Exploitation of Intrinsic Microporosity in Polymer-Based Materials

被引:705
作者
McKeown, Neil B. [1 ]
Budd, Peter M. [2 ]
机构
[1] Cardiff Univ, Sch Chem, Cardiff CF10 3AT, S Glam, Wales
[2] Univ Manchester, Sch Chem, Manchester M13 9PL, Lancs, England
基金
英国工程与自然科学研究理事会;
关键词
PORE-SIZE DISTRIBUTION; MOLECULARLY IMPRINTED POLYMERS; COVALENT ORGANIC FRAMEWORKS; FREE-VOLUME DISTRIBUTION; SI(CH3)(3) SIDE-GROUPS; HIGH-SURFACE-AREA; HYDROGEN STORAGE; GAS SEPARATION; POTENTIAL ADSORBENTS; NANOPOROUS POLYMERS;
D O I
10.1021/ma1006396
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The past decade has seen the development of microporous materials (i.e., materials containing pores of dimensions < 2 nm) derived wholly from organic components. Here we review this nascent area with a particular emphasis on amorphous polymers that possess intrinsic microporosity (IM), which is defined as microporosity that arises directly from the shape and rigidity of component macromolecules. Although IM can be readily identified within soluble non-network polymers and oligomers, for network polymers it is harder to differentiate IM from template effects that are responsible for the microporosity within hyper-cross-linked networks. The numerous examples of microporous polymers assembled from rigid monomers by the formation of rigid linking groups are surveyed and their IM assessed. The potential applications of these materials are highlighted.
引用
收藏
页码:5163 / 5176
页数:14
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