化学
背景(考古学)
烯烃
电化学
组合化学
羧化
二氧化碳电化学还原
氧化还原
二氧化碳
还原(数学)
化学还原
有机化学
反应机理
选择性
固碳
反应条件
光化学
碳纤维
过程(计算)
化学反应
电催化剂
作者
Xinya Lv,Chunlei Liu,Li Liu,Y. Huang,Yuan Xu,Zhaoliang Yang,Jianye Zhang
标识
DOI:10.1021/acs.joc.5c02850
摘要
Carbon dioxide (CO2), as an ideal single-carbon source in chemical synthesis, has garnered extensive attention for its direct utilization. The direct conversion of CO2 via electrochemistry, an environmentally benign strategy, offers a crucial direction and immense potential for resource transformation in the context of carbon neutrality goals. However, due to the extremely low reduction potential of CO2 itself, the electrochemical carboxylation process often inevitably leads to the formation of multiple products, resulting in poor reaction selectivity. To tackle this challenge, a photoelectrochemical strategy is reported for the efficient reduction of CO2 and the anti-Markovnikov selective carboxylation of activated and unactivated alkenes. The reaction is simple to perform, requiring no additional chemical oxidants throughout the process. Experimental verification confirms that it exhibits excellent applicability to a wide range of alkene substrates, thereby providing a new pathway for highly selective and green carboxylation synthesis.
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