TY - JOUR
T1 - Selective Hydrodeoxygenation of Aromatics to Cyclohexanols over Ru Single Atoms Supported on CeO2
AU - Zhang, Kaili
AU - Meng, Qinglei
AU - Wu, Haihong
AU - Yan, Jiang
AU - Mei, Xuelei
AU - An, Pengfei
AU - Zheng, Lirong
AU - Zhang, Jing
AU - He, Mingyuan
AU - Han, Buxing
N1 - Publisher Copyright:
© 2022 American Chemical Society.
PY - 2022/11/16
Y1 - 2022/11/16
N2 - Cyclohexanols are widely used chemicals, which are mainly produced by oxidation of fossil feedstocks. Selective hydrodeoxygenation of lignin derivatives has great potential for producing these chemicals but is challenging to obtain high yields. Here, we report that CeO2-supported Ru single-atom catalysts (SACs) enabled the hydrogenation of the benzene ring and catalyzed etheric C-O(R) bond cleavage without changing the C-O(H) bond, which could afford 99.9% yields of cyclohexanols. As far as we know, this is the first to report that SACs catalyze hydrogenation of the aromatic ring. The reaction mechanism was studied by control experiments and density functional theory calculations. In the catalysts, the Ru-O-Ce sites were formed and one Ru atom was coordinated with about four O atoms. These catalytic sites could realize both the hydrogenation and deoxygenation reactions efficiently, and thus desired cyclohexanols were generated. This work pioneers the single-atom catalysis in aromatic transformation and provides a novel route for synthesis of cyclohexanols.
AB - Cyclohexanols are widely used chemicals, which are mainly produced by oxidation of fossil feedstocks. Selective hydrodeoxygenation of lignin derivatives has great potential for producing these chemicals but is challenging to obtain high yields. Here, we report that CeO2-supported Ru single-atom catalysts (SACs) enabled the hydrogenation of the benzene ring and catalyzed etheric C-O(R) bond cleavage without changing the C-O(H) bond, which could afford 99.9% yields of cyclohexanols. As far as we know, this is the first to report that SACs catalyze hydrogenation of the aromatic ring. The reaction mechanism was studied by control experiments and density functional theory calculations. In the catalysts, the Ru-O-Ce sites were formed and one Ru atom was coordinated with about four O atoms. These catalytic sites could realize both the hydrogenation and deoxygenation reactions efficiently, and thus desired cyclohexanols were generated. This work pioneers the single-atom catalysis in aromatic transformation and provides a novel route for synthesis of cyclohexanols.
UR - https://www.scopus.com/pages/publications/85141723605
U2 - 10.1021/jacs.2c08992
DO - 10.1021/jacs.2c08992
M3 - 文章
C2 - 36332192
AN - SCOPUS:85141723605
SN - 0002-7863
VL - 144
SP - 20834
EP - 20846
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 45
ER -