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丙环唑配合物的合成、缓释性能及生物活性研究
Propiconazole Complexes: Synthesis, Controlled Release Properties and Biological Activities
【摘要】 <正>控制有效成分缓慢释放已成为21世纪农药的主要发展方向之一[1,2],但采用与金属盐反应生成配合物达到缓释目的的研究相对较少[3,4]。农药有效成
【Abstract】 Five propiconazole(L) complexes (ML2Cl2, M=Zn(Ⅱ), Cu(Ⅱ), Co(Ⅱ); ML4Cl2, M=Ni(Ⅱ), Mn(Ⅱ)) were prepared and characterized by elemental analysis and IR. These complexes exhibited favorable controlled release property, it took 40 to 120 hours to release 85% amount of ligand in the water. The toxicity determination to Botrytis cinera, Rhizoctonia cerealis, Gibberella zeae, Fussrium moniliforme and Colletotrichum orbiculare indicated that the fungicidal activities of the complexes were better than that of the ligand except Mn-complex to Rhizoctonia cereali. The EC50 of Zn-propiconazole were 0.045 2~0.144 1 μg·mL-1, Co-and Ni-propiconazole were 0.066 3~0.210 4 μg·mL-1 and 0.183 9~0.340 7 μg·mL-1, respectively, and Mn-propiconazole were only 0.353 6~0.538 0 μg·mL-1. The growth regulation experiment to wheat seeding by dressing treating indicated that inhibiting activities of the complexes to root length and stem height were weaker than that of the ligand.
【Key words】 propiconazole; metal-complex; synthesis; controlled release; biological activity;
- 【文献出处】 无机化学学报 ,Chinese Journal of Inorganic Chemistry , 编辑部邮箱 ,2007年07期
- 【分类号】S482.2
- 【被引频次】23
- 【下载频次】340