Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/59341
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dc.contributor.authorFeng, Xiaojun-
dc.contributor.authorWang, Fangkuo-
dc.contributor.authorLiu, Weiguo-
dc.contributor.authorDong, Huaze-
dc.date.accessioned2022-03-23T10:17:24Z-
dc.date.available2022-03-23T10:17:24Z-
dc.date.issued2022-03-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/59341-
dc.description298-304en_US
dc.description.abstractThis study synthesizes two new Schiff bases, (E)-1-(4-1H-imidazol-1-yl)phenyl)-N-(o-tolyl)methanimine and (E)-1-(4-(1Himidazol- 1-yl)phenyl)-N-(m-tolyl)methanimine through condensation reaction between 4-(imidazol-1-yl)benzaldehyde and 2-toluidine/o-toluidine, respectively. FT-IR, X-ray diffraction and 1H NMR spectroscopy have been carried out to characterize the structure of the products. Through antibacterial/ antifungal activity tests performed using 8 kinds of bacteria/fungus, it is found that the both of the two Schiff bases can suppress the growth of Staphylococcus, Bacillus subtilis and Salmonella, showing good potential as antibacterial drug.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR, Indiaen_US
dc.sourceIJC Vol.61(03) [March 2022]en_US
dc.subjectSchiff baseen_US
dc.subjectantibacterial activityen_US
dc.subjectcrystal structureen_US
dc.titleGreen synthesis and antibacterial/fungal studies of two new Schiff base derived from 4-(imidazol-1-yl)benzaldehydeen_US
dc.typeArticleen_US
Appears in Collections:IJC Vol.61(03) [March 2022]

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