Fe‐Co Alloyed Nanoparticles Catalyzing Efficient Hydrogenation of Cinnamaldehyde to Cinnamyl Alcohol in Water

Selective hydrogenation of C=O against the conjugated C=C in cinnamaldehyde (CAL) is indispensable to produce cinnamyl alcohol (COL). Nonetheless, it is challenged by the low selectivity and the need to use organic solvents. Herein, for the first time, we report the use of Fe‐Co alloy nanoparticles...

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Published inAngewandte Chemie International Edition Vol. 59; no. 52; pp. 23521 - 23526
Main Authors Lv, Yang, Han, Miaomiao, Gong, Wanbing, Wang, Dongdong, Chen, Chun, Wang, Guozhong, Zhang, Haimin, Zhao, Huijun
Format Journal Article
LanguageEnglish
Published Germany Wiley Subscription Services, Inc 21.12.2020
EditionInternational ed. in English
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Summary:Selective hydrogenation of C=O against the conjugated C=C in cinnamaldehyde (CAL) is indispensable to produce cinnamyl alcohol (COL). Nonetheless, it is challenged by the low selectivity and the need to use organic solvents. Herein, for the first time, we report the use of Fe‐Co alloy nanoparticles (NPs) on N‐doped carbon support as a selective hydrogenation catalyst to efficiently convert CAL to COL. The resultant catalyst with the optimized Fe/Co ratio of 0.5 can achieve an exceptional COL selectivity of 91.7 % at a CAL conversion of 95.1 % in pure water medium under mild reaction conditions, ranking it the best performed catalyst reported to date. The experimental results confirm that the COL selectivity and CAL conversion efficiency are, respectively promoted by the presence of Fe and Co, while the synergism of the alloyed Fe‐Co is the key to concurrently achieve high COL selectivity and CAL conversion efficiency. A bimetallic Fe‐Co alloying strategy is innovatively utilized to concurrently enhance the selectivity and conversion efficiency for selective hydrogenation of cinnamaldehyde to cinnamyl alcohol in water. A Fe‐Co alloy catalyst with a Fe/Co molar ratio of 0.5 achieves an exceptional selectivity of 91.7 % at 95.1 % conversion.
Bibliography:These authors contributed equally to this work.
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ISSN:1433-7851
1521-3773
DOI:10.1002/anie.202009913