Imidazolium carboxylates boost Ru-catalyzed hydroaminomethylation of olefins with CO2

被引:3
|
作者
Qian, Chun [1 ]
Zheng, Qingshu [2 ]
Ji, Jiale [1 ]
Liang, Guanfeng [1 ]
Tu, Bo [1 ]
Tu, Tao [1 ,3 ]
机构
[1] Fudan Univ, Dept Chem, Shanghai Key Lab Mol Catalysis & Innovat Mat, 2005 Songhu Rd, Shanghai 200438, Peoples R China
[2] Shanghai Jiao Tong Univ, Zhangjiang Inst Adv Study, Frontiers Sci Ctr Transformat Mol, Shanghai 200240, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
来源
CHEM CATALYSIS | 2023年 / 3卷 / 11期
基金
中国国家自然科学基金;
关键词
N-HETEROCYCLIC CARBENES; CARBON-DIOXIDE; HYDROGENATION; CONVERSION; METHANOL; EFFICIENT; HYDROFORMYLATION;
D O I
10.1016/j.checat.2023.100787
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The valorization of CO2 presents a crucial challenge in the pursuit of carbon-neutral processes. Herein, we report the successful hydroaminomethylation of diverse alkenes with CO2 and H2, using N -het-erocyclic carbene-Ru coordination assemblies as solid single-site catalysts. Intriguingly, the incorporation of imidazolium carboxylates was discovered to profoundly enhance CO2 activation, leading to excellent yields (up to 98%) and selectivity (up to 98%) toward upgraded amines across a broad substrate scope. Remarkably, a record-breaking turnover number of up to 1.8 3 104 was achieved. The robustness of the solid catalysts facilitated effortless recovery and enabled their reuse for over 10 cycles without any discernible loss in activity and selectivity, making this protocol practical and straightforward for CO2 valorization.
引用
收藏
页数:15
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