...
首页> 外文期刊>Asian Journal of Organic Chemistry >Seven-Coordinate Mo-II-Diiodo Complexes with Benzothiazole-N-Heterocyclic-Carbene Ligands and Their Mo-0 Precursors: Synthesis, Structures, and Catalytic Application in the Epoxidation of cis-Cyclooctene
【24h】

Seven-Coordinate Mo-II-Diiodo Complexes with Benzothiazole-N-Heterocyclic-Carbene Ligands and Their Mo-0 Precursors: Synthesis, Structures, and Catalytic Application in the Epoxidation of cis-Cyclooctene

机译:七坐标MO-II-二碘聚合物与苯并噻唑-N-杂环 - 卡宾配体及其MO-0前体:合成,结构和催化应用在CIS-Cyclocene的环氧化中

获取原文
获取原文并翻译 | 示例
           

摘要

The oxidative addition of I-2 to molybdenum(0) complexes [Mo(CO)(4)(L-NC)] (1-3; L-NC1 = 1-(benzothiazolin-2-yl)-3-allyl-2-ylidene; L-NC2 = 1-(benzothiazolin-2-yl)-3-benzylimidazol-2-ylidene; L-NC3 = 1-(benzothiazolin-2-yl)-3-methylimidazol-2-ylidene) afforded the first isolable and crystallographically elucidated seven-coordinate Mo-II-diiodo complexes, [Mo(-CO)(3)I-2(L-NC)] (4-6), with N-heterocyclic carbene (NHC) ligands(.) The application of complexes 1-6 as precatalysts for the epoxidation of cis-cyclooctene with tert-butyl hydroperoxide (TBHP) as an oxidant has also been studied. Complexes 1-3 performed better than previously reported Mo-0-carbonyl-NHC complexes, thereby producing the epoxide in 80-90% yield after 24h. Complexes 4-6 were superior to complexes 1-3. Complex 5 was the most-active Mo-II-NHC complex, thereby achieving the epoxide in quantitative yield after 6h.
机译:I-2至钼(0)复合物[Mo(CO)(4)(4)(L-NC)](1-3; L-NC1 = 1-(苯并噻唑啉-2-基)-3-烯丙基 - 2- ylidene; L-NC2 = 1-(苯并噻唑啉-2-基)-3-苄基咪唑-2- ylidene; L-NC3 = 1-(苯并噻唑啉-2-基)-3-甲基咪唑-2- ylidene)提供了 首先分离和晶形释放的七坐标Mo-II-二碘聚合物,[Mo(-Co)(3)I-2(L-NC)](4-6),用正杂环癸烯(NHC)配体(。 [还研究了作为氧化剂的叔丁基氢过氧化氢(TBHP)的CIS-COPOXIDENOXIDOXINATION的络合物1-6的施用。 复合物1-3比以前报道的MO-0-羰基-NHC复合物更好,从而在24小时后产生80-90%产率的环氧化物。 复合物4-6优于复合物1-3。 复合物5是最活跃的MO-II-NHC复合物,从而在6小时后以定量产率达到环氧化物。

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