Skip to main content
Log in

Complexes of iron(III) with cyclopropanecarbo- and cyclohexyl-acetohydroxamic acids

  • Full Papers
  • Published:
Transition Metal Chemistry Aims and scope Submit manuscript

Summary

Cyclopropanecarbohydroxamic acid (CPAH) and cyclohexylacetohydroxamic acid (CHAH) were synthesized, characterized and their pK a's determined spectro-photometrically as 9.80 and 9.85, respectively, at 25 °C and in buffers of 0.1 mol dm−3 ionic strength (I). A spectroscopic investigation of their reactions with FeIII in aqueous solutions revealed the sole formation of the 1:3 complexes at equilibrium. Stability constants (log β 3 at 25 °C and I = 0.1 mol dm−3 are 34.80 and 34.22 for [Fe(CPA)3] and [Fe(CHA)3], respectively. Spectral and magnetic studies of the isolated complexes indicate octahedral coordination via the O atoms of the hydroxamate group.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. J. B. Nielands, Structure and Bonding, 1, 59 (1968).

    Google Scholar 

  2. D. A. Brown and M. V. Chidambaram in H. Sigel (Ed.), Metal Ions in Biological Systems, Vol. 14, Dekkar, New York, 1982, p. 125.

    Google Scholar 

  3. H. Kehl, Chemistry and Biology of Hydroxamic Acids, Karger, New York, 1982.

    Google Scholar 

  4. B. Kurzak, H. Kozlowski and F. Farkas, Coord. Chem. Rev., 114, 169 (1992).

    Google Scholar 

  5. J. B. Nielands, Microbial Iron Metabolism, Academic Press, New York, 1974.

    Google Scholar 

  6. J. H. Weisburger and E. K. Weisburger, Pharm. Rev., 25, 1 (1973).

    Google Scholar 

  7. M. Maehr, Pure Appl. Chem., 28, 603 (1971).

    Google Scholar 

  8. T. Emery in H. Sigel (Ed.), Metal Ions in Biological Systems, Vol. 7, Dekkar, New York, 1978, p. 77.

    Google Scholar 

  9. G. W. Bates and P. Saltman in D. R. Williams (Ed.), An Introduction to Bioinorganic Chemistry, Thomas, Illinois, 1972, p. 145.

    Google Scholar 

  10. P. S. Dobbin and R. C. Hider, Chem. Britain, 26, 565 (1990).

    Google Scholar 

  11. W. B. Martin and L. R. Swett, US 2, 928, 875, Chem. Abstr. 54, 15272f (1960).

    Google Scholar 

  12. E. L. Jones and A. W. Scott, J. Am. Chem. Soc., 44, 407 (1922).

    Google Scholar 

  13. A. Albert and E. P. Serjeant, The Determination of Ionization Constants, 2nd Edit., Chapman & Hall, London, 1971, p. 44.

    Google Scholar 

  14. D. D. Perrin, Aust. J. Chem., 16, 572 (1963).

    Google Scholar 

  15. F. R. Hartley, C. Burgess and R. M. Alcock, Solution Equilibria, Ellis Horwood, Sussex, 1980, p. 33.

    Google Scholar 

  16. D. J. Legget and W. A. E. McBryde, Anal. Chem., 41, 1065 (1975).

    Google Scholar 

  17. A. Braibanti and C. Bruschi, Ann. Chim., 67, 471 (1977).

    Google Scholar 

  18. D. J. Legget in D. Legget (Ed.), Computational Methods for the Determination of Stability Constants, Plenum, London, 1985, p. 159.

    Google Scholar 

  19. D. A. Brown, D. McKeith and W. K. Glass, Inorg. Chim. Acta, 35, 5 (1979).

    Google Scholar 

  20. R. L. Dutta and S. Lahiri, J. Indian Chem. Soc., 39, 860 (1962).

    Google Scholar 

  21. B. Chatterjee, J. Indian Chem. Soc., 48, 929 (1971).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Nwabueze, J.N. Complexes of iron(III) with cyclopropanecarbo- and cyclohexyl-acetohydroxamic acids. Transition Met Chem 21, 258–261 (1996). https://doi.org/10.1007/BF00165979

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00165979

Keywords

Navigation