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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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Publication details

The article was received on 07 Apr 2012, accepted on 16 May 2012 and first published on 17 May 2012


Article type: Communication
DOI: 10.1039/C2CC32517A
Citation: Chem. Commun., 2012,48, 7158-7160
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    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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