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Issue 57, 2012
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Highly selective reactions of C60Cl6 with thiols for the synthesis of functionalized [60]fullerene derivatives

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Abstract

Chlorofullerene C60Cl6 undergoes highly selective reactions with thiols forming compounds C60[SR]5H with high yields. These reactions open up straightforward synthetic routes to many functionalized fullerene derivatives, e.g. water-soluble compounds showing interesting biological activities.

Graphical abstract: Highly selective reactions of C60Cl6 with thiols for the synthesis of functionalized [60]fullerene derivatives

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Article information


Submitted
07 Apr 2012
Accepted
16 May 2012
First published
17 May 2012

Chem. Commun., 2012,48, 7158-7160
Article type
Communication

Highly selective reactions of C60Cl6 with thiols for the synthesis of functionalized [60]fullerene derivatives

E. A. Khakina, A. A. Yurkova, A. S. Peregudov, S. I. Troyanov, V. V. Trush, A. I. Vovk, A. V. Mumyatov, V. M. Martynenko, J. Balzarini and P. A. Troshin, Chem. Commun., 2012, 48, 7158
DOI: 10.1039/C2CC32517A

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