Hydroformylation of Olefins with CO2/H2 and Hydrosilane by Copper/Cobalt Tandem Catalysis

被引:8
作者
Wu, An-Guo [1 ,2 ]
Ding, Jie [1 ,2 ]
Zhao, Lan [1 ,2 ]
Li, Hong-Ru [1 ,3 ]
He, Liang-Nian [1 ,2 ]
机构
[1] Nankai Univ, Coll Chem, State Key Lab, Tianjin 300071, Peoples R China
[2] Nankai Univ, Inst Elementoorgan Chem, Coll Chem, Tianjin 300071, Peoples R China
[3] Nankai Univ, Coll Pharm, Tianjin 300350, Peoples R China
基金
中国国家自然科学基金;
关键词
carbon dioxide; hydroformylation; earth abundant metal; ligand design; tandem catalysis; CARBON-MONOXIDE; CO2; ALKENES; HYDROGENATION; REDUCTION; PHOSPHINE; COMPLEXES; DIOXIDE;
D O I
10.1002/cssc.202400608
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A Cu/Co tandem catalysis protocol was developed to conduct the hydroformylation of olefins using CO2/H-2 and PMHS (polymethylhydrosiloxane) as a readily available and environmentally friendly hydride source. This methodology was performed via a two-step approach consisting of the copper-catalyzed reduction of CO2 by hydrosilane and subsequent cobalt-promoted hydroformylation with H-2 and the in situ formed CO. The optimized triphos oxide ligand, which presumably facilitates the migratory insertion of CO gives moderate to excellent yields for both terminal and internal alkenes. This earth-abundant metal catalysis provides a reliable and efficient way to afford useful aldehydes in industry using silicon by-product PMHS as hydrogen source and renewable CO2 as carbonyl source.
引用
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页数:7
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