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Science 18 November 2005:
Vol. 310. no. 5751, pp. 1166 - 1170
DOI: 10.1126/science.1120411

Reports

Porous, Crystalline, Covalent Organic Frameworks

Adrien P. Côté,1* Annabelle I. Benin,1 Nathan W. Ockwig,1 Michael O'Keeffe,2 Adam J. Matzger,1 Omar M. Yaghi1*

Covalent organic frameworks (COFs) have been designed and successfully synthesized by condensation reactions of phenyl diboronic acid {C6H4[B(OH)2]2} and hexahydroxytriphenylene [C18H6(OH)6]. Powder x-ray diffraction studies of the highly crystalline products (C3H2BO)6·(C9H12)1 (COF-1) and C9H4BO2 (COF-5) revealed expanded porous graphitic layers that are either staggered (COF-1, P63/mmc) or eclipsed (COF-5, P6/mmm). Their crystal structures are entirely held by strong bonds between B, C, and O atoms to form rigid porous architectures with pore sizes ranging from 7 to 27 angstroms. COF-1 and COF-5 exhibit high thermal stability (to temperatures up to 500° to 600°C), permanent porosity, and high surface areas (711 and 1590 square meters per gram, respectively).

1 Materials Design and Discovery Group, Department of Chemistry, University of Michigan, 930 North University Avenue, Ann Arbor, MI 48109–1055, USA.
2 Department of Chemistry and Biochemistry, Arizona State University, Tempe, AZ 85287–1604, USA.

* To whom correspondence should be addressed. E-mail: oyaghi{at}umich.edu (O.M.Y.); apcote{at}umich.edu (A.P.C.)

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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Designed Synthesis of 3D Covalent Organic Frameworks.
H. M. El-Kaderi, J. R. Hunt, J. L. Mendoza-Cortes, A. P. Cote, R. E. Taylor, M. O'Keeffe, and O. M. Yaghi (2007)
Science 316, 268-272
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Science. ISSN 0036-8075 (print), 1095-9203 (online)