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A general approach to non-fullerene electron acceptors based on the corannulene motif

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dc.contributor.authorBarat, Viktor-
dc.contributor.authorBudanovic, Maja-
dc.contributor.authorHalilovic, Dzeneta-
dc.contributor.authorHuh, June-
dc.contributor.authorWebster, Richard D.-
dc.contributor.authorMahadevegowda, Surendra H.-
dc.contributor.authorStuparu, Mihaiela C.-
dc.date.accessioned2021-09-01T17:20:20Z-
dc.date.available2021-09-01T17:20:20Z-
dc.date.created2021-06-18-
dc.date.issued2019-03-14-
dc.identifier.issn1359-7345-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/66669-
dc.description.abstractHere, we show that oxidation of exo-cyclic sulfur atoms enhances the molecular reduction potential of non-planar polycyclic aromatic hydrocarbons and allows for a systematic bridging of the electron affinity gap between corannulene, a fragment of fullerene C-60, and the prevalent fullerene-based electron acceptor phenyl-C-61-butyric acid methyl ester (PCBM).-
dc.languageEnglish-
dc.language.isoen-
dc.publisherROYAL SOC CHEMISTRY-
dc.subjectDERIVATIVES-
dc.subjectBUCKYBOWLS-
dc.titleA general approach to non-fullerene electron acceptors based on the corannulene motif-
dc.typeArticle-
dc.contributor.affiliatedAuthorHuh, June-
dc.identifier.doi10.1039/c9cc00327d-
dc.identifier.scopusid2-s2.0-85062596078-
dc.identifier.wosid000460731900015-
dc.identifier.bibliographicCitationCHEMICAL COMMUNICATIONS, v.55, no.21, pp.3113 - 3116-
dc.relation.isPartOfCHEMICAL COMMUNICATIONS-
dc.citation.titleCHEMICAL COMMUNICATIONS-
dc.citation.volume55-
dc.citation.number21-
dc.citation.startPage3113-
dc.citation.endPage3116-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusDERIVATIVES-
dc.subject.keywordPlusBUCKYBOWLS-
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