Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-9522
Full metadata record
DC FieldValueLanguage
dc.contributor.authorRocker, Johannes-
dc.contributor.authorDresel, Johannes A.-
dc.contributor.authorKrieger, Leonie A.-
dc.contributor.authorEckhardt, Paul-
dc.contributor.authorOrtuño, Ana M.-
dc.contributor.authorKitzmann, Winald R.-
dc.contributor.authorClever, Guido H.-
dc.contributor.authorHeinze, Katja-
dc.contributor.authorOpatz, Till-
dc.date.accessioned2023-09-12T08:15:33Z-
dc.date.available2023-09-12T08:15:33Z-
dc.date.issued2023-
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/9540-
dc.description.abstractA series of substituted derivatives of tetraaza[7]helicenes were synthesized and the influence of the substitution on their photophysical and photoredox-catalytic properties was studied. The combination of their high fluorescence quantum yields of up to 0.65 and their circularly polarized luminescence (CPL) activity results in CPL brightness values (BCPL) that are among the highest recorded for [7]helicenes so far. A sulfonylation/hetarylation reaction using cyanopyridines as substrates for photoinduced electron transfer (PET) from the excited helicenes was conducted to test for viability in photoredox catalysis. DFT calculations predict the introduction of electron withdrawing substituents to yield more oxidizing catalysts.en_GB
dc.description.sponsorshipDeutsche Forschungsgemeinschaft (DFG)|491381577|Open-Access-Publikationskosten 2022–2024 Universität Mainz - Universitätsmedizin-
dc.language.isoengde
dc.rightsCC BY*
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/*
dc.subject.ddc540 Chemiede_DE
dc.subject.ddc540 Chemistry and allied sciencesen_GB
dc.titleSubstitution effects on the photophysical and photoredox properties of tetraaza[7]helicenesen_GB
dc.typeZeitschriftenaufsatzde
dc.identifier.doihttp://doi.org/10.25358/openscience-9522-
jgu.type.dinitypearticleen_GB
jgu.type.versionPublished versionde
jgu.type.resourceTextde
jgu.organisation.departmentFB 09 Chemie, Pharmazie u. Geowissensch.de
jgu.organisation.number7950-
jgu.organisation.nameJohannes Gutenberg-Universität Mainz-
jgu.rights.accessrightsopenAccess-
jgu.journal.titleChemistry - a European journalde
jgu.journal.volume29de
jgu.journal.issue48de
jgu.pages.alternativee202301244de
jgu.publisher.year2023-
jgu.publisher.nameWiley-VCHde
jgu.publisher.placeWeinheimde
jgu.publisher.issn1521-3765de
jgu.organisation.placeMainz-
jgu.subject.ddccode540de
jgu.publisher.doi10.1002/chem.202301244de
jgu.organisation.rorhttps://ror.org/023b0x485-
jgu.subject.dfgLebenswissenschaftende
Appears in collections:DFG-491381577-H

Files in This Item:
  File Description SizeFormat
Thumbnail
substitution_effects_on_the_p-20230901152129218.pdf2.62 MBAdobe PDFView/Open