Issue 17, 2019

Reaction of the C60 radical anion with alkyl halides

Abstract

The reaction of the C60 radical anion (C60˙) with α-bromo-1,3-dicarbonyl compounds selectively afforded the methanofullerene derivatives. The reaction with benzyl halide and 1,2-bis(dihalomethyl)benzene afforded the corresponding 1,4-dibenzylated C60 derivative and cycloaddition product, respectively. The possible mechanisms for the formation of the fullerene adducts are proposed.

Graphical abstract: Reaction of the C60 radical anion with alkyl halides

Supplementary files

Article information

Article type
Letter
Submitted
27 Feb 2019
Accepted
25 Mar 2019
First published
26 Mar 2019

New J. Chem., 2019,43, 6457-6460

Reaction of the C60 radical anion with alkyl halides

Y. Maeda, M. Sanno, T. Morishita, K. Sakamoto, E. Sugiyama, S. Akita, M. Yamada and M. Suzuki, New J. Chem., 2019, 43, 6457 DOI: 10.1039/C9NJ01043B

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