...
首页> 外文期刊>Journal of the Chemical Society, Perkin Transactions 1 >Multiple substitutions on (η6-arene)tricarbonylchromium(0) complexes
【24h】

Multiple substitutions on (η6-arene)tricarbonylchromium(0) complexes

机译:(η6-芳烃)三羰基铬(0)络合物的多次取代

获取原文
获取原文并翻译 | 示例

摘要

The treatment of representative (η6-arene)tricarbonylchromium(0) complexes 1a–c and 4 with 3 equivalents ofnLiTMP followed by an electrophilic quench with Me3SiCl provided a series of trisilylated complexes 2a–c and 5a. Thenuse of Me3SnCl and Ph2PCl as electrophile also yielded unusual trisubstituted complexes 13a and 13b. The X-rayncrystallographic structure of complex 13b is reported. Deuteration studies using deuteroacetic acid as the electrophilenled to the observation of a trideuterated species presumably derived from a trianionic species formed during thenreaction. Efficient disubstitution was observed when complexes 7, 9 and 11 were treated with 3 equivalents of LDAnfollowed by an electrophilic quench with Me3SiCl
机译:用3当量的nLiTMP处理代表性的(η6-芳烃)三羰基铬(0)配合物1a–c和4,然后用Me3SiCl进行亲电淬灭,提供了一系列三甲硅烷基化的配合物2a–c和5a。然后使用Me 3 SnCl和Ph 2 PCl作为亲电试剂也产生了不寻常的三取代的配合物13a和13b。报道了配合物13b的X射线晶体学结构。使用氘代乙酸作为亲电子试剂进行氘化研究,以观察到可能是由在反应过程中形成的三阴离子物质衍生的三氘代物质。当配合物7、9和11用3当量的LD处理后,观察到有效的去污作用,随后用Me3SiCl进行了亲电淬灭

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