Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-7060
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dc.contributor.authorTreiling, Steffen-
dc.contributor.authorWang, Cui-
dc.contributor.authorFörster, Christoph-
dc.contributor.authorReichenauer, Florian-
dc.contributor.authorKalmbach, Jens-
dc.contributor.authorBoden, Pit-
dc.contributor.authorHarris, Joe P.-
dc.contributor.authorCarrella, Luca M.-
dc.contributor.authorRentschler, Eva-
dc.contributor.authorResch-Genger, Ute-
dc.contributor.authorReber, Christian-
dc.contributor.authorSeitz, Michael-
dc.contributor.authorGerhards, Markus-
dc.contributor.authorHeinze, Katja-
dc.date.accessioned2022-06-01T09:53:35Z-
dc.date.available2022-06-01T09:53:35Z-
dc.date.issued2019-
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/7074-
dc.description.abstractPhotoactive metal complexes employing Earth-abundant metal ions are a key to sustainable photophysical and photochemical applications. We exploit the effects of an inversion center and ligand non-innocence to tune the luminescence and photochemistry of the excited state of the [CrN6] chromophore [Cr(tpe)2]3+ with close to octahedral symmetry (tpe=1,1,1-tris(pyrid-2-yl)ethane). [Cr(tpe)2]3+ exhibits the longest luminescence lifetime (τ=4500 μs) reported up to date for a molecular polypyridyl chromium(III) complex together with a very high luminescence quantum yield of Φ=8.2 % at room temperature in fluid solution. Furthermore, the tpe ligands in [Cr(tpe)2]3+ are redox non-innocent, leading to reversible reductive chemistry. The excited state redox potential and lifetime of [Cr(tpe)2]3+ surpass those of the classical photosensitizer [Ru(bpy)3]2+ (bpy=2,2′-bipyridine) enabling energy transfer (to oxygen) and photoredox processes (with azulene and tri(n-butyl)amine).en_GB
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.titleLuminescence and light-driven energy and electron transfer from an exceptionally long-lived excited state of a non-innocent chromium(III) complexen_GB
dc.typeZeitschriftenaufsatzde
dc.identifier.doihttp://doi.org/10.25358/openscience-7060-
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.titleAngewandte Chemie : International editionde
jgu.journal.volume58de
jgu.journal.issue50de
jgu.pages.start18075de
jgu.pages.end18085de
jgu.publisher.year2019-
jgu.publisher.nameWiley-VCHde
jgu.publisher.placeWeinheimde
jgu.publisher.issn1521-3773de
jgu.organisation.placeMainz-
jgu.subject.ddccode540de
jgu.publisher.doi10.1002/anie.201909325de
jgu.organisation.rorhttps://ror.org/023b0x485
Appears in collections:JGU-Publikationen

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