Tandem hydroformylation/hydrogenation of olefins to alcohols using atomically dispersed bifunctional catalysts

被引:1
|
作者
Zhang, Ying [1 ]
Liu, Liyang [1 ]
Wang, Ziyue [1 ]
Zhang, Xingcong [1 ]
He, Xiaohui [1 ,3 ]
Ji, Hongbing [1 ,2 ]
机构
[1] Sun Yat sen Univ, Fine Chem Ind Res Inst, Sch Chem, Key Lab Bioinorg & Synthet Chem Minist Educ ,IGCM, Guangzhou 510275, Peoples R China
[2] Zhejiang Univ Technol, Inst Green Petr Proc & Light Hydrocarbon Convers, Coll Chem Engn, State Key Lab Breeding Base Green Chem Synth Techn, Hangzhou 310014, Peoples R China
[3] Guangdong Technol Res Ctr Synth & Separat Thermose, Guangzhou 510275, Peoples R China
基金
中国国家自然科学基金;
关键词
tandem; hydroformylation/hydrogenation; alcohols; bifunctional; single atom catalysts; REDUCTIVE-HYDROFORMYLATION; HYDROGENATION;
D O I
10.1007/s11426-024-2135-y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Tandem hydroformylation/hydrogenation of olefins to alcohols is an appealing and challenging route that has received continuous interest. Herein, we report a bifunctional atomically dispersed Rh and Co catalyst (RhCo/Al2O3-10) prepared by a simple ball milling method that displays superior synergistic catalytic performance (>95% olefins conversion and >80% alcohols selectivity) and broad substrate scope for tandem hydroformylation/hydrogenation reaction, outperforming Rh/Al2O3, Co/Al2O3, and their physically mixed counterparts. In situ CO-DRIFTS, XPS, and kinetic experiments demonstrate that the electron interaction between Rh and Co atoms effectively lowers the apparent activation energy, thus promoting the tandem hydroformylation/hydrogenation reaction. This work not only presents a novel tandem hydroformylation/hydrogenation reaction system for converting olefins to alcohol but also throws light on the rational design of versatile bifunctional catalysts for on-demand synergistic catalysis.
引用
收藏
页码:3706 / 3711
页数:6
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