PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
Powiadomienia systemowe
  • Sesja wygasła!
  • Sesja wygasła!
  • Sesja wygasła!
Tytuł artykułu

Synthesis and Characterization of First Row Transition Metal Complexes of a Schiff Base Hydrazone Containing Quinoxaline Moiety

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A series of new chromium(III), manganese(II), iron(III), cobalt(II), nickel(II) and copper(II) complexes of the Schiff base hydrazone (HDHAHQO), synthesized from 3-hydrazinoquin oxaline-2-one (HQO) and dehydroacetic acid (DHA) were prepared and characterized. The Schiff base exhibits biambidenticity. It be haves as a monobasic tridentate ONN donor in iron(III) and copper(II) complexes and ONO donor in chromium(III), manganese(II), cobalt(II) and nickel(II) complexes. The nature of bonding and the stereochemistry of the complexes have been deduced from elemental analyses, thermal, infrared, electronic spectra, magnetic susceptibility and conductivity measurements. An octahedral geometry was suggested for all the complexes. The Schiff base ligand, HDHAHQO, and its complexes were tested against one strain Gram+ve bacteria (Staphylococcus aureus), Gram-ve bacteria (Escherichia coli). The prepared metal complexes exhibited higher antibacterial activities than the parent ligand.
Rocznik
Strony
1555--1563
Opis fizyczny
Bibliogr. 46 poz., rys.
Twórcy
  • Department of Chemistry, University College for Women, Osmania University, Koti, Hyderabad – 500095, Andhra Pradesh, India, ananthaprasad2003@yahoo.co.in
Bibliografia
  • 1. Nikam S.S., Cordon J.J., Ortwine D.F., Heimbach T.H., Blackburn A.C., Vartanian M.G., Nelson C.B., Schwarz R.D., Boxer P.A. and Rafferty M.F., J. Med. Chem., 42, 2266 (1999).
  • 2. Auberson Y.P., Bischoff S., Moretti R, Schmutz M. and Veenstra S.J., Bioorg. Med. Chem. Lett., 8, 65 (1998).
  • 3. Auberson Y.P., Acklin P., Allgeier H., Biollaz M., Bischoff S., Ofner S. and Veenstra S.J., Bioorg. Med. Chem. Lett., 8, 71 (1998).
  • 4. Kim K.S., Qian LG., Dickinson K.E.J., Delaney C.L., Bird J.E., Waldron T.L. and Moreland S., Bioorg. Med. Chem. Lett., 39, 2667 (1993).
  • 5. Kim K.S., Qian L.G., Bird J.E., Dickinson K.E.J., Moreland S., Schaeffer T.R., Waldron T.L., Delaney C.L., Weller H.N. and Miller A.V, J. Med. Chem., 36, 2335 (1993).
  • 6. Perez-Melero C, Maya A.B.S., Rey B.D., Pelaez R., Caballero E. and Medarde M., Bioorg. Med. Chem. Lett., 14, 3771 (2004).
  • 7. Piras S., Loriga M. and Paglietti G., // Farmaco, 59, 185 (2004).
  • 8. Corona P., Vitale G., Loriga M. and Paglietti G., Molecules, 11, 998 (2006).
  • 9. Monge A., Palop J.A., de Cerain A.L., Senador V, Martinez-Crespo F.J., Sainz Y, Narro S., Garcia E., de Miguel C, Gonzalez M., Hamilton E., Barker A. J., Clarke E.D. and Greenhow D.T., J. Med. Chem., 38, 1786(1995).
  • 10. Carta A., Loriga M., Zanetti S. and Sechi L.A., II Farmaco, 58, 1251 (2003).
  • 11. Hui X., Desrivot J., Bories C, Loiseau M., FranckX., Hocquemiller R. and Figadere B., Bioorg. Med. Chem. Lett., 16,815 (2006).
  • 12. Li J., Chen J., Zhang V, Wang F., Gui C, Zhang L., Qin Y, Xu Q., Liu H., Nan F., Shen J., Bai D., Chen K., Shen X. and Jiang H., Bioorg. Med. Chem., 14, 5527 (2006).
  • 13. Feng D.Z., Wang M. and Wang B., Polyhedron, 11, 1109 (1992).
  • 14. Feng D.Z., Zhou YK. and Wang B., Polyhedron, 11, 1113 (1992).
  • 15. Rani D.S., Lakshmi P.V.A. and Jayatyagaraju V, Transit. Met. Chem., 19, 75 (1994).
  • 16. Ananthalakshmi P.V., Sandhyarani D. and Jayatyagaraju V, Asian J. Chem., 1, 296 (1995).
  • 17. Sandhyarani D., Jayatyagaraju V. and Ananthalakshmi P.V, Indian J. Chem., 38A, 385 (1999).
  • 18. Anantha Lakshmi P.V, Saritha Reddy P. and Jayatyaga Raju V, Bull. Chem. Soc. Ethiop., 22(3), 385 (2008).
  • 19. Kakemi K., Arita T., Sezaki M. and Kiriyama T., Yakuzaigaku, 18, 77 (1958).
  • 20. Kato Y, Sugrura M. and Yamada H., Gifu Yakka Daigaku Kiyo, 8, 37 (1958).
  • 21. Sistrunk W.A., Food Technol., 11, 336 (1957).
  • 22. Tanaka S., Kolumin Eissei, 25, 138 (1956).
  • 23. Jayabalakrishnan C. and Natarajan K., Synth. React. Inorg. Met.-Org. Chem., 31, 983 (2001).
  • 24. Jeeworth T., Wah H.L.K., Bhowon M.G., Ghoorhoo D. and Babooram K., Synth. React. Inorg. Met.-Org. Chem., 30, 1023 (2000).
  • 25. Dharmaraj N., Viswanalhamurthi P. and Natarajan K., Transit. Metal Chem., 26, 105 (2001).
  • 26. Savanini L., Chiasserini L., Gaeta A. and Pellerano C., Biorg. Med. Chem., 10, 2193 (2002).
  • 27. Ferrari M.B., Capacchi S., Pelosi G., Reffo G., Tarasconi P., Alberlini R., Pinelli S. and Lunghi, Molecules, 12, 1091 (2007).
  • 28. Agarwal R.K., Singh L., Sharma D.K. and Singh R, Turk. J. Chem., 29, 309 (2005).
  • 29. Figgis B.N. and Lewis J., Modern Coordination Chemistry, Interscience Inc., NY, 1960.
  • 30. Philips J., J. Chem. Soc. (C), 2397 (1928).
  • 31. Cheeseman G.W.H. and Rafiq M., J. Chem. Soc. (C), 453 (1971).
  • 32. Abdulla A.K. and Ismail K.Z., Can. J. Chem., 72, 1785 (1994).
  • 33. Sama B.D. and Bailer J.C., J. Am. Chem. Soc, 11, 5476 (1955).
  • 34. Sengupta S.K., Pandey O.P., Pandey J.K. and Pandey G.K., Indian J. Chem. A, 40(8), 887 (2001).
  • 35. Shrivastava V., Shrivastava S.K. and Mishra A.P., Proc. Ind. Acad. Sci. A, 65, 247 (1995).
  • 36. Ochocki J., Zurowska B., Mrozinski J., Kooijman H., Spek A.L. and Reedijk J., Eur. J. Inorg. Chem., 169 (1998).
  • 37. Mishra A.P. and Pandey L.R., Indian J. Chem. A, 44(1), 94 ( 2005).
  • 38. Raman N, Ravichandran S. and Thangaraja C, J. Chem. Sci. India, 116(4), 215 (2004).
  • 39. NejatiK. and Rezvani Z., .J. Chem., 27(11), 1665 (2003).
  • 40. Maurya M.R., Khurana S., Schulzke C. and Rehder D., Eur. J. Inorg. Chem., 779 (2001).
  • 41. Getova V.T., PantchevaI.N., Ivanov D.S., MehandjievD.R., Skumryev V. andBontchevP.R., Cent. Eur. J. Chem., 5, 118 (2007).
  • 42. Lider E.V., Russ. J. Coord. Chem., 33, 37 (2007).
  • 43. Revanasiddappa M., Suresh T., Khasim S., Raghavendra S.C., Basavaraja C. and Angadi S.D., E-J. Chem., 5(2), 395 (2008).
  • 44. Figgis B.N., Introduction to Ligand Field, Wiley, NY, 1966.
  • 45. Lever A.B.P., Inorganic Electronic Spectroscopy, 2nd Ed., Elsevier, Amsterdam, 1984.
  • 46. Rehder D., Inorg Chem. Comm., 6(5), 604 (2003).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUJ7-0015-0064
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.