Issue 99, 2014

NBS-promoted oxidation of fullerene monoradicals leading to regioselective 1,4-difunctional fullerenes

Abstract

We have demonstrated that NBS is able to promote the oxidation of fullerene monoradicals to form 1,4-difunctional fullerenes. The singly bonded fullerene dimers were used as fullerene monoradical precursors, which produced various 1,4-fullerenes with a wide range of functional groups in good to high yields with high regioselectivity in terms of cosolvents and nucleophiles.

Graphical abstract: NBS-promoted oxidation of fullerene monoradicals leading to regioselective 1,4-difunctional fullerenes

Supplementary files

Article information

Article type
Communication
Submitted
02 Oct 2014
Accepted
27 Oct 2014
First published
27 Oct 2014

Chem. Commun., 2014,50, 15730-15732

Author version available

NBS-promoted oxidation of fullerene monoradicals leading to regioselective 1,4-difunctional fullerenes

W. Si, S. Lu, N. Asao, M. Bao, Y. Yamamoto and T. Jin, Chem. Commun., 2014, 50, 15730 DOI: 10.1039/C4CC07780F

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