Issue 19, 2001
From the journal:

Chemical Communications

First synthesis of a highly symmetrical decakis-adduct of fullerene dimer C120

Koichi Fujiwaraa  and  Koichi Komatsu*a  

* Corresponding authors

a Institute for Chemical Research, Kyoto University, Uji, Kyoto, Japan.
E-mail: komatsu@scl.kyoto-u.ac.jp;
Fax: +81 774 38 3178;
Tel: +81 774 38 3172

Abstract

The highly symmetrical decakis-cyclopropanated derivative of C120 was synthesized using template activation and the structure was determined by X-ray crystallography; the decakis-adduct was converted into the eicosa-carboxylic acid derivative that is water soluble.

Graphical abstract: First synthesis of a highly symmetrical decakis-adduct of fullerene dimer C120

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Article information

DOI
https://doi.org/10.1039/B105191C
Article type
Communication
Submitted
25 Jun 2001
Accepted
29 Aug 2001
First published
10 Sep 2001

Chem. Commun., 2001, 1986-1987

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First synthesis of a highly symmetrical decakis-adduct of fullerene dimer C120

K. Fujiwara and K. Komatsu, Chem. Commun., 2001, 1986 DOI: 10.1039/B105191C

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