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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6331833/ https://www.ncbi.nlm.nih.gov/pubmed/26501250 http://dx.doi.org/10.3390/molecules201018856 |
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author | Mattioli, Cristina Gourdon, André |
author_facet | Mattioli, Cristina Gourdon, André |
author_sort | Mattioli, Cristina |
collection | PubMed |
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. |
format | Online Article Text |
id | pubmed-6331833 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-63318332019-01-24 Maleimides Designed for Self-Assembly and Reactivity on Graphene Mattioli, Cristina Gourdon, André Molecules Article 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. MDPI 2015-10-16 /pmc/articles/PMC6331833/ /pubmed/26501250 http://dx.doi.org/10.3390/molecules201018856 Text en © 2015 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Mattioli, Cristina Gourdon, André Maleimides Designed for Self-Assembly and Reactivity on Graphene |
title | 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_short | Maleimides Designed for Self-Assembly and Reactivity on Graphene |
title_sort | maleimides designed for self-assembly and reactivity on graphene |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6331833/ https://www.ncbi.nlm.nih.gov/pubmed/26501250 http://dx.doi.org/10.3390/molecules201018856 |
work_keys_str_mv | AT mattiolicristina maleimidesdesignedforselfassemblyandreactivityongraphene AT gourdonandre maleimidesdesignedforselfassemblyandreactivityongraphene |