Bioinspired Metal-Organic Framework Catalysts for Selective Methane Oxidation to Methanol

被引:388
作者
Baek, Jayeon [1 ,2 ,3 ,4 ]
Rungtaweevoranit, Bunyarat [1 ,2 ,3 ,5 ]
Pei, Xiaokun [1 ,2 ,3 ,5 ]
Park, Myeongkee [7 ]
Fakra, Sirine C. [6 ]
Liu, Yi-Sheng [6 ]
Matheu, Roc [1 ,2 ,3 ,5 ]
Alshmimri, Sultan A. [8 ]
Alshehri, Saeed [8 ]
Trickett, Christopher A. [1 ,2 ,3 ,5 ]
Somorjai, Gabor A. [1 ,4 ,5 ]
Yaghi, Omar M. [1 ,2 ,3 ,5 ]
机构
[1] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Kavli Energy NanoSci Inst Berkeley, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Berkeley Global Sci Inst, Berkeley, CA 94720 USA
[4] Lawrence Berkeley Natl Lab, Chem Sci Div, Berkeley, CA 94720 USA
[5] Lawrence Berkeley Natl Lab, Mat Sci Div, Berkeley, CA 94720 USA
[6] Lawrence Berkeley Natl Lab, Adv Light Source, Berkeley, CA 94720 USA
[7] Dong A Univ, Dept Chem, Coll Nat Sci, Busan 49315, South Korea
[8] King Abdulaziz City Sci & Technol, Riyadh 12354, Saudi Arabia
关键词
RAY-ABSORPTION SPECTROSCOPY; ACTIVE-SITE; K-EDGE; OXO-CLUSTERS; COPPER; COMPLEXES; OXYGEN; BIS(MU-OXO)DICOPPER; CONVERSION; REACTIVITY;
D O I
10.1021/jacs.8b11525
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Particulate methane monooxygenase (pMMO) is an enzyme that oxidizes methane to methanol with high activity and selectivity. Limited success has been achieved in incorporating biologically relevant ligands for the formation of such active site in a synthetic system. Here, we report the design and synthesis of metal-organic framework (MOF) catalysts inspired by pMMO for selective methane oxidation to methanol. By judicious selection of a framework with appropriate topology and chemical functionality, MOF-808 was used to postsynthetically install ligands bearing imidazole units for subsequent metalation with Cu(I) in the presence of dioxygen. The catalysts show high selectivity for methane oxidation to methanol under isothermal conditions at 150 degrees C. Combined spectroscopies and density functional theory calculations suggest bis(mu-oxo) dicopper species as probable active site of the catalysts.
引用
收藏
页码:18208 / 18216
页数:9
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