脱羧
光催化
光化学
激进的
化学
催化作用
碳纤维
羧酸
氮化碳
材料科学
有机化学
无机化学
复合数
复合材料
作者
Jiale Shi,Yuan Tao,Meifang Zheng,Xinchen Wang
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2021-02-23
卷期号:11 (5): 3040-3047
被引量:89
标识
DOI:10.1021/acscatal.0c05211
摘要
A suitable protocol for the photocatalytic decarboxylation of carboxylic acids was developed with metal-free ceramic boron carbon nitrides (BCN). With visible light irradiation, BCN oxidize carboxylic acids to give carbon-centered radicals, which were trapped by hydrogen atom donors or employed in the construction of the carbon–carbon bond. In this system, both (hetero)aromatic and aliphatic acids proceed the decarboxylation smoothly, and C–H, C–D, and C–C bonds are formed in moderate to high yields (35 examples, yield up to 93%). Control experiments support a radical process, and isotopic experiments show that methanol is employed as the hydrogen atom donor. Recycle tests and gram-scale reaction elucidate the practicability of the heterogeneous ceramic BCN photoredox system. It provides an alternative to homogeneous catalysts in the valuable carbon radical intermediates formation. Moreover, the metal-free system is also applicable to late-stage functionalization of anti-inflammatory drugs, such as naproxen and ibuprofen, which enrich the chemical toolbox.
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