Enhancement of the catalytic activity of Suzuki coupling reactions by reduction of modified carriers and promotion of Pd/H2-PrxOy surface electron transfer
Author:
Affiliation:
1. College of Chemical Engineering, Inner Mongolia University of Technology, Hohhot, 010051, People's Republic of China
2. Inner Mongolia Key Laboratory of Industrial Catalysis, Hohhot, 010051, People's Republic of China
Abstract
Funder
Natural Science Foundation of Inner Mongolia
Publisher
Royal Society of Chemistry (RSC)
Subject
Materials Chemistry,General Chemistry,Catalysis
Link
http://pubs.rsc.org/en/content/articlepdf/2022/NJ/D2NJ02830A
Reference47 articles.
1. 9-Arylacenaphtho[1,2-b]quinoxalines via Suzuki coupling reaction as cancer therapeutic and cellular imaging agents
2. Synthesis, characterization and biological activities of 3-aryl-1,4-naphthoquinones – green palladium-catalysed Suzuki cross coupling
3. Synthesis of BiarylsviaLigand-Free Suzuki-Miyaura Cross-Coupling Reactions: A Review of Homogeneous and Heterogeneous Catalytic Developments
4. Graphene-How a Laboratory Curiosity Suddenly Became Extremely Interesting
5. Pd nanoparticle supported reduced graphene oxide and its excellent catalytic activity for the Ullmann C–C coupling reaction in a green solvent
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1. Spin–orbit coupling of electrons on separate lanthanide atoms of Pr2O2 and its singly charged cation;The Journal of Chemical Physics;2023-12-22
2. Photoactive mesoporous magnetic nanocomposite of TiO2-Pd for a clean and sustainble Suzuki-Miyaura cross-coupling reaction via blue-LED and Mott-Schottky effect;Molecular Catalysis;2023-11
3. Schiff base modified starch: A promising biosupport for palladium in Suzuki cross-coupling reactions;International Journal of Biological Macromolecules;2023-04
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