Exceptional chemical and thermal stability of zeolitic imidazolate frameworks

Kyo Sung Park(California NanoSystems Institute), Zheng Ni(California NanoSystems Institute), Adrien P. Côté(California NanoSystems Institute), Jae Yong Choi(Seoul National University of Education), Rudan Huang(Beijing Institute of Technology), Fernando J. Uribe‐Romo(California NanoSystems Institute), Hee K. Chae(Seoul National University of Education), M. O’Keeffe(Arizona State University), Omar M. Yaghi(California NanoSystems Institute)
Proceedings of the National Academy of Sciences
June 24, 2006
Cited by 7,365Open Access
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Abstract

Twelve zeolitic imidazolate frameworks (ZIFs; termed ZIF-1 to -12) have been synthesized as crystals by copolymerization of either Zn(II) (ZIF-1 to -4, -6 to -8, and -10 to -11) or Co(II) (ZIF-9 and -12) with imidazolate-type links. The ZIF crystal structures are based on the nets of seven distinct aluminosilicate zeolites: tetrahedral Si(Al) and the bridging O are replaced with transition metal ion and imidazolate link, respectively. In addition, one example of mixed-coordination imidazolate of Zn(II) and In(III) (ZIF-5) based on the garnet net is reported. Study of the gas adsorption and thermal and chemical stability of two prototypical members, ZIF-8 and -11, demonstrated their permanent porosity (Langmuir surface area = 1,810 m(2)/g), high thermal stability (up to 550 degrees C), and remarkable chemical resistance to boiling alkaline water and organic solvents.


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