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3,5-Bis(2-Hydroxyphenyl)-1H-1,2,4-Triazole Derivatives: Synthesis, Crystal Structure and Insecticidal Activity

机译:3,5-双(2-羟基苯基)-1H-1,2,4-三唑衍生物:合成,晶体结构和杀虫活性

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摘要

In an effort to discover new molecules with good insecticidal activities, a series of 3,5-bis (2-hydroxyphenyl)-1H-1,2,4-triazole derivatives were synthesized. The X-ray crystallographic and Hirshfeld surface calculation study of compound 4c reveal the structural characteristics and strong intermolecular interactions and also evaluated for it's insecticidal activity. The bioassays data demonstrate that all the target compounds possess remarkable activities against broad bean aphid with the mortal- ities ranging from 98.12% to 100% at the concentration of 100 mg/L. In particular, methyl 4-[3,5-bis(2-hydroxyphenyl)-1H- 1,2,4-triazol-1-yl] benzoate (85.53%) shows higher activity than dinotefuran (85.25%) at the concentration of 10 mg/L whereas other compounds display low activity at the same concen- tration. The docking model of compound 4a shows possible mechanism of insecticidal action of target compounds.
机译:为了发现具有良好杀虫活性的新分子,合成了一系列3,5-双(2-羟基苯基)-1H-1,2,4-三唑衍生物。 化合物4C的X射线晶体学和Hirshfeld表面计算研究揭示了结构特征和强分子间相互作用,还评估了其杀虫活性。 生物测定数据表明,所有目标化合物都具有针对宽豆蚜虫的显着活性,其凡人的浓度范围从98.12%到100%。 特别是,甲基4- [3,5-双基(2-羟基苯基)-1H- 1,2,4-三唑-1-基]苯甲酸酯(85.53%)在浓度下显示出比Dinotefuran(85.25%)更高的活性。 10 mg/l,而其他化合物在相同的浓度下表现出较低的活性。 化合物4a的对接模型显示了靶化合物杀虫作用的可能机制。

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