Manganese catalyzed transfer hydrogenation of biomass-derived aldehydes: Insights to the catalytic performance and mechanism

被引:31
|
作者
Feng, Yunchao [1 ]
Long, Sishi [1 ]
Yan, Guihua [1 ]
Chen, Binglin [1 ]
Sperry, Jonathan [4 ]
Xu, Wanjie [5 ]
Sun, Yong [1 ,2 ,3 ]
Tang, Xing [1 ,2 ,3 ]
Zeng, Xianhai [1 ,2 ,3 ]
Lin, Lu [1 ,2 ,3 ]
机构
[1] Xiamen Univ, Coll Energy, Xiamen 361102, Peoples R China
[2] Fujian Engn & Res Ctr Clean & High Valued Technol, Xiamen 361102, Peoples R China
[3] Xiamen Key Lab Clean & High Valued Utilizat Bioma, Xiamen 361102, Peoples R China
[4] Univ Auckland, Ctr Green Chem Sci, Auckland 1142, New Zealand
[5] Xiamen Univ, Coll Mat, Xiamen 361102, Peoples R China
基金
中国国家自然科学基金;
关键词
Biomass conversion; 5-hydroxymethylfurfural; Transfer hydrogenation; Manganese hydrogenation catalysis; Mechanism study; ASYMMETRIC TRANSFER HYDROGENATION; NITROGEN-DOPED CARBON; SELECTIVE HYDROGENATION; COBALT NANOPARTICLES; FURFURYL ALCOHOL; POROUS CARBON; CONVERSION; IRON; OXIDATION; EFFICIENT;
D O I
10.1016/j.jcat.2020.05.037
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
Manganese catalyzed transfer hydrogenation (CTH) of aldehydes is an attractive method for the synthesis of alcohols. Here, we report a novel and efficient MnO@C-N catalyst for the CTH of biomass-derived 5-hydroxymethylfurfural and other aldehydes to alcohols in high yields. Catalytic experimental studies showed that the MnO and nitrogen-doping are responsible for the high selectivity and high conversion, respectively. Isotopic labelling experiments demonstrated that the CTH of aldehydes to alcohols over MnO@C-N is via a route by direct hydrogen transfer. Kinetic studies revealed that the N-doping can improve the reaction rate and reduce the activation energy of the aldehydes conversion. DFT calculations also indicated that both pyridine N and pyrrolic N doping can reduce the energy barrier for acetone desorption by the interaction between N and hydroxyl-H of alcohol. Furthermore, MnO@C-N showed good recyclability for at least five reaction cycles. We anticipate that these results can drive progress in the manganese catalyzed transfer hydrogenation reaction. (C) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页码:157 / 165
页数:9
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