{"title":"Atomically Dispersed Cu Atoms Anchored on N-Doped Porous Carbon as an Efficient Catalyst for C–C Bond Cleavage of Ketones toward Esters","authors":"Yushan Wu, Yao Luo, Siyi Huang, Jida Wang, Junchen Xu, Xiang-Kui Gu, Mingyue Ding","doi":"10.1021/acscatal.4c06769","DOIUrl":null,"url":null,"abstract":"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.","PeriodicalId":9,"journal":{"name":"ACS Catalysis ","volume":"27 1","pages":""},"PeriodicalIF":11.3000,"publicationDate":"2025-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Catalysis ","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acscatal.4c06769","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
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.
期刊介绍:
ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels.
The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.