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A rare earth hydride supported ruthenium catalyst for the hydrogenation of N-heterocycles: boosting the activity via a new hydrogen transfer path and controlling the stereoselectivity

Hydrogenation of N-heterocycles is of great significance for their wide range of applications such as building blocks in drug and agrochemical syntheses and liquid organic hydrogen carriers (LOHCs). Pursuing a better hydrogenation performance and stereoselectivity, we successfully developed a rare e...

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Autores principales: Wu, Yong, Yu, Hongen, Guo, Yanru, Jiang, Xiaojing, Qi, Yue, Sun, Bingxue, Li, Haiwen, Zheng, Jie, Li, Xingguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7066573/
https://www.ncbi.nlm.nih.gov/pubmed/32190238
http://dx.doi.org/10.1039/c9sc04365a
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author Wu, Yong
Yu, Hongen
Guo, Yanru
Jiang, Xiaojing
Qi, Yue
Sun, Bingxue
Li, Haiwen
Zheng, Jie
Li, Xingguo
author_facet Wu, Yong
Yu, Hongen
Guo, Yanru
Jiang, Xiaojing
Qi, Yue
Sun, Bingxue
Li, Haiwen
Zheng, Jie
Li, Xingguo
author_sort Wu, Yong
collection PubMed
description Hydrogenation of N-heterocycles is of great significance for their wide range of applications such as building blocks in drug and agrochemical syntheses and liquid organic hydrogen carriers (LOHCs). Pursuing a better hydrogenation performance and stereoselectivity, we successfully developed a rare earth hydride supported ruthenium catalyst Ru/YH(3) for the hydrogenation of N-heterocycles, especially N-ethylcarbazole (NEC), the most promising LOHC. Full hydrogenation of NEC on Ru/YH(3) can be achieved at 363 K and 1 MPa hydrogen pressure, which is currently the lowest compared to previous reported catalysts. Furthermore, Ru/YH(3) shows the highest turnover number, namely the highest catalytic activity among the existing catalysts for hydrogenation of NEC. Most importantly, Ru/YH(3) shows remarkable stereoselectivity for all-cis products, which is very favorable for the subsequent dehydrogenation. The excellent performance of Ru/YH(3) originates from the new hydrogen transfer path from H(2) to NEC via YH(3). Ru/LaH(3) and Ru/GdH(3) also reveal good activity for hydrogenation of NEC and Ru/YH(3) also possesses good activity for hydrogenation of 2-methylindole, indicating that the use of rare earth hydride supported catalysts is a highly effective strategy for developing better hydrogenation catalysts for N-heterocycles.
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spelling pubmed-70665732020-03-18 A rare earth hydride supported ruthenium catalyst for the hydrogenation of N-heterocycles: boosting the activity via a new hydrogen transfer path and controlling the stereoselectivity Wu, Yong Yu, Hongen Guo, Yanru Jiang, Xiaojing Qi, Yue Sun, Bingxue Li, Haiwen Zheng, Jie Li, Xingguo Chem Sci Chemistry Hydrogenation of N-heterocycles is of great significance for their wide range of applications such as building blocks in drug and agrochemical syntheses and liquid organic hydrogen carriers (LOHCs). Pursuing a better hydrogenation performance and stereoselectivity, we successfully developed a rare earth hydride supported ruthenium catalyst Ru/YH(3) for the hydrogenation of N-heterocycles, especially N-ethylcarbazole (NEC), the most promising LOHC. Full hydrogenation of NEC on Ru/YH(3) can be achieved at 363 K and 1 MPa hydrogen pressure, which is currently the lowest compared to previous reported catalysts. Furthermore, Ru/YH(3) shows the highest turnover number, namely the highest catalytic activity among the existing catalysts for hydrogenation of NEC. Most importantly, Ru/YH(3) shows remarkable stereoselectivity for all-cis products, which is very favorable for the subsequent dehydrogenation. The excellent performance of Ru/YH(3) originates from the new hydrogen transfer path from H(2) to NEC via YH(3). Ru/LaH(3) and Ru/GdH(3) also reveal good activity for hydrogenation of NEC and Ru/YH(3) also possesses good activity for hydrogenation of 2-methylindole, indicating that the use of rare earth hydride supported catalysts is a highly effective strategy for developing better hydrogenation catalysts for N-heterocycles. Royal Society of Chemistry 2019-10-11 /pmc/articles/PMC7066573/ /pubmed/32190238 http://dx.doi.org/10.1039/c9sc04365a Text en This journal is © The Royal Society of Chemistry 2019 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0)
spellingShingle Chemistry
Wu, Yong
Yu, Hongen
Guo, Yanru
Jiang, Xiaojing
Qi, Yue
Sun, Bingxue
Li, Haiwen
Zheng, Jie
Li, Xingguo
A rare earth hydride supported ruthenium catalyst for the hydrogenation of N-heterocycles: boosting the activity via a new hydrogen transfer path and controlling the stereoselectivity
title A rare earth hydride supported ruthenium catalyst for the hydrogenation of N-heterocycles: boosting the activity via a new hydrogen transfer path and controlling the stereoselectivity
title_full A rare earth hydride supported ruthenium catalyst for the hydrogenation of N-heterocycles: boosting the activity via a new hydrogen transfer path and controlling the stereoselectivity
title_fullStr A rare earth hydride supported ruthenium catalyst for the hydrogenation of N-heterocycles: boosting the activity via a new hydrogen transfer path and controlling the stereoselectivity
title_full_unstemmed A rare earth hydride supported ruthenium catalyst for the hydrogenation of N-heterocycles: boosting the activity via a new hydrogen transfer path and controlling the stereoselectivity
title_short A rare earth hydride supported ruthenium catalyst for the hydrogenation of N-heterocycles: boosting the activity via a new hydrogen transfer path and controlling the stereoselectivity
title_sort rare earth hydride supported ruthenium catalyst for the hydrogenation of n-heterocycles: boosting the activity via a new hydrogen transfer path and controlling the stereoselectivity
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7066573/
https://www.ncbi.nlm.nih.gov/pubmed/32190238
http://dx.doi.org/10.1039/c9sc04365a
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