Synthesis, characterization and antimicrobial activity of 3d transition metal complexes of a biambidentate ligand containing quinoxaline moiety

Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy

Volumn 74, Issue 1, 2009, Pages 52-57

  Anantha Lakshmi, P V ^a   Reddy, P Saritha ^a   Raju, V Jayatyaga ^b  

^a OSMANIA UNIVERSITY   (India)

^b ADDIS ABABA UNIVERSITY   (Ethiopia)

Author keywords

Antimicrobial activity; Bis bidentate donor; Octahedral geometry; Subnormal magnetic moments

Indexed keywords

3D TRANSITION METALS; ANTIMICROBIAL ACTIVITY; BIS BIDENTATE DONOR; CONDUCTIVITY MEASUREMENTS; COPPER COMPLEXES; ELECTRONIC SPECTRUM; ELEMENTAL ANALYSIS; NEW SERIES; NICKEL COMPLEX; OCTAHEDRAL GEOMETRY; OXOVANADIUM; QUINOXALINES; STAPHYLOCOCCUS AUREUS; SUBNORMAL MAGNETIC MOMENTS;

BACTERIOLOGY; CHELATION; CHROMIUM; CHROMIUM COMPOUNDS; COBALT; COBALT COMPOUNDS; COMPUTATIONAL GEOMETRY; COPPER COMPOUNDS; ESCHERICHIA COLI; LIGANDS; MAGNETIC MOMENTS; MAGNETIC SUSCEPTIBILITY; MANGANESE; METAL COMPLEXES; NICKEL ALLOYS; NICKEL COMPOUNDS; STEREOCHEMISTRY; VANADIUM COMPOUNDS;

IRON COMPOUNDS;

ANTIINFECTIVE AGENT; CHROMIUM; COBALT; COPPER; IRON; LIGAND; MANGANESE; METAL; NICKEL; OXOVANADIUM IV; QUINOXALINE DERIVATIVE; VANADIC ACID;

ARTICLE; CHEMISTRY; DRUG EFFECT; ESCHERICHIA COLI; MACROMOLECULE; MICROBIOLOGICAL EXAMINATION; PHYSIOLOGY; STAPHYLOCOCCUS AUREUS; SYNTHESIS;

ANTI-INFECTIVE AGENTS; CHROMIUM; COBALT; COPPER; ESCHERICHIA COLI; IRON; LIGANDS; MACROMOLECULAR SUBSTANCES; MANGANESE; METALS; MICROBIAL SENSITIVITY TESTS; NICKEL; QUINOXALINES; STAPHYLOCOCCUS AUREUS; VANADATES;

EID: 68849087190     PISSN: 13861425     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.saa.2009.05.007     Document Type: Article

References (42)

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 (1999) 2266
2. Auberson Y.P., Bischoff S., Moretti R., Schmutz M., and Veenstra S.J. Bioorg. Med. Chem. Lett. 8 (1998) 65
3. Auberson Y.P., Acklin P., Allgeier H., Biollaz M., Bischoff S., Ofner S., and Veenstra S.J. Bioorg. Med. Chem. Lett. 8 (1998) 71
4. Kim K.S., Qian L.G., Dickinson K.E.J., Delaney C.L., Bird J.E., Waldron T.L., and Moreland S. Bioorg. Med. Chem. Lett. 39 (1993) 2667
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 (1993) 2335
6. Perez-Melero C., Maya A.B.S., Rey B.D., Pelaez R., Caballero E., and Medarde M. Bioorg. Med. Chem. Lett. 14 (2004) 3771
7. Piras S., Loriga M., and Paglietti G. Il Farmaco 59 (2004) 185
8. Corona P., Vitale G., Loriga M., and Paglietti G. Molecules 11 (2006) 998
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 (1995) 1786
10. Carta A., Loriga M., Zanetti S., and Sechi L.A. Il Farmaco 58 (2003) 1251
11. Hui X., Desrivot J., Bories C., Loiseau P.M., Franck X., Hocquemiller R., and Figadere B. Bioorg. Med. Chem. Lett. 16 (2006) 815
12. Li J., Chen J., Zhang L., 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 (2006) 5527
13. Dianzhong F., Wang M., and Wang B. Polyhedron 11 (1992) 1109
14. Dianzhong F., Yukin Z., and Wang V. Polyhedron 11 (1992) 1113
15. Billing D.E., Underhill A.E., Adams D.M., and Morris D.M. J. Chem. Soc. (1966) 902
16. Xu Z., and Wang M. Spectrochim. Acta A: Mol. Biomol. Spectrosc. 19 3 (1999) 330
17. Rani D.S., Lakshmi P.V.A., and Jayatyagaraju V. Trans. Met. Chem. 19 (1994) 75
18. Ananthalakshmi P.V., Sandhyarani D., and Jayatyagaraju V. Asian J. Chem. 7 (1995) 296
19. Sandhyarani D., Jayatyagaraju V., and Ananthalakshmi P.V. Indian J. Chem. 38A (1999) 385
20. Lakshmi P.V.A., Reddy P.S., and Raju V.J. Bull. Chem. Soc. Ethiop. 22 3 (2008) 385
21. Figgis B.N., and Lewis J. Modern Coordination Chemistry (1960), Interscience Inc., New York
22. Philips J. Chem. Soc. (C) (1928) 2397
23. Cheeseman G.W.H., and Rafiq M. J. Chem. Soc. (C) (1971) 453
24. Lin S.-K. Molecules 1 (1996) 37
25. Angelici R.J. Synthesis and Technique in Inorganic Chemistry (1969), Saunders, Philadelphia
26. Ayman H.A., Ahmed A.O., and Gamal M.E. J. Appl. Sci. Res. 2 1 (2006) 44
27. Melha K.S.A. Spectrochim. Acta A: Mol. Biomol. Spectrosc. 70 (2008) 162
28. Boghaei M.D., and Lashanizadagan M. Synth. React. Inorg. Met. -Org. Chem. 30 (2000) 1393
29. Sengupta S.K., Pandey O.P., Srivastava B.K., and Sharma V.K. Trans. Met. Chem. 23 (1998) 349
30. Abou-Melha K.S., and Faruk H. J. Iran. Chem. Soc. 5 1 (2008) 122
31. Elzahany E.A., Hegab K.H., Khalil S.K.H., and Youssef N.S. Aust. J. Basic Appl. Sci. 2 2 (2008) 210
32. Braibanti A., Dallavalle F., Pellinghelli M.A., and Leporati E. Inorg. Chem. 7 (1968) 1430
33. Day K., and Bandhyopadhyay D. Indian J. Chem. 31A (1992) 37
34. Agarwal R.K., Singh L., Sharma D.K., and Singh R. Turk. J. Chem. 29 (2005) 309
35. Nakamoto K. Infrared and Raman Spectra of Inorganic and Coordination Compounds. 3rd ed. (1997), Wiley, New York
36. Cezar S., Maria P., and Cristian T. Turk. J. Chem. 32 (2008) 487
37. Kato M., Jonassen B., Fanning J.C., and Cusachs L.C. Chem. Rev. 64 (1964) 99
38. Reddy P.S., Susheela T., and Tyagaraju V.J. Ind. Chem. J. 43A (2004) 341
39. Dharamraj N., Viswanathamurthi P., and Natrajan K. Trans. Met. Chem. 26 (2001) 105
40. Tweedy B.G. Phytopathology 55 (1964) 910
41. Ankri S., Miron T., Rabonkov A., Wilchek M., and Mirelman D. Antimicrob. Agents Chemother. 41 (1997) 2286
42. Tortora G.J., Funka B.R., and Case C.L. Microbiology-An Introduction. 6th ed. (1998), Addison Wesley Longman Inc.