Synthesis and Biological Activity of Novel Azomethine Compounds
KrishiKosh
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Title |
Synthesis and Biological Activity of Novel Azomethine Compounds
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Creator |
Tilak Mondal
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Contributor |
Rajesh Kumar
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Subject |
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Description |
T-8488
Schiff bases are well known for their wide spectrum of biological activities. Recently, Schiff bases have been discovered as excellent fungicide and nitrification inhibitor. To optimize the structure to improve the bioactivity of azomethine (Schiff Base) derivatives, 23 novel Schiff bases derived from 2,4,5-trichloroaniline were synthesized and characterized using spectral techniques. These molecules were further explored for their antifungal activity against Rhizoctonia bataticola and Sclerotium rolfsii and nitrification inhibitory activity under laboratory conditions. For the nitrification inhibition, compounds were tested at three doses (1, 5 and 10%) along with reference inhibitors, N-Serve, Dicyandiamide and urea for 28 days incubation period. Significantly higher ammonium-N and less nitrate-N were observed with all title compounds as compared to urea alone. No nitrite-N was observed in all the treatments. All test compounds were highly effective as nitrification inhibitors. The potent compounds emerged from the series were (2,4-dimethoxybenzylidene)-(2,4,5-trichlorophenyl)-amine (C23) (4-isopropylbenzylidene)-(2,4,5-trichlorophenyl)-amine (C21) and (3,4,5- trimethoxybenzylidene)-(2,4,5-trichlorophenyl) amine (C3). In case of antifungal activity all test compounds were highly effective against both the pathogenic fungi except (2- nitrobenzylidine)-(2,4,5-trichlorophenyl) amine. In general, test compounds were more effective against R. bataticola (ED50, 9.4-66.2 μg/ml) as compared to S. rolfsii (ED50, 10.6-117.1 μg/ml). The maximum antifungal activity was observed with compound, (3,4,5-trimethoxybenzylidine)-(2,4,5-trichlorophenyl) amine (C3) with ED50 9.4 μg/ml against R. Bataticola. On the other hand, (4-tert-butyl-benzylidine)-(2,4,5- trichlorophenyl)-amine (C-15) was best against S. rolfsii with ED50, 10.6 μg/ml with high unit activity against R. bataticola also (ED50, 11.4 μg/ml). |
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Date |
2016-11-25T13:20:28Z
2016-11-25T13:20:28Z 2011 |
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Type |
Thesis
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Identifier |
http://krishikosh.egranth.ac.in/handle/1/87505
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Format |
application/pdf
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Publisher |
IARI, DIVISION OF AGRICULTURAL CHEMICALS
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