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Superior Metal-Organic Framework Activation with Dimethyl Ether
被引:13
|作者:
Wright, Keenan R.
[3
]
Nath, Karabi
[3
]
Matzger, Adam J.
[1
,2
,3
]
机构:
[1] Univ Michigan, Dept Chem & Macromol Sci, 930 North Univ Ave, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Engn Program, 930 North Univ Ave, Ann Arbor, MI 48109 USA
[3] Inst Univ Michigan, Dept Chem, 930 North Univ Ave, Ann Arbor, MI 48109 USA
基金:
美国能源部;
关键词:
Coordination Chemistry;
Metal-Organic Frameworks;
Microporous Materials;
Structural Collapse;
Surface Area;
MICROPOROUS COORDINATION POLYMERS;
VAPOR-PRESSURE MEASUREMENTS;
CARBON-DIOXIDE;
SURFACE-AREAS;
PURIFICATION;
PERFORMANCE;
ADSORPTION;
CAPACITY;
STORAGE;
DESIGN;
D O I:
10.1002/anie.202213190
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Metal-organic frameworks (MOFs) are demonstrated to be readily activated by treatment with the low surface tension, low boiling point solvent dimethyl ether (DME). The mildness of the method enables access to high surface areas by avoiding structural changes in the framework that often plague thermal activation methods. A distinction from previous methods is that DME activation succeeds for materials with coordinatively unsaturated sites (CUS) and non-CUS MOFs as well. DME displaces solvent molecules occupying the pores of the MOF as well as those coordinated to metal centers; reducing evacuation temperature by using a coordinating, yet highly volatile guest enables low temperature activation with structural retention as demonstrated surface area measurements that match or exceed existing activation protocols.
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