...
首页> 外文期刊>Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry >Preparation and investigation of Ce(III), Th(IV) and U(VI) chelates with some Schiff bases derived from 5,7-dihydroxy-6-formyl-2-methylbenzopyran-4-one
【24h】

Preparation and investigation of Ce(III), Th(IV) and U(VI) chelates with some Schiff bases derived from 5,7-dihydroxy-6-formyl-2-methylbenzopyran-4-one

机译:具有5,7-二羟基-6-甲酰基-2-甲基苯并吡喃-4-酮的一些席夫碱的Ce(III),Th(IV)和U(VI)螯合物的制备和研究

获取原文
获取原文并翻译 | 示例

摘要

Schiff bases were prepared by condensation ofequimolar amounts of 5,7-dihydroxy-6-formyl-2-methylbenzopyran-4-one and aniline, anthranilic acid, 2-aminophenol, 5-chloro-2-aminophenol or 4-amino-3-hydroxybenzenesulphonic acid. The molecular structure of theprepared Schiff bases was confirmed by mass and UV spectra. Thechelates of Ce (III), Th (IV), and U (VI) with the above Schiffbases were prepared. All the prepared compounds were bubjectedto elemental analyses for C, H, N, Cl, S and metal (for thechelates), IR and 1H NMR spectroscopy. The studies show that Ce(III) and Th (IV) give 1:1, 1:2 (M: L) metal chelates, while U (VI)gives only 1:1 and 1:2 (M:L) chelates. This may be attributed tothe difficulty of coordinating two bulky uranyl ions to the samemolecule because of their steric effect. The studies revealed thatthe Ce (III) and Th (IV) chelates exhibit octahedral structure withthe coordination number 6 while U (VI) chelates exhibitdodecahedral structure with the coordination number 8.Thermogravimetric analysis data were obtained for some of theprepared chelates.
机译:通过等摩尔量的5,7-二羟基-6-甲酰基-2-甲基苯并吡喃-4-酮与苯胺,邻氨基苯甲酸,2-氨基苯酚,5-氯-2-氨基苯酚或4-氨基-3-苯酚缩合制备席夫碱羟基苯磺酸。制备的席夫碱的分子结构由质谱和紫外光谱证实。制备具有上述席夫碱的Ce(III),Th(IV)和U(VI)的螯合物。所有制备的化合物均经过碳,氢,氮,氯,硫和金属(用于螯合物)的元素分析,IR和1H NMR光谱分析。研究表明Ce(III)和Th(IV)给出1:1,1:2(M:L)的金属螯合物,而U(VI)仅给出1:1和1:2(M:L)的螯合物。这可能归因于由于其空间效应而难以将两个大体积的铀酰离子配位至同一分子。研究表明,铈(III)和Th(IV)螯合物表现出配位数为8的八面体结构,而U(VI)螯合物表现出配位数为8的十二面体结构。获得了一些制备的螯合物的热重分析数据。

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