Transition Metal Chemistry

, Volume 35, Issue 6, pp 649–658 | Cite as

Interaction of E. coli DNA with diazine-bridged late first row transition metal complexes derived from hexadentate compartmental ligands: an approach to DNA cleavage/binding studies

Article

Abstract

A series of binuclear CoII, NiII, CuII and ZnII complexes having μ-1,2 diazine bridging have been prepared and characterized by various physico-chemical methods. The hexadentate ligands were synthesized by condensing 3,5-dichloroformyl-1H-pyrazole with 2-hydrazinobenzothiazole (L1H) or 4-aminoantipyrine (L2H) in 1:2 ratio. Gel electrophoresis data indicate cleavage of E. coli DNA to a minute extent by both [Co2L2(μ-Cl)Cl2(H2O)2]·H2O and [Ni2L2(μ-Cl)Cl2(H2O)2]. Conversely, the data for the remaining complexes indicated binding but not cleavage. These results were confirmed by viscosity measurements and absorption spectral studies. An intercalative binding mode is predicted when the title complexes interact with DNA.

Keywords

Pyrazole Antipyrine Benzothiazole Pyrazole Ring TCNE 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Notes

Acknowledgments

The authors thank the USIC and Department of Chemistry, Karnatak University, Dharwad, for providing spectral facility. Recording of FAB mass spectra (CDRI Lucknow) and ESR spectra (IIT Bombay) is gratefully acknowledged. One of the author thanks (Srinivasa Budagumpi) UGC for awarding Research Fellowship in Science for Meritorious Students.

References

  1. 1.
    Parkin G (2004) Chem Rev 104:699CrossRefGoogle Scholar
  2. 2.
    Hobartner C, Silverman SK (2007) Biopolymers 87:279CrossRefGoogle Scholar
  3. 3.
    Morrow JR, Trogler WC (1988) Inorg Chem 27:3387CrossRefGoogle Scholar
  4. 4.
    Morrow JR, Trogler WC (1989) Inorg Chem 28:2330CrossRefGoogle Scholar
  5. 5.
    DeRosch MA, Trogler WC (1990) Inorg Chem 29:2409CrossRefGoogle Scholar
  6. 6.
    Jolley RL, Evans LH, Makino N, Mason HS (1974) J Biol Chem 249:335Google Scholar
  7. 7.
    Fee JA (1975) Struct Bonding (Berlin) 1:23Google Scholar
  8. 8.
    Raman N, Raja JD, Sakhivel A (2007) J Chem Sci 119:303CrossRefGoogle Scholar
  9. 9.
    Xi P-X, Xu Z-H, Liu X-H, Chen F-J, Zeng Z-Z, Zhang X-W, Liu Y (2009) J Fluoresc 19:63CrossRefGoogle Scholar
  10. 10.
    Revankar VK, Arali VH, Mahale VB (1990) Indian J Chem 29A:889Google Scholar
  11. 11.
    Rutavicius A, Iokubaitite S (1984) Khim Geterutsikl Soedin 1:40Google Scholar
  12. 12.
    Vogel AI (1961) A text book of quantitative inorganic analysis, 3rd edn. Longmans Green and Co. Ltd, LondonGoogle Scholar
  13. 13.
    Zhang S, Zhu Y, Tu C, Wei H, Yang Z, Lin L, Ding J, Zhang J, Guo Z (2004) J Inorg Biochem 98:2099CrossRefGoogle Scholar
  14. 14.
    Budagumpi S, Sathisha MP, Kulkarni NV, Kurdekar GS, Revankar VK (2010) J Incl Phenom Macrocycl Chem 66:327CrossRefGoogle Scholar
  15. 15.
    Annigeri SM, Naik AD, Gangadharmath UB, Revankar VK, Mahale VB (2002) Transition Met Chem 27:316CrossRefGoogle Scholar
  16. 16.
    Budagumpi S, Kulkarni NV, Kurdekar GS, Sathisha MP, Revankar VK (2010) Eur J Med Chem 45:455CrossRefGoogle Scholar
  17. 17.
    Saha NC, Saha A, Butcher RJ, Chaudhuri S, Saha N (2002) Inorganica Chim Acta 39:348CrossRefGoogle Scholar
  18. 18.
    Saha NC, Butcher RJ, Chaudhuri S, Saha N (2003) Polyhedron 22:375CrossRefGoogle Scholar
  19. 19.
    Annigeri SM, Sathisha MP, Revankar VK (2007) Transition Met Chem 32:81CrossRefGoogle Scholar
  20. 20.
    Sau DK, Butcher RJ, Chaudhuri S, Saha N (2004) Polyhedron 23:5CrossRefGoogle Scholar
  21. 21.
    Anna KD, El˙zbieta M, Barbara R, Izabela DA, Anna EK, Malgorzata AB (2007) Chem Pharm Bull 55:747CrossRefGoogle Scholar
  22. 22.
    Kalia SB, Lumba K, Kaushal G, Sharma M (2007) Indian J Chem 46A:1233Google Scholar
  23. 23.
    Raman N, Raja SJ, Joseph J, Sakthivel A, Dhaveethu JR (2008) J Chil Chem Soc 53:1599Google Scholar
  24. 24.
    Skorokhod LS, Seifullina II, Vlasenko VG, Pirog IV (2007) Russian J Coord Chem 33:328CrossRefGoogle Scholar
  25. 25.
    Patel RN, Kesharwani MK, Singh A, Patel DK, Choudhary M (2008) Transition Met Chem 33:733CrossRefGoogle Scholar
  26. 26.
    Baligar RS, Revankar VK (2006) J Serb Chem Soc 71:1301CrossRefGoogle Scholar
  27. 27.
    Geary WJ (1971) Coord Chem Rev 7:81CrossRefGoogle Scholar
  28. 28.
    Keshavalu C, Naidu RS, Naidu RR (1985) Polyhedron 4:761CrossRefGoogle Scholar
  29. 29.
    Sathisha MP, Shetty UN, Revankar VK, Pai KSR (2008) Eur J Med Chem 43:2338CrossRefGoogle Scholar
  30. 30.
    Jain MC, Srivastava AK, Jain PC (1977) Inorg Chem Acta 23:199CrossRefGoogle Scholar
  31. 31.
    Polycn DS, Shain I (1966) Anal Chem 38:370CrossRefGoogle Scholar
  32. 32.
    Flanagam JB, Bard AJ, Anson FC (1978) J Am Chem Soc 100:4248CrossRefGoogle Scholar
  33. 33.
    Okawa H, Matsumoto N, Koikawa M, Takeda K, Kida S (1990) Dalton Trans 1353Google Scholar
  34. 34.
    Gomes L, Pereira E, Castro BD (2000) Dalton Trans 1373Google Scholar
  35. 35.
    Gopal M, Shahabuddin MS, Inamdar SR (2002) Proc Indian Acad Sci (Chem Sci) 114:687CrossRefGoogle Scholar
  36. 36.
    Kelly JM, Tossi AB, McConnell DJ, OhUigin C (1985) Nucleic Acids Res 13:6017CrossRefGoogle Scholar
  37. 37.
    Satyanarayana S, Dabroniak JC, Chaires JB (1992) Biochemistry 31:9319CrossRefGoogle Scholar
  38. 38.
    Satyanarayana S, Daborusak JC, Chaires JB (1993) Biochemistry 32:2573CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media B.V. 2010

Authors and Affiliations

  1. 1.Department of ChemistryKarnatak UniversityDharwadIndia

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