首页> 外文期刊>Chemistry: A European journal >Mechanism and Applications of the Photoredox Catalytic Coupling of Benzyl Bromides
【24h】

Mechanism and Applications of the Photoredox Catalytic Coupling of Benzyl Bromides

机译:苄基溴的光氧化还原催化偶联的机理与应用

获取原文
获取原文并翻译 | 示例
           

摘要

The photoredox catalytic coupling of halomethyl arenes to bibenzyl derivatives has been demonstrated. The catalytic protocol employed the Hantzsch ester, potassium phosphate, and a photoactive cyclometalated Ir-III complex catalyst. A photochemical quantum yield as high as 20% was obtained. The catalytic mechanism was investigated in detail by performing photophysical and electrochemical measurements, as well as by quantum chemical calculations. The results suggest that two-electron mediation might be responsible for the improved photon economy. The reaction protocol was compatible with halomethyl arenes that contain a variety of functional groups. Finally, the synthetic utility of our protocol was demonstrated by the preparation of a natural dihydrostilbenoid, brittonin A.
机译:已经证明卤代甲基芳烃与联苄衍生物的光氧化还原催化偶联。催化方案使用Hantzsch酯,磷酸钾和光敏环金属化Ir-III络合物催化剂。获得了高达20%的光化学量子产率。通过进行光物理和电化学测量以及量子化学计算,详细研究了催化机理。结果表明,双电子介导可能是改善光子经济的原因。该反应方案与含有多种官能团的卤代甲基芳烃兼容。最后,我们的方案的合成实用性通过制备天然的二氢芪类化合物布列通A来证明。

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