soluti<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> <strong>the</strong> ligand LH 2 (Scheme 1) reacts <strong>with</strong> metal i<strong>on</strong>s in2:1 molar ratio forming metal <strong>complex</strong> <strong>compounds</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> <strong>the</strong> types [M(LH) 2 ] where M= Cu(II), Zn(II), Cd(II)(Scheme 2) and [M(LH) 2 (OH) 2 ] where M= Co(II), Ni(II) (Scheme 3). The formati<strong>on</strong>s <str<strong>on</strong>g>of</str<strong>on</strong>g> <strong>the</strong> <strong>complex</strong><strong>compounds</strong> at this <str<strong>on</strong>g>pH</str<strong>on</strong>g> range are shown below:MCl 2 (aq) + 2LH 2 (aq)[M (LH) 2 ] + 2 HCl...1Wher as M= Cu (II), Zn (II), Cd (II).andMCl 2 (aq) + 2LH 2 (aq) [M (LH) 2(H 2 O) 2 ]...2wher as M= Co (II), Ni (II).7J. Chem. Bio. Phy. Sci. Sec. A. Nov. 2011- Jan. 2012, Vol.2, N0.1, 6-13

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