...
首页> 外文期刊>Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry >SYNTHESIS OF SOME 1-FLUOROARYL-1,3-DIKETONES, BIS(1,3-DIKETONATO)COPPER(II), BIS(1,3-DIKETONATO)DIOXOURANIUM(VI), AND THEIR ELECTROPHILIC SUBSTITUTION REACTIONS
【24h】

SYNTHESIS OF SOME 1-FLUOROARYL-1,3-DIKETONES, BIS(1,3-DIKETONATO)COPPER(II), BIS(1,3-DIKETONATO)DIOXOURANIUM(VI), AND THEIR ELECTROPHILIC SUBSTITUTION REACTIONS

机译:某些1-氟-1,3-二酮,BIS(1,3-二酮酮)铜(II),BIS(1,3-二酮基)二恶古铜(VI)的合成及其亲电取代反应

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Some l-fluoroaryl-l,3-diketones were prepared by treatment of methyl 1-fluoroaryl ketone with ethyl acetate, ethyl fluoroacetate or ethyl pentafluoropropionate in the presence of sodamide which were characterized in the form of their copper chelates. 1-Substituted-aryl-1,3-diketones (la-h) in turn on treatment with uranyl acetate afforded corresponding bis(1,3-diketonato) dioxouranium(VI) (3a-f). Bis(l,3-diketonato)dioxouranium(VI) (3a-f) when subjected to electrophilic bromination or nitration reactions yielded bis(2-bromo-1,3-diketonato)dioxouranium(VI) (4a-e) and bis(2-nitro-1,3-diketonato)dioxouranium(VI) (5a-e), respectively. The bonding mode of the ligands to the uranium ion has also been determined from IR and ~1H NMR spectral studies.
机译:通过在乙酰胺存在下用乙酸乙酯,氟乙酸乙酯或五氟丙酸乙酯处理甲基1-氟芳基酮来制备一些1-氟芳基-1,3-二酮,其特征在于它们的铜螯合物形式。然后用乙酸铀酰处理1-取代的芳基-1,3-二酮(Ia-h),得到相应的双(1,3-二酮基)二氧铀(VI)(3a-f)。进行亲电溴化或硝化反应时,双(1,3-二酮基)二氧铀(VI)(3a-f)产生双(2-溴-1,3-二酮基)二氧铀(VI)(4a-e)和双( 2-硝基-1,3-二酮基)二氧铀(VI)(5a-e)。配体与铀离子的键合模式也已通过IR和〜1H NMR光谱研究确定。

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