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Stereoselective Hydrogenation of Acetylene on Copper Catalysts: A Quantum-Chemical Study Full article

Journal Kinetics and Catalysis
ISSN: 0023-1584 , E-ISSN: 1608-3210
Output data Year: 2008, Volume: 49, Number: 4, Pages: 527-530 Pages count : 4 DOI: 10.1134/S0023158408040113
Tags High Occupied Molecular Orbital; Hydrogenation Reaction; Copper Surface; Copper Particle; Copper Catalyst
Authors Zhaksibaev M.Z. 1 , Malykhin S.E. 2 , Larichev Y.V. 2 , Pak A.M. 1
Affiliations
1 Institute of Organic Catalysis and Electrochemistry, Academy of Sciences of Kazakhstan, Almaty, Kazakhstan
2 Boreskov Institute of Catalysis, Siberian Branch, Russian Academy of Sciences, Novosibirsk, 630090 Russia

Abstract: The structure of the alkyne adsorption complex on the copper surface is favorable for the stereoselective formation of cis isomers in the hydrogenation reaction. The pathway of dissociative hydrogen adsorption on copper is reported. It is assumed that the electron-donating promoter acts to reduce the electron work function of the copper catalyst by partially covering or “decorating” the surface of the copper particles.
Cite: Zhaksibaev M.Z. , Malykhin S.E. , Larichev Y.V. , Pak A.M.
Stereoselective Hydrogenation of Acetylene on Copper Catalysts: A Quantum-Chemical Study
Kinetics and Catalysis. 2008. V.49. N4. P.527-530. DOI: 10.1134/S0023158408040113 WOS Scopus РИНЦ ANCAN OpenAlex
Original: Жаксибаев М.Ж. , Малыхин С.Е. , Ларичев Ю.В. , Пак А.М.
Изучение реакции стереоселективного гидрирования ацетилена на медных катализаторах методами квантовой химии
Кинетика и катализ. 2008. Т.49. №4. С.552-555. РИНЦ
Dates:
Submitted: Sep 25, 2007
Published print: Jul 1, 2008
Published online: Aug 12, 2008
Identifiers:
Web of science: WOS:000258454900011
Scopus: 2-s2.0-49649084453
Elibrary: 13583923
Chemical Abstracts: 2008:971201
Chemical Abstracts (print): 150:143850
OpenAlex: W2043661447
Citing:
DB Citing
Web of science 1
Scopus 1
OpenAlex 1
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