Turning the product selectivity of nitrile hydrogenation from primary to secondary amines by precise modification of Pd/SiC catalysts using NiO nanodots-Reference-Cited by-同舟云学术

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Turning the product selectivity of nitrile hydrogenation from primary to secondary amines by precise modification of Pd/SiC catalysts using NiO nanodots

Published:2019 Issue:9 Volume:9 Page:2266-2272
ISSN:2044-4753
Container-title:Catalysis Science & Technology
language:en
Short-container-title:Catal. Sci. Technol.

Author:

Jiao Zhi-Feng¹²³⁴⁵,Zhao Ji-Xiao¹²³⁴⁵,Guo Xiao-Ning⁶⁷⁸⁹¹⁰,Tong Xi-Li¹²³⁴,Zhang Bin¹²³⁴^ORCID,Jin Guo-Qiang¹²³⁴,Qin Yong¹²³⁴⁵^ORCID,Guo Xiang-Yun¹²³⁴⁵^ORCID

Affiliation:

1. State Key Laboratory of Coal Conversion

2. Institute of Coal Chemistry, Chinese Academy of Sciences

3. Taiyuan 030001

4. China

5. Center of Materials Science and Optoelectronics Engineering

6. Institut für Anorganische Chemie

7. and Institute for Sustainable Chemistry & Catalysis with Boron

8. Julius-Maximilians-Universität Würzburg

9. 97074 Würzburg

10. Germany

Abstract

The selectivity of nitrile hydrogenation was turned by the concentration of hydrogen radicals on Pd surface.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2019/CY/C9CY00353C

Reference51 articles.

1. Amines: Synthesis, Properties and Application , ed. S. A. Lawrence , Cambridge University Press , Cambridge , 2004

2. Tandem Catalysis of Amines Using Porous Graphene Oxide

3. Homogeneous Hydrogenations of Nitriles Catalyzed by Rhenium Complexes

4. Synthesis of secondary amines

5. Cesium Hydroxide Promoted Chemoselective N-Alkylation for the Generally Efficient Synthesis of Secondary Amines

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