...
首页> 外文期刊>Journal of Sulfur Chemistry >Studies on chromium(III) complexes with active nitrogen, oxygen and sulfur donor ketimines synthesized under microwave conditions
【24h】

Studies on chromium(III) complexes with active nitrogen, oxygen and sulfur donor ketimines synthesized under microwave conditions

机译:微波条件下合成的具有活性氮,氧和硫供体酮的铬(III)配合物的研究

获取原文
获取原文并翻译 | 示例
           

摘要

Heterocyclic ketimines, 1-(2-furanyl)ethanonehydrazincarbothioamide (L1H), 1-(2-furanyl)ethanone- hydrazincarboxamide (L2H), 1-(2-thienyl)ethanone hydrazincarbothioamide (L3H) and 1-(2-thienyl) ethanonehydrazincarboxamide (L4H), were prepared by the condensation of thiosemicarbazide and semicarbazide hydrochloride (in the presence of sodium acetate) in ethanol with the respective ketones by using microwave as well as conventional methods. Chromium(III) complexes have been prepared by mixing CrCl3·6H2O in 1:1 and 1:2 molar ratios with monobasic bidentate ketimines. The authenticity of the ligands and their complexes has been established by elemental analyses, melting point determinations, molecular weight determinations, EPR, infrared and UV spectral and X-ray powder diffraction studies. These studies showed that the ligands coordinated to the metal atom in a monobasic bidentate mode, coordinating through the nitrogen and sulfur/oxygen donor system. Thus, an octahedral environment around the metal atoms has been proposed. The growth-inhibiting potential of the ligands and complexes has been assessed against a variety of fungal and bacterial strains.
机译:杂环酮亚胺,1-(2-呋喃基)乙酮肼甲硫酰胺(L 1 H),1-(2-呋喃基)乙酮-肼甲酰胺(L 2 H),1-(通过缩氨基脲和氨基脲缩合制备2-噻吩基乙酮肼甲碳酰胺(L 3 H)和1-(2-噻吩基)乙酮肼甲酰胺(L 4 H)。 (在乙酸钠存在下)在乙醇中与相应的酮一起通过微波以及常规方法。铬(III)配合物是通过将摩尔比为1:1和1:2的CrCl 3 ·6H 2 O与二元二齿酮亚胺混合而制备的。配体及其配合物的真实性已通过元素分析,熔点测定,分子量测定,EPR,红外和紫外光谱以及X射线粉末衍射研究确定。这些研究表明,配体以二元二齿模式与金属原子配位,通过氮和硫/氧供体系统配位。因此,已经提出了围绕金属原子的八面体环境。已经针对多种真菌和细菌菌株评估了配体和复合物的生长抑制潜力。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号