首页> 外文期刊>Chemistry: A European journal >Solvent-Dependent Interconversions between Rh~I,Rh~(II),and Rh~(III)Complexes of an Aryl-Monophosphine Ligand
【24h】

Solvent-Dependent Interconversions between Rh~I,Rh~(II),and Rh~(III)Complexes of an Aryl-Monophosphine Ligand

机译:芳基-单膦配体的Rh〜I,Rh〜(II)和Rh〜(III)配合物之间的溶剂依赖性转换

获取原文
获取原文并翻译 | 示例
           

摘要

Reaction of the aryl-mono-phosphine ligand alpha~2-(diisopropylphos-phino)isodurene(1)with the Rh~I precursor [Rh(coe)2(acetone)2]BF4(coe = cyclooctene)in different solvents yielded complexes of all three common oxidation states of rhodium,depending on the solvent used.When the reaction was carried out in methanol a cyclome-talated,solvent-stabilized Rh~(III)alkyl- hydride complex(2)was obtained.However,when the reaction was carried out in acetone or dichloromethane a dinuclear eta~6-arene Rh~(II)complex(5)was obtained in the absence of added redox reagents.Moreover,when aceto-nitrile was added to a solution of either the Rh~(II)or Rh~(III)complexes,a new solvent-stabilized,noncyclometalated Rh~I complex(6)was obtained.In this report we describe the different complexes,which were fully characterized,and probe the processes behind the remarkable solvent effect observed.
机译:芳基-单膦配体α〜2-(二异丙基膦基)异二烯(1)与Rh〜I前体[Rh(coe)2(丙酮)2] BF4(coe =环辛烯)的反应生成复合物取决于所使用的溶剂,在所有三种常见的铑氧化态中。当在甲醇中进行反应时,会得到环金属化的,溶剂稳定的Rh〜(III)烷基氢化物(2)。在丙酮或二氯甲烷中进行反应,在不添加氧化还原试剂的情况下,获得了双核的η〜6-芳烃Rh〜(II)络合物(5)。此外,在向Rh〜的溶液中加入乙腈时(II)或Rh〜(III)配合物,获得了一种新型的溶剂稳定的非环金属化Rh〜I配合物(6)。在本报告中,我们描述了各种配合物,并对其进行了全面表征,并探讨了该显着溶剂背后的过程。观察到的效果。

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