Issue 11, 2013

Mechanochemically driven solid-state Diels–Alder reaction of graphite into graphene nanoplatelets

Abstract

A mechanochemically driven solid-state Diels–Alder reaction is demonstrated via dry ball-milling graphite as the diene in the presence of maleic anhydride or maleimide as the dienophile. On the basis of various characterizations, the Diels–Alder adducts are edge-selectively functionalized and subsequently delaminated into graphene nanoplatelets.

Graphical abstract: Mechanochemically driven solid-state Diels–Alder reaction of graphite into graphene nanoplatelets

Supplementary files

Article information

Article type
Edge Article
Submitted
02 Jun 2013
Accepted
14 Aug 2013
First published
16 Aug 2013

Chem. Sci., 2013,4, 4273-4277

Mechanochemically driven solid-state Diels–Alder reaction of graphite into graphene nanoplatelets

J. Seo, I. Jeon and J. Baek, Chem. Sci., 2013, 4, 4273 DOI: 10.1039/C3SC51546J

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