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

Kumar, K.; Santhi, N.

doi:10.18052/www.scipress.com/ILCPA.8.46

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

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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:

February 2013

Authors:

K. Kumar, N. Santhi

Keywords:

Antibacterial, Antifungal Activity, Complexes, Metals, Substituted Benzaldehyde

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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).

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