Qu Yang, Tateno Hiroyuki, Matsumura Yoshimasa, Kashiwagi Tsuneo, Atobe Mahito
Graduate School of Environment and Information Sciences, Yokohama National University, 79-7, Tokiwadai, Hodogaya-ku, Yokohama 240851, Japan.
Molecules. 2017 Mar 7;22(3):413. doi: 10.3390/molecules22030413.
We have successfully developed a novel cathodic cross-coupling reaction of aryl halides with arenes. Utilization of the cathodic single electron transfer (SET) mechanism for activation of aryl halides enables the cross-coupling reaction to proceed without the need for any transition metal catalysts or single electron donors in a mild condition. The SET from a cathode to an aryl halide initiates a radical chain by giving an anion radical of the aryl halide. The following propagation cycle also consists entirely of anion radical intermediates.
我们成功开发了一种新型的芳基卤化物与芳烃的阴极交叉偶联反应。利用阴极单电子转移(SET)机制活化芳基卤化物,使得交叉偶联反应能够在温和条件下无需任何过渡金属催化剂或单电子供体即可进行。从阴极到芳基卤化物的单电子转移通过产生芳基卤化物的阴离子自由基引发自由基链反应。接下来的增长循环也完全由阴离子自由基中间体组成。