Directly Knitted Ruthenium Pincer Complexes with Enhanced Activity as Recyclable Single-Site Catalysts for Hydrogenation of CO2 to Methanol

被引:8
|
作者
Wen, Daheng [1 ]
Chen, Jiangbo [1 ]
Zheng, Qingshu [1 ]
Yang, Siqi [1 ]
Tu, Tao [1 ,2 ,3 ]
机构
[1] Fudan Univ, Dept Chem, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200438, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
[3] Zhengzhou Univ, Green Catalysis Ctr & Coll Chem, Zhengzhou 450001, Peoples R China
来源
CCS CHEMISTRY | 2023年 / 5卷 / 07期
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
direct knitting; hydrogenation of CO2; porous organometallic polymers; ruthenium pincer complexes; single-site catalyst; CARBON-DIOXIDE; CONVERSION; AMINE; FORMYLATION; CAPTURE;
D O I
10.31635/ccschem.022.202202233
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Considering the importance of the valorization of CO2, a number of phosphine-containing ruthenium pincer complexes have been successfully heterogenized using a "direct knitting" strategy without any premodification. The resulting porous organometallic polymers (POMPs) with high specific-surface areas, hierarchical pores, and uniformly dispersed Ru single-sites exhibited outstanding catalytic activity toward the N-formylation of diverse amines with CO2. Besides excellent turnover number (TON, 5 x 10(5)) and turnover frequency (TOF, 5592 h(-1)), the obtained formamides were readily hydrogenated to methanol with the same catalyst. Consequently, an amine-assisted direct hydrogenation system of CO2 to methanol was established by POMPs with higher activity and TON (1.46 x (10)(4)) than their molecular precursors, shedding light on the direct valorization of CO2 and carbon neutral recycling.
引用
收藏
页码:1602 / 1611
页数:10
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