Subscribe

Subscribe to our Newsletter and get informed about new publication regulary and special discounts for subscribers!

ILCPA > Volume 8 > Synthesis, Complexation, Spectral and...
Synthesis, Complexation, Spectral and Antimicrobial Study of Some Novel 5-Bromo-2-Fluorobenzaldehydeoxime
< Back to Volume

Synthesis, Complexation, Spectral and Antimicrobial Study of Some Novel 5-Bromo-2-Fluorobenzaldehydeoxime

Full Text PDF

Abstract:

In this newly approached method a novel series of Transition metal complexes were synthesized by the reaction of 5-bromo-2-fluorobenzaldehyde (1) react with hydroxylamine in ethanolic solution at room temperature. Mononuclear complexes were synthesized by reaction with Cu(II), Zn(II) and Hg(II) chloride salts. The complexes were characterized by elemental analysis, Ultraviolet, Infrared and 1HNMR spectral studies. The antimicrobial activities of the ligand and its metal complexes were estimated.

Info:

Periodical:
International Letters of Chemistry, Physics and Astronomy (Volume 8)
Pages:
46-52
DOI:
https://doi.org/10.18052/www.scipress.com/ILCPA.8.46
Citation:
K. Kumar and N. Santhi, "Synthesis, Complexation, Spectral and Antimicrobial Study of Some Novel 5-Bromo-2-Fluorobenzaldehydeoxime", International Letters of Chemistry, Physics and Astronomy, Vol. 8, pp. 46-52, 2013
Online since:
September 2013
Authors:
K. Kumar, N. Santhi
Keywords:
Antibacterial, Antifungal Activity, Complexes, Metals, Substituted Benzaldehyde
Export:
RIS, BibTeX, Text
Distribution:
Open Access

Creative Commons License
This work is licensed under a
Creative Commons Attribution 4.0 International License

References:

[1] Desai J. J., Desai P. G., Mehta A. G., Asian J Chem. 11 (1999) 519.

[2] Desai J. J., Desai P. G., Mehta A. G., Asian J Chem. 12 (2000) 1067.

[3] Hania M. M., Asian J Chem. 14 (2002) 1074.

[4] Rai B. K., Asian J Chem. 14 (2002) 1595.

[5] Rai B. K., Asian J Chem. 14 (2002) 312.

[6] Hania M. M., Asian J Chem. 17 (2005) 439.

[7] Dobeck A. S., Klayman D., Antimicrob Agents Chemother. 18 (1980) 27.

[8] Wagner W. H., Winkelman E., Arzneim Forschi 22 (1972) 1713.

[9] Hania M. M., Asian J Chem. 17 (2007) 439.

[10] Morrison N. E., Collins F. M, Int J Leprosy 49 (1981) 180.

[11] Jones D. H., Slack R., Squires S., J Med Chem. 2 (1965) 676.

[12] Klayman D. L., Joseph F., J Med Chem., 22 (1979) 855.

[13] Bauer D. J., Vincent L. S., Kempe C. H., Dowine A. W., Lancet, 2 (1963) 494.

[14] Petering H. G., Buskik H. H., Underwood G. E., Cancer Res. 64 ( 1963) 367.

[15] K. Krishnankutty, M. B. Ummathur, P. Ummer, J. Serb. Chem. Soc. 74 (2009) 1273.

[16] Rana A. K., Shah J. R., Indian J Chem. 20A (1981) 142.

[17] M. Kurtoğlu, E. Ispir, N. Kurtoğlu, S. Serin, Dyes Pigm. 77 (2008) 75.

[18] R. M. Silverstein, G. C. Bassler, T. C. Morrill., Spectrometric Identification of Organic Compounds, 5th ed., Wiley, New York, (1991).

Show More Hide