Open Access
Subscription Access
Open Access
Subscription Access
Synthesis characterization and antimicrobial activity studies of some transition metal complexes derived from 3-chloro-6-methoxy-N’-((2-thioxo- 1, 2-dihydroquinolin-3-yl) methylene)benzo[b]thiophene-2- carboxyhydrazide
Subscribe/Renew Journal
A series of new coordination complexes of Fe(III), Co(II), Ni(II), and Zn(II), with a new Schiff base 3-chloro-6-methoxy- N'-((2-thioxo-1,2-dihydroquinolin-3-yl)methylene) benzo[b] thiophene-2-carboxyhydrazide have been synthesized and characterized by elemental analysis, UV-Visible, IR spectra, 1HNMR spectra, mass spectra, powder X-ray diffraction data, molar conductance, magnetic susceptibility and TGA. The new Schiff base has been synthesized by the reaction between 3-chloro-6-methoxy benzo[b]thiophene-2-carboxyhydrazide and 2-thioxo-1, 2-dihydroquinoline-3-carbaldehyde. The Schiff base behaves as tridentate ONS donor ligand and forms the complexes of the type ML2-stoichiometry in case of Fe(III), Co(II) and ML-stoichiometry in case of Ni(II), and Zn(II). The Fe(III), Co(II) and Ni(II) complexes have octahedral geometry, whereas Zn(II) complex exhibited square planar geometry. The ligand and its metal complexes have been screened for their antibacterial activity against Staphylococcus aureus and Pseudomonous aeruginosa, antifungal activity against Aspergillus niger and Aspergillus flavus by cup plate method respectively and antioxidant activity by free radical scavenging activity using 1, 1- diphenyl-2-picryl hydrazyl (DPPH), with standard compounds vitamin-C and vitamin-E and DNA cleavage activity.
Keywords
Schiff Base, Metal Complexes And Antimicrobial, Antioxidant Activity And DNA Cleavage Activity
Subscription
Login to verify subscription
User
Font Size
Information
- Topsoe H, Clasen BS, Massoth FE. Hydrotreating Catalysis. Springer-Verlog, Berline. 1996.
- Scherzer J, Gruia AJ. Hydrocracking Science and Technology. Dekker, New York. 1996.
- Benson JW, Schrader GL and Angelici RJ. J. Mol. Cat. 96; 1993: 283.
- Anthony Birri, Jonatham, Steed W, Derek, Tocher A. Polyhedron. 18; 1999: 1825-1833.
- (a) Elderfield RC. In Heterocyclic Compounds. Ed. John Wiley, New York. London. Vol. 4, Chapter 1, p. 1 1960. (b) Wright CW, Addac-Kyereme J, Breen AG, Brown JE, Cox MF, Croft SL, Gokcek Y, Kendrick H, Phillips RM, Pollet PL. J. Med. Chem. 44; 2001: 3187. (c) Sahu NS, Pal C, Mandal NB, Banerjee S, Raha M, Kundu AP, Basu A, Ghosh M, Roy K, Bandyopadhyay S, Bioorg. Med. Chem. 10; 2002:1687. (d) Bringmann G, Reichert Y, Kane V, Tetrahedron. 60; 2004: 3539. (e) Kournetsov VV, Mendez LYV, Gomez CMM, Curr. Org. Chem. 9; 2005: 141.
- Peters W, Richards WHG. Antimalerial Drugs II. Eds Springer- Verlag Berline Heidelberg, New York. Tokyo. 1984.
- (a) Corral RA, Orazi OO, Tetrahedron Lett. 7; 1967: 583. (b) Sekar M, Rajendra Prasad KJ. J. Nat. Prod. 61; 1998: 294. (c) Puricelli L, Innocenti G, Delle Monache G, Caniato R, Filippini R, Cappelletti EM. Nat. Prod. Lett. 16; 2002: 95. (dMarco) JL, Carreiras M C. J. Med. Chem. 6; 2003: 518.
- (a) Pozzo JL, Samat A, Guglielmeth R, Dubest R, Aubard. J. Helv. Chem. Acta. 80; 2004: 725. (b) Ghorab MM, Abdel- Hamide SG, Farrag HA. Acta Pol. Pharm. 58; 2001: 1756. (c) Wang YG, Lin X-F, Cui SU, Synlett. 2004: 1175. (d) Bowman RM, Grundon MF, James KJ, J. Chem. Soc. Perkin Trans 1. 10; 1973: 1055. (e) Morel AF, Larghi EL. Tetrahedron. Asymmetry, 15; 2004: 9.
- Rajiv gupta K, Avinash Gupta, Satya paul and Kachroo PL. Indian J. Chem. 37B; 1998: 1211.
- Sharda Goel and Ritu. Indian J. Heterocyclic Chem. 15; 2006: 401.
- Hirosato Konda, Fumino Sakamoto, Kiyotaka Kawakami and Goro Tsukamoto. J. Med. Chem. 31; 1998: 221.
- William R, Baker, Shaopei Cai, Martin Dimitroff, Liming fang and Joseph H. Therrien. J. Med. Chem. 47; 2004: 4693.
- Pramilla Sah. Indian J. Heterocyclic. Chem. 10; 1998: 13.
- Charles Hall M, Herbert Johnson G and John B Wright. J. Med. Chem. 17; No.7. 1974.
- Abdulqader Alhaidaer A, Atef Abdelkader M and Eric Lein J. J. Med. Chem. 28; 1985: 1394.
- Vetrivel Nadaraj, Senniappan Thamaraj selvi and Raju sasi. Arkivoc. 10; 2006: 82.
- Peter Madrid B, John Sherrill, Ally Liou P, Jennifer Weisman L, Joseph L, DeRisib and Kiplin Guy R. Bio. Org. Med. Chem. Lett. 15; 2005: 1015-1018.
- Vlahov R, Parushev ST, Vlahov J, Nickel P and Snatzke G. Pure and Appl. Chem. 62(7); 1990: 1303.
- Maribel Navarro, Flor Vasquez and Roverto Sanchez –Delgado A. J. Med. Chem. 47; 2004: 5204.
- Pandey VK and Menal Tandon. Indian J. Chem. 40B; 2001: 527.
- Jones DH, Slack R and Wooldridge KRH. J. Org. Chem. 8; 1965: 676.
- Takeuchi Y, Oda T, Chang MR, Okamoto Y, Ono J, Oda Y and Yamato M. Chem. Pharm. Bull. Tokyo. 38(11); 1990: 3048.
- Edmunds Lukevics, Izolda sega, Alla zablotskayn and Skaidrite Germane. Molecules. 2; 1997: 180.
- Yuki Sawada, Hiroshi Kayakiri, Yoshito Abe and Hirokazu Tanaka. J. Med. Chem. 47; 2004: 2853.
- Andrea cappelli, Gal. La pericot Mohr, Andrea Gallelli, Milena Rizzo and Gianluca Giorgi. J. Med. Chem. 47; 2004: 2574.
- Sarah catoen- chackal, Michael facompre, Raymond Houssin and Jean- Pierre Henichart. J. Med. Chem. 47; 2004: 3665.
- Lee BD, Zhanjia Li, Kevin, French Yan Zhaung J and Charles Smith D. J. Med. Chem. 47; 2004: 1413.
- Jaroslaw Polanski, Fatima Zouhiri jenason, Didier Desmacle and marc Le Bret. J. Med. Chem. 54; 2002: 4647.
- Mulwad VV and Dalvi MB. Indian J. Chem. 42B; 2003: 358.
- Heinz H. Pertz and Eckart Eich. J. Med. Chem. 42; 1999: 659.
- Deshmukh MB, Savita Dhongade- Desai and Chavan SS. Indian J. Chem. 44B; 2005:1659.
- Mulwad VV and Lohar MV. Indian J. Chem. 42B; 2003: 1937.
- Singh OMV and Muthukrishnan M. Indian J. Chem. 40B; 2001: 262.
- Guyton AC and Hall JE. The body fluid compartments: extrcellular and intracellular fluids; interstitial fluid and edema. Textbook of medical physiology, 9th ed: Singapore, PA: W. B. Saunders Company, 1998: 306-308.
- Ibrahim Y and Alaaddin C. Transition Met. Chem. 28; 2003: 399.
- Sarkar AR and Mandal S. Synth. React. Inorg. Met. Org. Chem. 30; 2000: 1477.
- Mishra AP and Khare M. J. Indian Chem. Soc. 77; 2000: 367.
- Vogel AI. A Text Book Quantitative Organic Analysis. 3rd Ed. 1962.
- Vilsmeier A & Haack A. Chem. Ber. 60B; 1927: 119.
- Srivastava A & Singh RM. Ind. J. of Chem. Sec-B, 44B; 2005:1868-1875 September.
- Sambrook J, Fritsch EF and Maniatis T. Molecular cloning. A laboratory Manual, 1989: 2nd Edn. Cold Spring Harbor Laboratory. Cold Spring Harbor. New York.
- Tian JL, Gao EQ, Li YT, Liu SX. Synth React. Inorg. Met. Org. Chem. 25; 1995: 417.
- Mahapatra BB, Saraf SK. J. Indian. Chem. Soc. 80; 2003: 696.
- Chandra S, Gupta K. Indian. J. Chem. 40(A); 2001: 775.
- Friggs BN. Introduction to Ligand Fields, John-Wiley and Sons, New York. Interscience Publishers. 1967.
- Chandra S, Gupta LK. Spectrochemica Acta, Parrt A. 60; 2004: 2767.
- Mohamad S, Shakira K.P. Shama and Yasser A. Transition. Metal. Chemistry. 32; 2007: 42-46.
- Jackson GE and Nakani BS. J. Chem. Soc. Dalton. 7; 1996: 1373.
- Geary WJ. Coord. Chem. Rev. 1; 1972: 81.
Abstract Views: 353
PDF Views: 2