Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.


Science 14 January 2005:
Vol. 307. no. 5707, pp. 238 - 240
DOI: 10.1126/science.1106185

Reports

Encapsulation of Molecular Hydrogen in Fullerene C60 by Organic Synthesis

Koichi Komatsu,* Michihisa Murata, Yasujiro Murata

In spite of their importance in fundamental and applied studies, the preparation of endohedral fullerenes has relied on difficult-to-control physical methods. We report a four-step organic reaction that completely closes a 13-membered ring orifice of an open-cage fullerene. This process can be used to synthesize a fullerene C60 encapsulating molecular hydrogen, which can be isolated as a pure product. This molecular surgical method should make possible the preparation of a series of C60 fullerenes, encapsulating either small atoms or molecules, that are not accessible by conventional physical methods.

Institute for Chemical Research, Kyoto University, Uji, Kyoto 611-0011, Japan.

* To whom correspondence should be addressed. E-mail: komatsu{at}scl.kyoto-u.ac.jp

Read the Full Text





To Advertise     Find Products


Science. ISSN 0036-8075 (print), 1095-9203 (online)