Transition Metal Chemistry

, Volume 30, Issue 6, pp 765–770 | Cite as

New Soluble Coordination Chain Polymers of Nickel(II) and Copper(II) ions and their Biological Activity

  • Mükerrem Kurtoğlu
  • Esin İspir
  • Nurcan Kurtoğlu
  • Sevil Toroğlu
  • Selahattin Serin
Article

Abstract

A new tetraoxime ligand, (2E, 3E, 9E, 10E)-1, 4, 8, 11-tetraazacyclotetradecane-2, 3, 9, 10-tetrone tetraoxime has been prepared by the template condensation of 1,3-propanediamine and cyanogen-di-N-oxide, obtained by treating (E, E)-dichloroglyoxime in CH2Cl2 with Na2CO3 at −10 °C. The coordination chain polymers {[(pnngH2)2Ni]n (5) and [(pncgH2)2Cu]n(6)} of two transition metal ions, [Ni(II) and Cu(II)] with the vic-dioxime ligand have been prepared. The oxime ligand acts as a polydentate ligand bending through nitrogen atoms in the presence of a base, as do most of the vic-dioximes. In the complexes, the chloride ions coordinate to the nickel and copper ions. The structures of these novel vic-dioxime compounds are proposed on the basis of the elemental analyses, molar conductance data, i.r., and U.v.–visible are presented. Elemental analyses indicate a ligand metal ratio of 1:1 in the coordination polymers. Conductivity measurements have shown that mono- and polynuclear complexes are non-electrolytes. In addition, anti-microbial activities of the compounds have been investigated.

Keywords

CH2Cl2 Nitrogen Atom Oxime Coordination Polymer Conductance Data 
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.

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. 1.
    Rivas, B.L., Pereira, E.D., Moreno-Villoslada, I. 2003Prog. in Polym. Sci28173CrossRefGoogle Scholar
  2. 2.
    Tsuchida, E., Nishide, H. 1977Adv Polym Sci241Google Scholar
  3. 3.
    Higashi, F., Cho, C.S., Hinoki, H. 1979J Polym Sci Polym Chem Ed17313CrossRefGoogle Scholar
  4. 4.
    Buchmeiser, M.R., Kröll, R., Wurst, K., Schareina, T., Kempe, R. 2001Macromol Symp164187CrossRefGoogle Scholar
  5. 5.
    Michalska, Z.M., Strzelec, K., Sobczak, J.W. 2000J. Mol. Catal. A␣Chem15691CrossRefGoogle Scholar
  6. 6.
    Akelah, A., Moet, A. 1990Functionalized Polymers and Their ApplicationsChapman & HallLondonGoogle Scholar
  7. 7.
    Breslow, R., Belvedere, S., Gershell, L., Leung, D. 2000Pure Appl. Chem72333Google Scholar
  8. 8.
    Hojo, N., Shirakai, H., Hayashi, S. 1974J. Polym. Sci. Polym. Symp47299Google Scholar
  9. 9.
    Travers, C., Marinsky, J.A. 1974J. Polym. Sci. Polym. Symp47285Google Scholar
  10. 10.
    Chiang, W.Y., Mei, W.P. 1993Eur. Polym. J291047CrossRefGoogle Scholar
  11. 11.
    Durmuş, M., Ahsen, V., Luneau, D., Pécaut, J. 2004Inorg. Chim. Acta357588CrossRefGoogle Scholar
  12. 12.
    Kantekin, H., Ocak, Ü., Gök, Y., Alp, H. 2002Polyhedron211865CrossRefGoogle Scholar
  13. 13.
    Kurtoglu, M., Serin, S. 2002Synth. React. Inorg. Met.-Org. Chem32629CrossRefGoogle Scholar
  14. 14.
    Kurtoglu, M., Serin, S. 2001Synth. React. Inorg. Met.-Org. Chem311129CrossRefGoogle Scholar
  15. 15.
    Kurtoğlu, N., Kurtoğlu, M., Serin, S. 1999Synth. React. Inorg. Met- Org. Chem291779Google Scholar
  16. 16.
    Kandaz, M., Yı ılmaz, İ., Keskin, S., Koca, A. 2002Polyhedron21825CrossRefGoogle Scholar
  17. 17.
    Melson, G.A. 1979Co-ordination Chemistry of Macrocyclic CompoundsPlenum PressNew YorkCh. 2Google Scholar
  18. 18.
    Dilworth, J.R., Parrott, S.J. 1998Chem. Soc. Rev2743CrossRefGoogle Scholar
  19. 19.
    Blower, P.J. 1998Transition Met. Chem23109CrossRefGoogle Scholar
  20. 20.
    Wolkert, W.A., Hoffman, T.J. 1999Chem. Rev992269CrossRefPubMedGoogle Scholar
  21. 21.
    Ohta, K., Higashi, R., Ikejima, M., Yamamoto, I., Kobayashi, N. 1998J. Mater. Chem81979CrossRefGoogle Scholar
  22. 22.
    Malmstrom, B.G. 1993Acc. Chem. Res26332CrossRefGoogle Scholar
  23. 23.
    Laranleira, M.C.M., Marusak, R.A., Lappin, A.G. 2000Inorg. Chim. Acta186300Google Scholar
  24. 24.
    Bakir, M. 1999J. Electroanal. Chem46660CrossRefGoogle Scholar
  25. 25.
    M. Bakir, J.A.M. McKenzie J. Chem. Soc., Dalton Trans. 3571 (1997)Google Scholar
  26. 26.
    Birbiçer, N., Kurtoğlu, M., Serin, S. 1999Synth. React. Inorg. Met.-Org. Chem291353Google Scholar
  27. 27.
    (a)G. Ponzio, F. Baldroco, Gazz. Chim. Ital., 60, 415 (1930); (b) H. Brintzinger, R. Titzmann, Chem. Ber., 85, 344 (1952).Google Scholar
  28. 28.
    Attia, A.S., El-Mashtouly, S.F., El-Shahat, M.F. 2002Synth. React. Inorg. Met.-Org. Chem32509CrossRefGoogle Scholar
  29. 29.
    Kurtoğlu, M. 2004Synth. React. Inorg. Met.-Org. Chem34967CrossRefGoogle Scholar
  30. 30.
    Kurtoglu, M., Serin, S. 2001Synth. React. Inorg. Met.-Org. Chem311229CrossRefGoogle Scholar
  31. 31.
    Kandaz, M., Koca, A., R Özkaya, A. 2004Polyhedron231987CrossRefGoogle Scholar
  32. 32.
    C.H. Collins, P.M. Lyne, Microbial Methods, University park Press, Baltimore, 422 (1970).Google Scholar
  33. 33.
    Sengupta, S.K., Pandey, O.P., Srivastava, B.K., Sharma, V.K. 1998Transition Met. Chem23349CrossRefGoogle Scholar

Copyright information

© Springer 2005

Authors and Affiliations

  • Mükerrem Kurtoğlu
    • 1
  • Esin İspir
    • 1
  • Nurcan Kurtoğlu
    • 2
  • Sevil Toroğlu
    • 3
  • Selahattin Serin
    • 4
  1. 1.Department of ChemistryKahramanmaraş Sütçü İmam UniversityK. MaraşTurkey
  2. 2.Engeenering FacultyKahramanmaraş Sütçü İmam UniversityK. MaraşTurkey
  3. 3.Department of BiologyKahramanmaraş Sütçü İmam UniversityK. MaraşTurkey
  4. 4.Department of ChemistryÇukurova UniversityAdanaTurkey

Personalised recommendations