Mixed Linker Strategies for Organic Framework Functionalization

被引:107
作者
Bunck, David N. [1 ]
Dichtel, William R. [1 ]
机构
[1] Cornell Univ, Baker Lab, Dept Chem & Chem Biol, Ithaca, NY 14853 USA
基金
美国国家科学基金会;
关键词
covalent organic frameworks; crystal engineering; functionalization; metal-organic frameworks; self-assembly; ZEOLITIC IMIDAZOLATE FRAMEWORKS; HYDROGEN STORAGE; POSTSYNTHETIC MODIFICATION; COORDINATION COPOLYMER; GAS-ADSORPTION; CARBON-DIOXIDE; SURFACE-AREA; CRYSTALLINE; DESIGN; PORE;
D O I
10.1002/chem.201203145
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Framework materials have attracted intense interest for gas storage, separations, catalysis, and other applications as a consequence of their periodicity, high specific surface area, and rational synthesis. Cocrystallizing multiple monomers with identical linking chemistry represents an emerging route to access materials with increased complexity and advanced functions. This Concept Article highlights three strategies for framework synthesis that employ mixtures of monomers with 1) identical linking geometries, 2) different linking geometries, or 3) in which one monomer is truncated with respect to the other. These approaches offer a diverse toolbox to modify framework topology, incorporate active functionality, and rationally control crystallite size and morphology.
引用
收藏
页码:818 / 827
页数:10
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