Highly mesoporous metal-organic framework assembled in a switchable solvent

被引:210
|
作者
Peng, Li [1 ]
Zhang, Jianling [1 ]
Xue, Zhimin [1 ]
Han, Buxing [1 ]
Sang, Xinxin [1 ]
Liu, Chengcheng [1 ]
Yang, Guanying [1 ]
机构
[1] Chinese Acad Sci, Inst Chem, CAS Key Lab Colloid Interface & Chem Thermodynam, Beijing Natl Lab Mol Sci, Beijing 100190, Peoples R China
来源
NATURE COMMUNICATIONS | 2014年 / 5卷
基金
中国国家自然科学基金;
关键词
GAS-EXPANDED LIQUIDS; X-RAY-SCATTERING; REVERSE MICELLES; COMPRESSED CO2; CATALYSIS; COORDINATION; CU-3(BTC)(2); ACTIVATION; ADSORPTION; SEPARATION;
D O I
10.1038/ncomms5465
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The mesoporous metal-organic frameworks are a family of materials that have pore sizes ranging from 2 to 50 nm, which have shown promising applications in catalysis, adsorption, chemical sensing and so on. The preparation of mesoporous metal-organic frameworks usually needs the supramolecular or cooperative template strategy. Here we report the template-free assembly of mesoporous metal-organic frameworks by using CO2-expanded liquids as switchable solvents. The mesocellular metal-organic frameworks with large mesopores (13-23 nm) are formed, and their porosity properties can be easily adjusted by controlling CO2 pressure. Moreover, the use of CO2 can accelerate the reaction for metal-organic framework formation from metal salt and organic linker due to the viscosity-lowering effect of CO2, and the product can be recovered through CO2 extraction. The as-synthesized mesocellular metal-organic frameworks are highly active in catalysing the aerobic oxidation of benzylic alcohols under mild temperature at atmospheric pressure.
引用
收藏
页数:7
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