...
首页> 外文期刊>Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry >Electrophilic Addition of Phenylisocyanate at #x3B3;-CH of Thio-#x3B2;-diketonates of Some Transition Metals
【24h】

Electrophilic Addition of Phenylisocyanate at #x3B3;-CH of Thio-#x3B2;-diketonates of Some Transition Metals

机译:Electrophilic Addition of Phenylisocyanate at #x3B3;-CH of Thio-#x3B2;-diketonates of Some Transition Metals

获取原文
   

获取外文期刊封面封底 >>

       

摘要

The quasi-aromatic property of metal chelates of thio-#x3B2;-diketones has been studied by reacting them with phenylisocyanate, where addition takes place at the #x3B3;-CH in a stepwise manner. Mono-thiodiketonates of Ni(II), Pd(II), cu(II) and Co(III) and the dithio-acetylacetonate of Ni(II) react with phenylisocyanate to produce mono-, di- and triphenylamido with cobalt (III) only substituted derivatives. In the case of tris (ethylthioacetoacetato) cobalt (III), it is found that the reaction with phenylisocyanate gives two isomers, a chocolate coloured isomer in which the phenylamido carbonyl is not coordinated while the green coloured isomer has bonding through phenylemido carbonyl oxygen. The reactions of the thiodiketonates have been compared with those of #x3B2;-diketonates and #x3B2;-ketoiminates. The reaction products have been characterised by elemental analyses, magnetic moments, and electronic, IR and1H NMR spectral studies.

著录项

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