Please use this identifier to cite or link to this item:
http://doi.org/10.25358/openscience-7060
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DC Field | Value | Language |
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dc.contributor.author | Treiling, Steffen | - |
dc.contributor.author | Wang, Cui | - |
dc.contributor.author | Förster, Christoph | - |
dc.contributor.author | Reichenauer, Florian | - |
dc.contributor.author | Kalmbach, Jens | - |
dc.contributor.author | Boden, Pit | - |
dc.contributor.author | Harris, Joe P. | - |
dc.contributor.author | Carrella, Luca M. | - |
dc.contributor.author | Rentschler, Eva | - |
dc.contributor.author | Resch-Genger, Ute | - |
dc.contributor.author | Reber, Christian | - |
dc.contributor.author | Seitz, Michael | - |
dc.contributor.author | Gerhards, Markus | - |
dc.contributor.author | Heinze, Katja | - |
dc.date.accessioned | 2022-06-01T09:53:35Z | - |
dc.date.available | 2022-06-01T09:53:35Z | - |
dc.date.issued | 2019 | - |
dc.identifier.uri | https://openscience.ub.uni-mainz.de/handle/20.500.12030/7074 | - |
dc.description.abstract | Photoactive 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.iso | eng | de |
dc.rights | CC BY | * |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | * |
dc.subject.ddc | 540 Chemie | de_DE |
dc.subject.ddc | 540 Chemistry and allied sciences | en_GB |
dc.title | Luminescence and light-driven energy and electron transfer from an exceptionally long-lived excited state of a non-innocent chromium(III) complex | en_GB |
dc.type | Zeitschriftenaufsatz | de |
dc.identifier.doi | http://doi.org/10.25358/openscience-7060 | - |
jgu.type.dinitype | article | en_GB |
jgu.type.version | Published version | de |
jgu.type.resource | Text | de |
jgu.organisation.department | FB 09 Chemie, Pharmazie u. Geowissensch. | de |
jgu.organisation.number | 7950 | - |
jgu.organisation.name | Johannes Gutenberg-Universität Mainz | - |
jgu.rights.accessrights | openAccess | - |
jgu.journal.title | Angewandte Chemie : International edition | de |
jgu.journal.volume | 58 | de |
jgu.journal.issue | 50 | de |
jgu.pages.start | 18075 | de |
jgu.pages.end | 18085 | de |
jgu.publisher.year | 2019 | - |
jgu.publisher.name | Wiley-VCH | de |
jgu.publisher.place | Weinheim | de |
jgu.publisher.issn | 1521-3773 | de |
jgu.organisation.place | Mainz | - |
jgu.subject.ddccode | 540 | de |
jgu.publisher.doi | 10.1002/anie.201909325 | de |
jgu.organisation.ror | https://ror.org/023b0x485 | |
Appears in collections: | JGU-Publikationen |
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File | Description | Size | Format | ||
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luminescence_and_lightdriven_-20220601114716967.pdf | 2.89 MB | Adobe PDF | View/Open |