Coupling Molecular and Nanoparticle Catalysts on Single Metal-Organic Framework Microcrystals for the Tandem Reaction of H2O2 Generation and Selective Alkene Oxidation

被引:38
作者
Limvorapitux, Rungmai [1 ]
Chou, Lien-Yang [2 ,3 ]
Young, Allison P. [2 ]
Tsung, Chia-Kuang [2 ]
Nguyen, SonBinh T. [1 ]
机构
[1] Northwestern Univ, Dept Chem, 2145 Sheridan Rd, Evanston, IL 60208 USA
[2] Boston Coll, Dept Chem, 2609 Beacon St, Chestnut Hill, MA 02467 USA
[3] ShanghaiTech Univ, Sch Phys Sci & Technol, Shanghai 201210, Peoples R China
来源
ACS CATALYSIS | 2017年 / 7卷 / 10期
基金
美国国家科学基金会;
关键词
tandem reaction; metal organic framework; in situ H2O2 generation; alkene oxidation; UiO-66; GAS-PHASE EPOXIDATION; HYDROGEN-PEROXIDE; AMBIENT-TEMPERATURE; PROPYLENE-OXIDE; LIQUID-PHASE; PD; H-2; O-2; MOF; WATER;
D O I
10.1021/acscatal.6b03632
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 molecular catalyst, (sal)Mo-VI, and a heterogeneous catalyst, either Pd or Au nanoparticles (NPs), were integrated into one UiO-66 MOF microcrystal. The resulting dually functionalized catalysts, Pd@UiO-66-(sal)Mo and Au/UiO-66-(sal)Mo, have been utilized for a one-pot tandem reaction of H2O2 generation and selective liquid-phase alkene oxidation. The NPs serve as catalysts for the production of H2O2 from H-2 and O-2 gases, while the (sal)Mo moieties function as the oxidation catalyst. When the metal NPs are fully encapsulated within the MOF microcrystals, the alkene hydrogenation side reaction is largely suppressed, with a 6-fold decrease in the hydrogenation/oxidation product ratio for 5-bromo-1-cyclooctene favoring the epoxide as the major product. For Au/UiO-66-(sal)Mo, where the two catalysts are in close proximity on the MOF microcrystal, the enhancement in oxidation productivity is increased by 10 times in comparison to the [Au/UiO-66-NR2 + UiO-66-sal(Mo)] physical mixture of the two singly functionalized MOFs.
引用
收藏
页码:6691 / 6698
页数:8
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