Please use this identifier to cite or link to this item: https://physrep.ff.bg.ac.rs/handle/123456789/1299
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dc.contributor.authorMitrović, Aleksandraen
dc.contributor.authorTodorović, Ninaen
dc.contributor.authorŽekić, Andrijanaen
dc.contributor.authorStanković, Daliboren
dc.contributor.authorMilić, Draganaen
dc.contributor.authorMaslak, Veselinen
dc.date.accessioned2022-09-06T07:50:54Z-
dc.date.available2022-09-06T07:50:54Z-
dc.date.issued2013-04-01en
dc.identifier.issn1434-193Xen
dc.identifier.urihttps://physrep.ff.bg.ac.rs/handle/123456789/1299-
dc.description.abstractA series of novel fulleropyrrolidine–phthalimide dyads was synthesized and their electrochemical and self-assembly properties were investigated. Efficient synthesis of acceptor– acceptor dyads was performed under microwave irradiation. Fine-tuning of the second redox potentials in the dyads was achieved by varying the length of the aliphatic spacer (C2 to C12) between the fulleropyrrolidine and phthalimide moieties. Shape-shifting and supramolecular polymorphism were observed for these compounds during self-assembly.en
dc.relation.ispartofEuropean Journal of Organic Chemistryen
dc.subjectCyclic voltammetryen
dc.subjectDyadsen
dc.subjectElectrochemistryen
dc.subjectFullerenesen
dc.subjectMicrowave chemistryen
dc.subjectPolymorphismen
dc.titleSynthesis, electrochemistry, and hierarchical self-organization of fulleropyrrolidine–phthalimide dyadsen
dc.typeArticleen
dc.identifier.doi10.1002/ejoc.201201631en
dc.identifier.scopus2-s2.0-84887621810en
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/84887621810en
dc.relation.issue11en
dc.relation.volume2013en
dc.relation.firstpage2188en
dc.relation.lastpage2193en
item.openairetypeArticle-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
crisitem.author.orcid0000-0001-7720-5846-
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