Efficient light-driven reductive amination of furfural to furfurylamine over ruthenium-cluster catalyst
Efficient light-driven reductive amination of furfural to furfurylamine over ruthenium-cluster catalyst作者机构:State Key Laboratory of Chemical Resource EngineeringBeijing University of Chemical TechnologyBeijing 100029China Department of ChemistryTsinghuaUniversityBeijing 10084China Institute of High Energy PhysicsThe Chinese Academy of SciencesBeijing 100049China
出 版 物:《Journal of Energy Chemistry》 (能源化学(英文版))
年 卷 期:2023年第76卷第1期
页 面:239-248,I0007页
核心收录:
学科分类:081705[工学-工业催化] 08[工学] 0817[工学-化学工程与技术] 080502[工学-材料学] 0805[工学-材料科学与工程(可授工学、理学学位)]
基 金:financially supported by the National Natural Science Foundation of China(202102007,21978147 and 21935001) the Fundamental Research Funds for the Central Universities(buctrc202112)
主 题:Furfural Reductive amination Ru nanoclusters Hydrogen transfer Photocatalysis
摘 要:Selective reductive amination of carbonyl compounds with high activity is very essential for the chemical and pharmaceutical industry,but scarcely successful paradigm was reported via efficient photocatalytic ***,the ultrasmall Ru nanoclusters(~0.9 nm)were successfully fabricated over P25 support with positive charged Ru^(δ+)species at the interface.A new route was developed to achieve the furfural(FAL)to furfurylamine(FAM)by coupling the light-driven reductive amination and hydrogen transfer of ethanol over this type ***,the photocatalytic activity and selectivity are strongly dependent on the particle size and electronic structure of *** Ru^(δ+)species at the interface promote the formation of active imine intermediates;moreover,the Ru nanoclusters facilitate the separation efficiency of electrons and holes as well as accelerate the further hydrogenation of imine intermediates to product primary *** contrast Ru particles in larger nanometer size facilitate the formation of the furfuryl alcohol and excessive hydrogenation *** addition,the coupling byproducts can be effectively inhibited via the construction of *** study offers a new path to produce the primary amines from biomass-derived carbonyl compounds over hybrid semiconductor/metal-clusters photocatalyst via light-driven tandem catalytic process.