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dc.contributor.authorMaulbetsch, Theo
dc.contributor.authorFrech, Philipp
dc.contributor.authorScheele, Marcus
dc.contributor.authorTörnroos, Karl Wilhelm
dc.contributor.authorKunz, Doris
dc.date.accessioned2023-10-10T12:41:49Z
dc.date.available2023-10-10T12:41:49Z
dc.date.created2023-09-28T08:50:06Z
dc.date.issued2023
dc.identifier.issn0947-6539
dc.identifier.urihttps://hdl.handle.net/11250/3095527
dc.description.abstractWe present the synthesis of a new type of an expanded porphyrinoid macrocycle with a saddle-shaped morphology and its complexation of C60 guest molecules. The new macrocycle contains four carbazole and four triazole moieties and can be readily synthesized via a copper-catalyzed click reaction. It shows specific photo-physical properties including fluorescence with a high quantum yield of 60 %. The combination of the saddle-shaped geometry with the expanded π-system allows for host–guest interactions with C60 in a stacked polymer fashion. Evidence for the presence of a host–guest complex is provided both in solution by NMR spectroscopy and in the solid state by X-ray structure analysis.en_US
dc.language.isoengen_US
dc.publisherWileyen_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.no*
dc.titleA Saddle-Shaped Expanded Porphyrinoid Fitting C60**en_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2023 The Author(s)en_US
dc.source.articlenumbere202302104en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.doi10.1002/chem.202302104
dc.identifier.cristin2179680
dc.source.journalChemistry - A European Journalen_US
dc.identifier.citationChemistry - A European Journal. 2023, e202302104.en_US


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Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal
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