Synthesis, Characterization and Antifungal Activities of Copper(II) Soaps and their Complexes Derived from Azadirecta Indica (Neem) and Pongamia Pinnata (Karanj) Oil
-
R. Sharma
Abstract
Neem (Azadirecta indica) and Karanj (Pongamia pinnata) oils are ecofriendly, non-toxic, completely biodegradable with antiviral, antifungal, and antibacterial properties. The dark green colour Copper(II) soaps derived from Neem and Karanj oil, their greenish brown complexes with ligand 2-amino-6-methyl benzothiazole containing nitrogen and sulphur have been synthesized and characterized by elemental analysis. IR and NMR of complexes suggest that the complexation has taken place successfully. From the analytical data the stoichiometry of the complexes has been observed to be 1:1 (metal-ligand). Copper soaps and their complexes are good anti-fungal agents. The fungi toxicities of the oils, soaps and complexes of neem and karanj have been investigated. The results indicate that the strain of Candida species is susceptible towards complexes of benzothiazole.
Kurzfassung
Neem (Azadirecta indica) und Karanj (Pongamia pinnata) Öle sind ökologiefreundlich, nichttoxisch und vollständig biologisch abbaubar, mit antiviralen, antifugalen und antibakteriellen Eigenschaften. Die aus Neem- and Karanj-Öl derivatisierten dunkelgrünen Kupfer(II)-Seifen und ihre grünbraunen Komplexe mit stickstoff- und schwefelhaltigen 2-Amino-6-methylbenzothiazol Liganden wurden synthetisiert und durch Elementaranalyse charakterisiert. Die erfolgreich stattgefundene Komplexierung wurde mittels IR und NMR der Komplexe angezeigt. Anhand der analytischen Daten wurde die Stöchiometrie der Komplexe zu 1:1 (Metal-Ligand) bestimmt. Kupfer(II)-Seifen und ihre Komplexe sind gute Antifugalhilfsmittel. Die pilztötende Wirkung der Öle, Seifen und Komplexe von Neem und Karanj wurden untersucht. Die Ergebnisse zeigen, dass die Stammkulturen der Candida-Spezies empfindlich gegenüber Benzothiazolkomlexe sind.
References
1.Swamy, S. J. and Reddy, S. R.: Indian J. Chem40 (A) (2001) (1093).Search in Google Scholar
2.Slegel, S. H. and Martin, R. B.: Chem. Rev.82 (1983) 235.Search in Google Scholar
3.Sherwani, M. R. K., Sharma, R., Gangwal, A. and Bhutra, R.: Indian J. Chem.424 (2003) 2527.Search in Google Scholar
4.Mehta, V. P. and Sharma, R.: Tenside Surf. Det.40 (2) (2003) 99.Search in Google Scholar
5.May, P. M. and Bulman, R. A.: Prog., Med. Chem.20 (1983) 226.Search in Google Scholar
6.Silver, S.: Membrane and Transport Vol. 2, edited by A. N.Martibisum115 (1982) 7.Search in Google Scholar
7.Ojha, K. G., Jaisinghan, N. and Tahiliani, H.: J Indian Chem Soc.79 (2002)191.Search in Google Scholar
8.Pizzi, A.: (Dept. Chem., Witwatersrand, Johannesburg, S. Africa): Holzforschung47 (4), (1993) 343–348.10.1515/hfsg.1993.47.4.343Search in Google Scholar
9.Hirao, C.: (Yamamoto, Isao, Japan), Jpn. Kokai Tokkyo Koho, JP87 (2002) 226.Search in Google Scholar
10.Azam, M., Mohibbe, W. A., Nahar, N. M.: Biomass and Bioenergy29 (2005) 293–302.10.1016/j.biombioe.2005.05.001Search in Google Scholar
11.Matuura, R.: Nippon Kagaku Kaishi82 (1961) 1624.10.1246/nikkashi1948.82.12_1624Search in Google Scholar
12.Barclay, G. A. and Kennard, C. H. L.: J. Indian Chem. Soc.38 (1961) 3289.10.1039/jr9610003289Search in Google Scholar
13.Mehta, V. P., Hasan, M., Mathur, S. P. and Rai, G. L.: Tenside Surf. Det.16 (1979) 2.Search in Google Scholar
14.Manhas, B. S., Kalia, S. B. and Sardana, A. K.: J. Indian Chem. Soc.83 (2006) 652.Search in Google Scholar
15.Reddy, R. K., Reddy, K. M. and Mahendra, K. N.: Indian J. Chem. A45 (2006) 377.Search in Google Scholar
16.Lal, R. A., Basumalary, D., Chakraborty, J., Bhaumik, S. and Kumar, A.: Indian J. Chem. A45 (2006) 619.Search in Google Scholar
17.Patel, R. N., Singh, N. and Gundla, Y. L. N.: Indian J. Chem. A45 (2006) 614.Search in Google Scholar
18.Mijanuddin, M., Gangopathday, S., Mondal, S., Mukharjee, M. and Ali, M.: Indian J. Chem. A45 (2006) 858.Search in Google Scholar
19.Ali, A., Salunke, S., Gawali, Rao, P. and Linares, J.: Indian J. Chem. A45 (2006) 853.Search in Google Scholar
20.Erden, I., Demirhan, N. and Avclata, U.: Indian J. Chem. A45 (2006) 1395.Search in Google Scholar
21.Sharma, V. K. and Shrivastava, S.: Indian J. Chem. A45 (2006) 1368.Search in Google Scholar
22.Basset, J., Denny, R. C., Jeffery, G. H. and Mendham, J.: In Vogel's Textbook of Quantitative Inorganic Analysis, 4th ed., Longman, London (1985).Search in Google Scholar
23.Riddick, J. R. and Bunger, W. B.: Organic Solvents: Physical Properties and Methods of Purification. Wiley Interscience, New York (1970).Search in Google Scholar
24.Gunstone, F. D.: An Introduction to the Chemistry of Fats and Fatty Acids Chapman and Hall Ltd., London (1958).Search in Google Scholar
25.Adams, R.: Organic Reactions John Wiley and sons, New York3 (1959) 240.Search in Google Scholar
26.Sharma, R., Tank, P., Saxena, M., Bhutra, R. and Ojha, K. G.: Tenside Surf. Det.45 (2008) 2, 87–92.Search in Google Scholar
27.Horsfall, G.: Bot: Rev.11 (1945) 357.10.1007/BF02861319Search in Google Scholar
28.Silverstein, R. M., Bassler, G. C. and Morrill, T. C.: “Spectrometric Identification of Organic Compound”. 5th ed.John Wiley and sons Inc. (1991).Search in Google Scholar
29.Yun, D.-S., Hong, J.-H., Lee, W.-Y., Sim, Y.-K. and Lee, K.-H.: (choongwae Pharm. co., S. Korea) Republic Korea KR9, 615, 160 (cl.C11D3/48) 1 Nov. 1996, KR Applications 9, 312, 963, 9 July, 1993.Search in Google Scholar
30.Gunstone, F. D.: The Lipid Handbook, 2nd edition, (1995), pp. 516–519 (Ed: F. D.Gunstone, J. L.Harwood and F. B.Padley, Chapman & Hall, London.Search in Google Scholar
© 2009, Carl Hanser Publisher, Munich
Articles in the same Issue
- Contents/Inhalt
- Contents
- Abstracts
- Abstracts
- Application
- Macroscopic Pipe Flow of Micellar Solutions Investigated by Ultrasound Doppler Velocimetry
- Synthesis, Characterization and Antifungal Activities of Copper(II) Soaps and their Complexes Derived from Azadirecta Indica (Neem) and Pongamia Pinnata (Karanj) Oil
- Synthesis and Properties of Environmentally Friendly Calcium Phosphate Inhibitor
- Basic Science
- Benzene Moiety of Alkylphenol Ethoxylates can be a Source of Π Stacking Interactions
- Novel Surfactants
- O-(2-Hydroxyethyl)cellulose–derived Surfactants Prepared by Microwave–assisted Transesterification
- Physical Chemistry
- The UV Spectroscopic Determination of Two Critical Micelle Concentrations of Domiphen Bromide in Solutions with KBr and Calculations of the Packing Parameter
- Adsorption of CTAB on Zeolite A Detected by Surfactant Ion-selective Electrode
Articles in the same Issue
- Contents/Inhalt
- Contents
- Abstracts
- Abstracts
- Application
- Macroscopic Pipe Flow of Micellar Solutions Investigated by Ultrasound Doppler Velocimetry
- Synthesis, Characterization and Antifungal Activities of Copper(II) Soaps and their Complexes Derived from Azadirecta Indica (Neem) and Pongamia Pinnata (Karanj) Oil
- Synthesis and Properties of Environmentally Friendly Calcium Phosphate Inhibitor
- Basic Science
- Benzene Moiety of Alkylphenol Ethoxylates can be a Source of Π Stacking Interactions
- Novel Surfactants
- O-(2-Hydroxyethyl)cellulose–derived Surfactants Prepared by Microwave–assisted Transesterification
- Physical Chemistry
- The UV Spectroscopic Determination of Two Critical Micelle Concentrations of Domiphen Bromide in Solutions with KBr and Calculations of the Packing Parameter
- Adsorption of CTAB on Zeolite A Detected by Surfactant Ion-selective Electrode