biostudies-literatureMattioli CAgence Nationale de la Recherche18856-69https://www.ebi.ac.uk/biostudies/studies/S-EPMC6331833biostudies-literatureUnknown20(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.Molecules (Basel, Switzerland)Maleimides Designed for Self-Assembly and Reactivity on Graphene.PMC6331833ANR-10-BLAN-1017 ChimiGraphNMattioli CGourdon AfalseMaleimides 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 functionalities are linked to a triethynylbenzene core.2015-01-01T00:00:00Z2015 Oct2025-04-18T15:15:40.216Z2019-03-26T22:39:27ZS-EPMC63318332650125010.3390/molecules201018856