Design and preparation of a simple and effective palladium catalyst and the hydrogenation performance toward dibenzylbiotinmethylester

被引:4
|
作者
An, Nihong [1 ]
Dai, Yunsheng [1 ]
Tang, Chun [1 ]
Yuan, Xiaoling [2 ]
Dong, Jilong [1 ]
Shen, Yafeng [1 ]
Zhou, Wei [1 ]
机构
[1] Kunming Inst Precious Met, Sino Platinum Met Co Ltd, State Key Lab Adv Technol Comprehens Utilizat Pla, Kunming 650106, Peoples R China
[2] Jilin Univ, Coll Chem, State Key Lab Theoret & Computat Chem, Changchun 130021, Peoples R China
基金
中国博士后科学基金;
关键词
Palladium catalyst; Metal-support interaction; Functionalization; Hydrogenation; AQUEOUS-PHASE HYDROGENATION; FORMIC-ACID OXIDATION; PD/C CATALYSTS; GAMMA-BUTYROLACTONE; CARBON MATERIALS; NANOPARTICLES; SURFACE; SELECTIVITY; MWCNT; HYDRODECHLORINATION;
D O I
10.1016/j.jcis.2016.01.066
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A series of well-dispersed carbon supported Pd catalysts were prepared by a simple and effective method under mild conditions. The functionalized carbon supported Pd catalyst (Pd/AC-H) demonstrated a enhanced performance to original carbon supported Pd catalyst (Pd/AC) in the probe reaction hydrogenation of 3,4-(1',3'-Dibenzy1-2'-oxoimidazolido)-2-(4-carboxybutylidene)thiophane to dibenzylbiotinmethylester. The results of various characterization techniques revealed that the improvement of Pd dispersion on Pd/AC-H catalyst surface could be associated to the presence of abundant oxygen containing groups available for anchorage. Furthermore, the role of the surface groups of carbon supports was indispensable since they could provide an efficient pathway for the reaction. The oxygen-containing groups located at the Pd-supports interface were able to adjust the strength of reactant adsorption/activation on the Pd active sites, which was responsible for the high yield of dibenzylbiotinmethylester. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:56 / 61
页数:6
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