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Synergistic actions between tebuconazole ligand and Cu(II) cation: reasons for the enhanced antifungal activity of four Cu(II) complexes based on the fungicide tebuconazole

机译:戊唑醇配体与铜(II)阳离子之间的协同作用:增强基于戊唑醇的四种铜(II)配合物抗真菌活性的原因

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摘要

Four Cu(II) complexes, namely, [CuL2(SO4)(DMF)](n) 1, [CuL2(CH3COO)(2)](2), [CuL4Cl2]center dot 2DMF center dot 3H(2)O 3 and [CuL4(ClO4)(2)] 4, (L = ((RS)-1-(4-chloro-phenyl)-4,4-dimethyl-3-(1,2,4-triazole-1-ylmethyl)pentan-3-ol), tebuconazole) have been synthesized and their structures were identified by elemental analysis (EA), infrared (IR) spectroscopy and single crystal X-ray diffraction (XRD). Moreover, the four obtained complexes were screened for antifungal activities against four selected fungi using the mycelial growth rate method. Structural analysis indicates that the different coordination modes of the ligands and counter anions contribute to a one-dimensional polymer chain structure in complex 1 and zero-dimensional mononuclear structures in complexes 2-4. The results of the antifungal activities show that all the complexes synthesized show better antifungal activities than the ligand L. In addition, the mechanism of the increased antifungal activities of the title complexes in comparison with the ligand was discussed preliminarily and the synergistic interaction between Cu2+ and tebuconazole was also investigated by the Wadley approach.
机译:四种Cu(II)配合物,即[CuL2(SO4)(DMF)] [n] 1,[CuL2(CH3COO)(2)](2),[CuL4Cl2]中心点2DMF中心点3H(2)O 3和[CuL4(ClO4)(2)] 4,(L =((RS)-1-(4-氯-苯基)-4,4-二甲基-3-(1,2,4-三唑-1-基甲基戊三醇),戊唑醇)已经合成,并通过元素分析(EA),红外(IR)光谱和单晶X射线衍射(XRD)鉴定了它们的结构。此外,使用菌丝生长速率法筛选了四种获得的复合物对四种选定真菌的抗真菌活性。结构分析表明,配体和抗衡阴离子的不同配位方式有助于配合物1中的一维聚合物链结构和配合物2-4中的零维单核结构。抗真菌活性的结果表明,所有合成的配合物均具有比配体L更好的抗真菌活性。此外,与配体相比,初步探讨了标题配合物抗真菌活性增强的机理,并探讨了Cu2 +与Cu2 +之间的协同作用。戊唑醇也通过Wadley方法进行了研究。

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