催化作用
烷基
苯乙酮
键裂
芳基
选择性
碳纤维
化学
材料科学
多相催化
表面改性
有机化学
复合数
物理化学
复合材料
作者
Yushan Wu,Yao Luo,Siyi Huang,Jida Wang,Junchen Xu,Xiang‐Kui Gu,Mingyue Ding
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2025-01-16
卷期号:15 (3): 1704-1714
标识
DOI:10.1021/acscatal.4c06769
摘要
Efficient and selective cleavage and functionalization of C–C bonds is of critical significance in fine chemistry and lignocellulosic biomass valorization, yet it is still challenging due to their inert nature. In the present work, we report an atomically dispersed Cu catalyst encapsulated in N-doped porous carbon (Cu@NC-900) through a facile method using metal–organic frameworks (MOFs) as precursors, where Cu atoms were chelated and stabilized by N species. The resulting catalyst exhibited good performance for oxidative cleavage of C–C bonds toward esters, giving a 98.6% yield of methyl benzoate with complete conversion of acetophenone under base-free conditions. Further, the Cu@NC-900 catalyst was efficient for the conversion of a wide range of ketones, including (hetero)aryl methyl ketones or challenging alkyl ketones, to their corresponding esters. Experiments demonstrated that the highly dispersed Cu sites and incorporation of N species, as well as the rich pore structures, contributed to the high activity, selectivity, and stability. Theoretical calculations further attributed the high activity to the oxidation state formed by the electron loss of the isolated Cu atoms.
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