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Paired Oxidative and Reductive Catalysis: Breaking the Potential Barrier of Electrochemical C(sp3)−H Alkenylation**
Angewandte Chemie International Edition ( IF 16.1 ) Pub Date : 2023-04-01 , DOI: 10.1002/anie.202301026 Long Zou 1 , Xiaofan Wang 1 , Siqi Xiang 1 , Weipeng Zheng 1 , Qingquan Lu 1
Angewandte Chemie International Edition ( IF 16.1 ) Pub Date : 2023-04-01 , DOI: 10.1002/anie.202301026 Long Zou 1 , Xiaofan Wang 1 , Siqi Xiang 1 , Weipeng Zheng 1 , Qingquan Lu 1
Affiliation
A paired electrocatalysis strategy for alkane functionalization is reported for the first time, in which earth-abundant iron and nickel are employed as the anodic and cathodic catalysts, respectively. Importantly, C(sp3)−H alkenylation of alkanes with ultra-low oxidation potential (≈0.25 V vs. Ag/AgCl) is achieved using this protocol, providing a modular method for versatile mono- or multi-substituted olefins under mild conditions.
中文翻译:
配对氧化还原催化:打破电化学 C(sp3)−H 烯基化的势垒**
首次报道了一种用于烷烃功能化的配对电催化策略,其中地球丰富的铁和镍分别用作阳极和阴极催化剂。重要的是,使用该协议实现了具有超低氧化电位(≈0.25 V vs. Ag/AgCl)的烷烃的 C(sp 3 )−H 烯基化,为温和条件下的多功能单取代或多取代烯烃提供了模块化方法.
更新日期:2023-04-01
中文翻译:
配对氧化还原催化:打破电化学 C(sp3)−H 烯基化的势垒**
首次报道了一种用于烷烃功能化的配对电催化策略,其中地球丰富的铁和镍分别用作阳极和阴极催化剂。重要的是,使用该协议实现了具有超低氧化电位(≈0.25 V vs. Ag/AgCl)的烷烃的 C(sp 3 )−H 烯基化,为温和条件下的多功能单取代或多取代烯烃提供了模块化方法.