Maleimides Designed for Self-Assembly and Reactivity on GrapheneReport as inadecuate

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Centre d’Elaboration de Matériaux et d’Etudes Structurales, Centre National de la Recherche Scientifique, CEMES-CNRS, 29 rue Jeanne Marvig, BP 94347, 31055, Toulouse Cedex 4, France

These authors contributed equally to this work.


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Academic Editor: Derek J. McPhee

Abstract Two new maleimide derivatives have been synthesized, prone to self-assemble and react with graphene as dienophiles. Both compounds bear a long alkyl chain on the carbon-carbon double bond position 3. The maleimide 1 bears a second alkyl chain at the nitrogen, while in compound 2, three maleimide functionalities are linked to a triethynylbenzene core. View Full-Text

Keywords: maleimides; Diels-Alder; graphene maleimides; Diels-Alder; graphene

Author: Cristina Mattioli †, André Gourdon †,* and NanoSciences Group



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