PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
Tytuł artykułu

Synthesis, Characterization and Biological Evaluation of 4-Methyl-7-(salicylidineamino)coumarin Metal(II) Complexes

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Four transition M(II) complexes [where M = Cu(II), Zn(II), Cd(II) and Pd(II)] of the organic ligand, 4-methyl-7-(salicylidineamino)coumarin, HL, have been synthesized and characterized by a variety of physicochemical techniques. An octahedral structure is proposed for Cd(II) complex, a tetrahedral structure for the Zn(II) complex while square planar for Pd(II) complex. Thermal decomposition study of the ligand and its metal complexes was monitored by TG and DTG analyses under N2 atmosphere. The decomposition course and steps were analyzed and the activation parameters of the nonisothermal de composition are determined. The negative values of Delta S* indicated the ordered structures of the prepared complexes compared to their starting reactants. The ligand HL and its metal complexes exhibited good antibacterial activities against Escherichia coli and Bacillus subtilis species.
Rocznik
Strony
1745--1755
Opis fizyczny
Bibliogr. 29 poz., rys.
Twórcy
  • Department of Chemistry, Faculty of Science, Alexandria University, P.O. Box 426 Ibrahimia, Alexandria 21321, Egypt Tel: +203 42 700 24, Fax: +203 39 11 794, dr_amelfawzy@ya hoo.com
Bibliografia
  • 1.            Bagihalli G.B., Avaji P.G., Patil S.A. and Badami P.S., Eur. J. Med. Chem., 43, 2639 (2008).
  • 2.            Shebl M., Spectrochim. Acta, Part A, 70, 850 (2007).
  • 3.            Khandar A.A., Hosseini-Yazdi S.A. and Zare S.A., Inorg. Chim. Acta, 358, 3211 (2005).
  • 4.            Chattopadhyay S., Bocelli G., Cantoni A. and Ghosh A., Inorg. Chim. Acta, 359, 4441 (2006).
  • 5.            Egan D., Kennedy R.O., Moran E., Cox D. and Prosser E., Drug Metal. Rev., 22, 503 (1990).
  • 6.            Kostova I., Momekov G., Zaharieva M. and Karaivanova M., Eur. J. Med. Chem., 40, 542 (2005).
  • 7.            Kostova LP., Manolov I. and Radulova M.K., ActaPharm., 54, 37 (2004).
  • 8.            Katyal M. and Singh H.B., Talanta, 15, 1043 (1968).
  • 9.            Bhalla M., Nathani P.K., Bhalla T.N. and Shnker K., J. Indian, Chem., 31(B), 183 (1992).
  • 10.          Deana A., J. Med. Chem., 26, 580 (1983).
  • 11.          Smith R.-E. and Dolbeare F.A., US Patent. 4229528 A (1980).
  • 12.          Aazam E.S., Fawazy A. and Hitchcock P.B., Acta Cryst. E, 62, 4285 (2006).
  • 13.          Aazam E.S., El-Husseiny A.F., Hitchcock P.B. and Alshehri J.M., Cent. Eur. J. Chem., 6, 319 (2008).
  • 14.          Davies D.R. and Webb G.A., Coord. Chem.Rev., 6, 95 (1971).
  • 15.          Gupta K.C., Abdulkadir H.K. and Chand S., J. Mol. Catal. A: Chem., 202, 253 (2003).
  • 16.          Donia A.-M., Al-Boraey H.A. and El-Samalehy M.R, J. Therm. Anal. Calorim., 73, 987 (2003).
  • 17.          El-Bindary A.A., Spectrochim. Acta Part A, 57, 49 (2001).
  • 18.          Zhang Q., Zhai J., Zhang Y., Liu Y. and Wang L., Transit. Metal Chem., 25, 93 (2000).
  • 19.          Nakamoto K., Infrared Spectra of Inorganic and Coordinated Compounds; John Wiley; New York, 1963.
  • 20.          Kachkovski O.D., Tolmachev O.I., Kobryn L.O., Bila E.-E. and Ganushchak M.I., Dyes Pigments, 63, 203 (2004).
  • 21.          Lever A.B.R, Inorganic Electronic Spectroscopy; Elsevier; Amsterdam, 1984.
  • 22.          Gill N.S., Nuttall R.H., Scaife D.E. and Sharp D.A., J. Inorg. Nucl. Chem., 18, 79 (1961).
  • 23.          Refat M.S., EL Kourashy S.A. and Ahmed A.S., J. Mol. Struct., 881, 28 (2008).
  • 24.          Qu L., Sun Y, Chen Y, Yu M. and Peng J., Synth. React. Inorg. Met.-Org. Chem., 24, 1339 (1994).
  • 25.          Coats A.W. and Redfern J.P., Nature, 201, 68 (1964).
  • 26.          Johnson D.W. and Gallagher P.K., J. Phys. Chem., 76, 1474 (1972).
  • 27.          Chohan Z.H., Supuran C.T. and Scozzafava A., J. Enzym Inhib. Med. Chem., 20, 303 (2005) and references therein.
  • 28.          Chohan Z.H., Appl. Organomet. Chem., 20, 112(2005).
  • 29.          Chohan Z.H. and Praveen M., Appl. Organomet. Chem., 15, 617 (2001).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUJ7-0015-0084
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.