Design and synthesis of the basic Cu-doped zeolite X catalyst with high activity in oxidative coupling reactions

被引:44
作者
Chen, Shengchun [1 ]
Shao, Zhen [1 ]
Fang, Zhongxue [1 ]
Chen, Qun [1 ]
Tang, Ting [1 ]
Fu, Wenqian [1 ]
Zhang, Lei [1 ]
Tang, Tiandi [1 ,2 ]
机构
[1] Changzhou Univ, Sch Petrochem Engn, Changzhou 213164, Jiangsu, Peoples R China
[2] Wenzhou Univ, Coll Chem & Mat Engn, Wenzhou 325035, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Cu-doped zeolite X; Lewis basicity; Oxidative coupling; Cinnamic acids; METAL-ORGANIC FRAMEWORKS; HETEROGENEOUS PALLADIUM CATALYST; MESOPOROUS SILICA; CINNAMIC-ACIDS; SUZUKI-MIYAURA; COPPER; FUNCTIONALIZATION; ALKENYLATION; ALKYLATION; CHEMISTRY;
D O I
10.1016/j.jcat.2016.01.030
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
The decarboxylative coupling of cinnamic acids with alcohols and the oxidative coupling of alkenes with aldehydes are typical organic reactions. Considering the characteristics and mechanisms of the reactions, the Cu-doped zeolite-X catalyst (Cu-X) with Lewis basic sites was synthesized and used for the two reactions. Compared with Cu, Cu2O, and CuBr2 catalysts (4-21%), the Cu-X catalyst (99%) shows extraordinary high activity in the decarboxylative coupling of cinnamic acids with alcohols. In addition, the Cu-X catalyst presents excellent performance in the oxidative coupling of alkenes with aldehydes. The strong interaction between Cu+ and the zeolite framework benefits the transformation of Cu2+ and Cu+ in the redox process, enhancing the reaction activity. More importantly, the Lewis basic sites on the Cu-X catalyst could favor the adsorption of the cinnamic acid, resulting in electron-rich density in the C=C bond, and therefore greatly improving the reaction activity. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:38 / 46
页数:9
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