High-Entropy Lanthanide-Organic Framework as an Efficient Heterogeneous Catalyst for Cycloaddition of CO2 with Epoxides and Knoevenagel Condensation

被引:4
|
作者
Jin, Siyang [1 ]
Fu, Yu [1 ]
Jie, Kecheng [2 ]
Dai, Huan [1 ]
Luo, Yun Jie [1 ]
Ye, Liang [1 ]
Zhou, Chaohui [1 ]
Xu, Wei [1 ]
机构
[1] Ningbo Univ, Resource Recycling, Sch Mat Sci & Chem Engn, Ningbo Shuangneng Environm Technol Co Ltd, Ningbo 315211, Peoples R China
[2] Nanjing Univ, Key Lab Mesoscop Chem MOE, Jiangsu Key Lab Adv Organ Mat, State Key Lab Coordinat Chem,Sch Chem & Chem Engn, Nanjing 210023, Peoples R China
基金
中国国家自然科学基金;
关键词
High-Entropy; Lanthanide-Organic Framework; Dual-Functional Catalyst; CO2; Fixation; Knoevenagel Condensation; CYCLIC CARBONATES; CHEMICAL FIXATION; LEWIS-ACID; METAL; DIOXIDE; CHALLENGES; SEPARATION; CONVERSION; PROGRESS; CAPTURE;
D O I
10.1002/chem.202400756
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Multimetallic synergistic effects have the potential to improve CO2 cycloesterification and Knoevenagel reaction processes, outperforming monometallic MOFs. The results demonstrate superior performance in these processes. To investigate this, we created and characterized a selection of single-component Ln(III)-MOFs (Ln=Eu, Tb, Gd, Dy, Ho) and high-entropy lanthanide-organic framework (HE-LnMOF) using solvent-thermal conditions. The experiments revealed that HE-LnMOF exhibited heightened catalytic efficiency in CO2 cycloesterification and Knoevenagel reactions compared to single-component Ln(III) MOFs. Moreover, the HE-LnMOF displayed significant stability, maintaining their structural integrity after five cycles while sustaining elevated conversion and selectivity rates. The feasible mechanisms of catalytic reactions were also discussed. HE-LnMOF possess multiple unsaturated metal centers, acting as Lewis acid sites, with oxygen atoms connecting the metal, and hydroxyl groups on the ligand serving as base sites. This study introduces a novel method for synthesizing HE-LnMOF and presents a fresh application of HE-LnMOF for converting CO2.
引用
收藏
页数:12
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