Research Article
Environ-Economic Synthesis and Characterization of Some New 1,2,4-Triazole Derivatives as Organic Fluorescent Materials and Potent Fungicidal Agents
Table 8
Antifungal evaluation of the synthesized compounds (5a–p).
| | Zone of inhibition (mm) | Compounds | Concentration (250 ppm) | Concentration (500 ppm) | | A | B | C | D | E | F | A | B | C | D | E | F |
| 5a | 7 | 9 | 8 | 9 | 8 | 8 | 8 | 8 | 10 | 10 | 9 | 10 | 5b | 8 | 7 | 9 | — | — | — | — | 9 | 9 | 10 | — | 11 | 5c | 6 | 9 | — | 8 | 9 | 5 | — | 8 | 9 | — | 12 | 9 | 5d | 4 | — | 10 | — | — | 8 | 9 | — | 9 | — | 11 | — | 5e | — | 8 | 8 | — | 8 | — | 7 | — | 11 | — | — | — | 5f | 7 | 7 | 9 | 9 | — | 6 | — | 8 | 9 | 11 | — | 12 | 5g | 6 | 6 | 10 | 8 | — | — | 9 | 7 | 10 | 9 | 9 | 10 | 5h | 8 | 9 | — | — | 9 | — | 8 | 9 | 11 | — | 11 | 11 | 5i | 8 | 8 | — | — | 8 | 8 | — | 6 | — | — | 10 | — | 5j | 4 | — | 8 | 8 | — | — | 9 | — | 11 | 8 | 9 | — | 5k | 7 | — | 9 | 10 | — | — | 8 | 9 | — | 7 | — | — | 5l | — | 9 | — | — | 9 | 6 | — | 8 | 10 | 10 | 9 | — | 5m | 9 | 10 | 9 | 9 | — | 6 | — | — | 9 | 9 | 9 | 11 | 5n | — | 9 | 8 | 7 | 8 | 8 | — | — | 9 | — | 9 | 9 | 5o | 9 | — | — | — | — | 7 | 8 | — | — | 10 | 7 | 10 | 5p | 8 | 8 | 9 | 7 | 7 | 7 | 7 | 9 | 9 | 11 | 12 | 9 | DMSO | — | — | — | — | — | — | — | — | — | — | — | — | Streptomycin | 11 | 11 | 13 | 12 | 13 | 10 | 11 | — | 12 | 13 | 15 | 14 | Erythromycin | 14 | 13 | 10 | 11 | 12 | 13 | 14 | 10 | — | 14 | 14 | 12 |
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A: Aspergillus niger, B: Penicillium notatum, C: Fusarium oxysporum, D: Alternaria brassicicola, E: Chaetomium orium, F: Lycopodium sp. Bold numbers indicate compounds showing good activity.
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