Hydrogen Auto‐transfer Synthesis of Quinoxalines from o‐Nitroanilines and Biomass‐based Diols Catalyzed by MOF‐derived N,P Co‐doped Cobalt Catalysts

A Co‐based heterogeneous catalyst supported on N,P co‐doped porous carbon (Co@NCP) is prepared via a facile in‐situ doping‐carbonization method. The Co@NCP composite features a large surface area, high pore volume, high‐density and strong basic sites. Furthermore, doping of P atoms can regulate the...

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Published inChemCatChem Vol. 13; no. 1; pp. 373 - 381
Main Authors Sun, Kangkang, Li, Dandan, Lu, Guo‐Ping, Cai, Chun
Format Journal Article
LanguageEnglish
Published Weinheim Wiley Subscription Services, Inc 12.01.2021
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Abstract A Co‐based heterogeneous catalyst supported on N,P co‐doped porous carbon (Co@NCP) is prepared via a facile in‐situ doping‐carbonization method. The Co@NCP composite features a large surface area, high pore volume, high‐density and strong basic sites. Furthermore, doping of P atoms can regulate the electronic density of Co. Therefore, Co@NCP exhibits good performance for the synthesis of quinoxalines from o‐nitroanilines and biomass‐derived diols under alkali‐free conditions. Heterogeneous catalysis: The synthesis of a Co‐based heterogeneous catalyst supported on N,P co‐doped porous carbon (Co@NCP) by a facile in‐situ doping‐carbonization method is reported. Co@NCP exhibits good performance for the synthesis of quinoxalines from o‐nitroanilines and biomass‐derived diols under alkali‐free conditions.
AbstractList A Co‐based heterogeneous catalyst supported on N,P co‐doped porous carbon (Co@NCP) is prepared via a facile in‐situ doping‐carbonization method. The Co@NCP composite features a large surface area, high pore volume, high‐density and strong basic sites. Furthermore, doping of P atoms can regulate the electronic density of Co. Therefore, Co@NCP exhibits good performance for the synthesis of quinoxalines from o‐nitroanilines and biomass‐derived diols under alkali‐free conditions. Heterogeneous catalysis: The synthesis of a Co‐based heterogeneous catalyst supported on N,P co‐doped porous carbon (Co@NCP) by a facile in‐situ doping‐carbonization method is reported. Co@NCP exhibits good performance for the synthesis of quinoxalines from o‐nitroanilines and biomass‐derived diols under alkali‐free conditions.
A Co‐based heterogeneous catalyst supported on N,P co‐doped porous carbon (Co@NCP) is prepared via a facile in‐situ doping‐carbonization method. The Co@NCP composite features a large surface area, high pore volume, high‐density and strong basic sites. Furthermore, doping of P atoms can regulate the electronic density of Co. Therefore, Co@NCP exhibits good performance for the synthesis of quinoxalines from o‐nitroanilines and biomass‐derived diols under alkali‐free conditions.
A Co‐based heterogeneous catalyst supported on N,P co‐doped porous carbon (Co@NCP) is prepared via a facile in‐situ doping‐carbonization method. The Co@NCP composite features a large surface area, high pore volume, high‐density and strong basic sites. Furthermore, doping of P atoms can regulate the electronic density of Co. Therefore, Co@NCP exhibits good performance for the synthesis of quinoxalines from o ‐nitroanilines and biomass‐derived diols under alkali‐free conditions.
Author Lu, Guo‐Ping
Sun, Kangkang
Cai, Chun
Li, Dandan
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Snippet A Co‐based heterogeneous catalyst supported on N,P co‐doped porous carbon (Co@NCP) is prepared via a facile in‐situ doping‐carbonization method. The Co@NCP...
A Co‐based heterogeneous catalyst supported on N,P co‐doped porous carbon (Co@NCP) is prepared via a facile in‐situ doping‐carbonization method. The Co@NCP...
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SubjectTerms Atomic properties
Biomass
Catalysts
Density
Diols
Doping
heterogeneous cobalt catalyst
hydrogen auto-transfer
in-situ doping-carbonization
N,P co-doped carbon
Quinoxalines
Title Hydrogen Auto‐transfer Synthesis of Quinoxalines from o‐Nitroanilines and Biomass‐based Diols Catalyzed by MOF‐derived N,P Co‐doped Cobalt Catalysts
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fcctc.202001362
https://www.proquest.com/docview/2477693320
Volume 13
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