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
作者单位
杨春龙 南京农业大学理学院化学系南京 210095 
罗金香 南京农业大学理学院化学系南京 210095 
谢学群 南京农业大学理学院化学系南京 210095 
李前进 南京农业大学理学院化学系南京 210095 
顾颖迪 南京农业大学理学院化学系南京 210095 
田艳丽 南京农业大学理学院化学系南京 210095 
朱兆勇 南京农业大学理学院化学系南京 210095 
摘要: 
关键词: 丙环唑  金属配合物  合成  缓释  生物活性
基金项目: 
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.
Keywords: propiconazole  metal-complex  synthesis  controlled release  biological activity
 
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杨春龙,罗金香,谢学群,李前进,顾颖迪,田艳丽,朱兆勇.丙环唑配合物的合成、缓释性能及生物活性研究[J].无机化学学报,2007,23(7):1259-1263.
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