Mesoporous H-ZSM-5 nanocrystals with programmable number of acid sites as "solid ligands" to activate Pd nanoparticles for C-C coupling reactions

被引:25
作者
Ke, Wenyu [1 ]
Cui, Tianlu [1 ]
Yu, Qiuying [1 ]
Wang, Mengying [1 ]
Lv, Libing [1 ]
Wang, Honghui [1 ]
Jiang, Zhidong [1 ]
Li, Xinhao [1 ]
Chen, Jiesheng [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Chem & Chem Engn, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
Bronsted acidity; palladium; HZSM-5; mesopores; Suzuki coupling; SILICALITE-1; ZEOLITE; CARBON; TEMPERATURE; SELECTIVITY; REDUCTION; CATALYSIS; FRAMEWORK; EFFICIENT; SUPPORTS; G-C3N4;
D O I
10.1007/s12274-017-1698-9
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
In this work, we described a proof-of-concept method to promote the activity and selectivity of Pd nanoparticles for heterogeneous catalysis (exemplified by C-C coupling reactions) by using acid sites within a zeolite framework. The Pd nanoparticles were encapsulated inside the crystalline walls of mesoporous H-ZSM-5 leading to hybrid samples (denoted as Pd@mZ-x-H) with controlled number of acid sites. A linear relationship between the number of acid sites of the zeolite nanocrystals and the catalytic activities of the Pd nanoparticles in organic reactions was established. Moreover, the shape-dependent selectivity of Pd@mZ-x-H was not sacrificed when the final activity was enhanced.
引用
收藏
页码:874 / 881
页数:8
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