Maleimides Designed for Self-Assembly and Reactivity on Graphene

Maleimides Designed for Self-Assembly and Reactivity on Graphene

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 fun...

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Bibliographic Details
Main Authors: Cristina Mattioli, André Gourdon, NanoSciences Group
Format: Article
Language:English
Published: MDPI AG 2015-10-01
Series:Molecules
Subjects:
maleimides
Diels-Alder
graphene
Online Access:http://www.mdpi.com/1420-3049/20/10/18856
id doaj-7bcdc7794c584a6e9c035f45f8f481fd
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spelling doaj-7bcdc7794c584a6e9c035f45f8f481fd2020-11-24T22:46:08ZengMDPI AGMolecules1420-30492015-10-012010188561886910.3390/molecules201018856molecules201018856Maleimides Designed for Self-Assembly and Reactivity on GrapheneCristina Mattioli0André Gourdon1NanoSciences Group2Centre 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, FranceCentre 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, FranceCentre 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, FranceTwo 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.http://www.mdpi.com/1420-3049/20/10/18856maleimidesDiels-Aldergraphene
collection DOAJ
language English
format Article
sources DOAJ
author Cristina Mattioli
André Gourdon
NanoSciences Group
spellingShingle Cristina Mattioli
André Gourdon
NanoSciences Group
Maleimides Designed for Self-Assembly and Reactivity on Graphene
Molecules
maleimides
Diels-Alder
graphene
author_facet Cristina Mattioli
André Gourdon
NanoSciences Group
author_sort Cristina Mattioli
title Maleimides Designed for Self-Assembly and Reactivity on Graphene
title_short Maleimides Designed for Self-Assembly and Reactivity on Graphene
title_full Maleimides Designed for Self-Assembly and Reactivity on Graphene
title_fullStr Maleimides Designed for Self-Assembly and Reactivity on Graphene
title_full_unstemmed Maleimides Designed for Self-Assembly and Reactivity on Graphene
title_sort maleimides designed for self-assembly and reactivity on graphene
publisher MDPI AG
series Molecules
issn 1420-3049
publishDate 2015-10-01
description 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.
topic maleimides
Diels-Alder
graphene
url http://www.mdpi.com/1420-3049/20/10/18856
work_keys_str_mv AT cristinamattioli maleimidesdesignedforselfassemblyandreactivityongraphene
AT andregourdon maleimidesdesignedforselfassemblyandreactivityongraphene
AT nanosciencesgroup maleimidesdesignedforselfassemblyandreactivityongraphene
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