多孔性
微型多孔材料
材料科学
共价键
多孔介质
化学工程
笼子
纳米技术
催化作用
复合材料
化学
有机化学
数学
组合数学
工程类
作者
Tomokazu Tozawa,James T. A. Jones,S.I. Swamy,Shan Jiang,Dave J. Adams,Stephen Shakespeare,Rob Clowes,Darren Bradshaw,Tom Hasell,Samantha Y. Chong,Chiu C. Tang,Stephen P. Thompson,Julia E. Parker,Abbie Trewin,John Bacsa,Alexandra M. Z. Slawin,Alexander Steiner,Andrew I. Cooper
出处
期刊:Nature Materials
[Springer Nature]
日期:2009-10-25
卷期号:8 (12): 973-978
被引量:1032
摘要
Porous materials are important in a wide range of applications including molecular separations and catalysis. We demonstrate that covalently bonded organic cages can assemble into crystalline microporous materials. The porosity is prefabricated and intrinsic to the molecular cage structure, as opposed to being formed by non-covalent self-assembly of non-porous sub-units. The three-dimensional connectivity between the cage windows is controlled by varying the chemical functionality such that either non-porous or permanently porous assemblies can be produced. Surface areas and gas uptakes for the latter exceed comparable molecular solids. One of the cages can be converted by recrystallization to produce either porous or non-porous polymorphs with apparent Brunauer-Emmett-Teller surface areas of 550 and 23 m2 g(-1), respectively. These results suggest design principles for responsive porous organic solids and for the modular construction of extended materials from prefabricated molecular pores.
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