PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
Tytuł artykułu

Synthesis, Structural Investigation and Biological Studies of Some Transition Metal Chelates of Acid Hydrazone

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Metal complexes of Ti(III), VO(IV), Cr(III), Mn(III), Fe(III) and Zr(IV) with Schiff base derived from 2-hydroxy-5-methylacetophenone and benzoyl hydrazide have been synthesized and characterized on the basis of elementalanalysis, infrared spectra, magnetic moment, electronic spectra and thermogravimetric studies. Various kinetic parameters evaluated from thermal decomposition data and thermal stabilities of the complexes are also reported. The antibacterial and antifungal activities of 2-hydroxy- 5-methylacetophenone benzoylhydrazone (HMABH) and its complexes have been investigated against various bacterial strains using the disc diffusion technique. All complexes exhibit good biological activity as compared to free ligand. Solid-state electrical conductivity of ligand and its complexes have also been studied over a wide range of temperature and it was found that compounds exhibit semiconucting behavior in the studied range.
Rocznik
Strony
565--571
Opis fizyczny
Bibliogr. 21 poz., rys.
Twórcy
autor
autor
autor
Bibliografia
  • 1. Chopra R.N., Badhwar R.K. and Ghosh S., "Poisonous Plant of India," I.C.A.R., New Delhi, 1965, p. 270.
  • 2. Hirori T, Takahajhi T. and Imamara H., Nippon Mokuzai Gakkaishi, 12, 324 (1966), (Chem. Abstr, 1967, 67, 51047).
  • 3. Craliz J.C., Rub J.C., Willis D. and Edger J., Nature, 35 (1995).
  • 4. Gupta S.S., Shyamraj D., Pal S. and Pal S., Indian J. Chem., 42A, 2352 (2003).
  • 5. Christensen O.T.Z., Anorg. Chem., 27, 325 (1901).
  • 6. Syamal A. and Maurya M.R., Indian J. Chem., 24A, 836 (1985).
  • 7. Tavale S.S. and Gopinathan C, Bull. Chem. Soc. Jpn, 68, 2847 (1995).
  • 8. Maurya M.R. and Gopinathan C, Indian J. Chem., 35A, 701 (1996).
  • 9. Mishra A.P. and.Khare M., J. Indian Chem. Soc, 77, 367 (2000).
  • 10. Reddy K.H. and Reddy M.R., J. Indian Chem. Soc, 79, 219 (2002).
  • 11. Alaudeen M. and Prabhakaran CP., Indian! Chem., 35A, 517 (1996).
  • 12. Mohan M., Gupta N.S., Kumar A. and Kumar M., Inorg. Chim. Acta, 135, 167 (1987).
  • 13. Lai R.A., Pal R.A., Chakraborty J. and Kumar A., Indian J. Chem., 39A, 1194 (2000).
  • 14. Syamal A., Trans. Met. Chem., 11, 235 (1986).
  • 15. Bansod A.D., Aswale S.R., MandlikP.R. and Aswar A.S., J. Nat. Phys. Sci., 19(1) 81 (2005).
  • 16. Aswar A.S., Bansod A.D., Aswale S.R. and Mandlik PR., Indian J. Chem., 43A, 1892 (2004).
  • 17. Casas J.S., Castineiras A., Condori R, Couce M.D., Russo U., Sanchez A., Seoane R. and Sordo J., Poly-hedron, 22, 53 (2003).
  • 18. S/araaJ A. and Kumar D., Indian J. Chem., 23A, 700 (1984).
  • 19. Syamal A. and Gupta B.K., J. Indian Chem. Soc, 8, 911 (1981).
  • 20. Katon J.E. (Ed), "Organic Semiconducting Polymers", Marcel Dekker, New York, 89 (1968).
  • 21. Koca M., Dagdelen F. and Aydogdu Y, Mater. Lett., 58, 2901 (2004).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUJ7-0015-0004
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.