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Maleimides Designed for Self-Assembly and Reactivity on Graphene.

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.

SUBMITTER: Mattioli C 

PROVIDER: S-EPMC6331833 | biostudies-other | 2015 Oct

REPOSITORIES: biostudies-other

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Maleimides Designed for Self-Assembly and Reactivity on Graphene.

Mattioli Cristina C   Gourdon André A  

Molecules (Basel, Switzerland) 20151016 10

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. ...[more]

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