{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Mattioli C"],"funding":["Agence Nationale de la Recherche"],"pagination":["18856-69"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC6331833"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["20(10)"],"pubmed_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."],"journal":["Molecules (Basel, Switzerland)"],"pubmed_title":["Maleimides Designed for Self-Assembly and Reactivity on Graphene."],"pmcid":["PMC6331833"],"funding_grant_id":["ANR-10-BLAN-1017 ChimiGraphN"],"pubmed_authors":["Mattioli C","Gourdon A"],"additional_accession":[]},"is_claimable":false,"name":"Maleimides Designed for Self-Assembly and Reactivity on Graphene.","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.","dates":{"release":"2015-01-01T00:00:00Z","publication":"2015 Oct","modification":"2025-04-18T15:15:40.216Z","creation":"2019-03-26T22:39:27Z"},"accession":"S-EPMC6331833","cross_references":{"pubmed":["26501250"],"doi":["10.3390/molecules201018856"]}}