Ultrahigh Porosity in Metal-Organic Frameworks

Author:

Furukawa Hiroyasu1,Ko Nakeun2,Go Yong Bok1,Aratani Naoki1,Choi Sang Beom2,Choi Eunwoo1,Yazaydin A. Özgür3,Snurr Randall Q.3,O’Keeffe Michael1,Kim Jaheon2,Yaghi Omar M.14

Affiliation:

1. Center for Reticular Chemistry at the California NanoSystems Institute, and Department of Chemistry and Biochemistry, University of California Los Angeles (UCLA), 607 Charles E. Young Drive East, Los Angeles, CA 90095, USA.

2. Department of Chemistry, Soongsil University, Seoul 156-743, Korea.

3. Department of Chemical and Biological Engineering, Northwestern University, Evanston, IL 60208, USA.

4. UCLA–Department of Energy (DOE) Institute of Genomics and Proteomics, UCLA, 607 Charles E. Young Drive East, Los Angeles, CA 90095, USA.

Abstract

Network Approaches to Highly Porous Materials Metal-organic frameworks (MOFs), in which inorganic centers are bridged by organic linkers, can achieve very high porosity for gas absorption. However, as the materials develop larger void spaces, there is also more room for growing interpenetrating networks—filling the open spaces not with gas molecules but with more MOFs. Furukawa et al. (p. 424 , published online 1 July) describe the synthesis of a MOF in which zinc centers are bridged with long, highly conjugated organic linkers, but in which the overall symmetry of the networks created prevents formation of interpenetrating networks. Extremely high surface areas and storage capacities for hydrogen, carbon dioxide, and methane were observed.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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