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B-H and O-H bonds activation via a single electron transfer of frustrated radical pairs

机译:通过单个电子传递的令人沮丧的自由基对,B-H和O-H键激活

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摘要

The rare examples of B-H bond activation in a frustrated radical pair regime have been observed by treatment of TEMPO radicals with Piers' borane HB(C6F5)(2) or bis-borane, respectively. The resulting concomitant formation of zwitterionic products and geminal N/B frustrated Lewis pairs implied a one electron process. In addition, the reaction of a TEMPO/B(C6F5)(3) pair with H2O center dot B(C6F5)(3) was assumed to involve one-electron reduction of water. Our results provide insights into chemical bond (e.g. B-H and O-H) activation via a single electron transfer.
机译:通过分别用皮尔斯硼烷HB(C6F5)(2)或双硼烷处理TEMPO自由基,观察到了在受挫折的自由基对区域中B-H键激活的罕见例子。由此产生的两性离子产物和双子N/B受挫刘易斯对的同时形成意味着一个单电子过程。此外,TEMPO/B(C6F5)(3)对与H2O中心点B(C6F5)(3)的反应假定涉及水的单电子还原。我们的结果提供了通过单电子转移激活化学键(例如B-H和O-H)的见解。

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