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Carbonaceous materials as catalyst supports for the enantioselective hydrogenation of (E)-alpha-phenylcinnamic acid: Effect of the support acidity

Authors
Trung, Tran Si BuiKim, YeonwooKang, SunghoKim, SehunLee, Hangil
Issue Date
Sep-2015
Publisher
ELSEVIER SCIENCE BV
Keywords
Carbonaceous materials; Activated carbon; Graphene oxide; Carbon nanotubes; Deposition method; Pd-based catalysts; (E)-alpha-phenylcinnamic acid; Asymmetric hydrogenation
Citation
APPLIED CATALYSIS A-GENERAL, v.505, pp 319 - 325
Pages
7
Journal Title
APPLIED CATALYSIS A-GENERAL
Volume
505
Start Page
319
End Page
325
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/10237
DOI
10.1016/j.apcata.2015.08.011
ISSN
0926-860X
1873-3875
Abstract
A systematic comparative study of carbonaceous materials as catalyst supports for the asymmetric heterogeneous hydrogenation of (E)-alpha-phenylcinnamic acid (PCA) was performed to investigate the influence of the supports on the enantioselectivity. A series of Pd-based catalysts supported on activated carbon (AC), graphene oxide (GO), or carbon nanotubes (CNTs) was prepared using deposition methods. The hydrogenation reactions of PCA were conducted with/without the pretreatment of the prepared catalysts, and the results showed a significant drop of enantiomeric excess (ee) when the Pd/GO catalyst was used (27%) compared to that obtained from the Pd/AC (70%) and Pd/CNTs (66%) catalysts. This drop of ee values was assigned to the abundance of acidic sites present on the Pd/GO catalyst, as revealed by TGA, FT-IR, and TPD-NH3 analyses. The effect of the support acidity on the ee was ascribed to the preferential adsorption mode of cinchonidine (CD) on the GO surface via electrostatic interactions between the negatively charged oxygen functional groups present on the GO surface and the positively protonated amine groups of the CD molecule. (C) 2015 Elsevier B.V. All rights reserved.
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