Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-8311
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dc.contributor.authorKitzmann, Winald R.-
dc.contributor.authorHeinze, Katja-
dc.date.accessioned2023-02-09T09:28:12Z-
dc.date.available2023-02-09T09:28:12Z-
dc.date.issued2022-
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/8327-
dc.description.abstractTransition metal complexes with photoactive chargetransfer excited states are pervasive throughout literature. Especially [Ru(bpy) 3 ] 2+ (bpy = 2,2’-bipyridine) with its long-lived triplet metal-toligand charge-transfer emission has been established as a key model complex in the past decades. Meanwhile, interest in luminescence and reactivity of so-called spin-flip metal-centered states has risen dramatically after the Molecular Ruby [Cr(ddpd) 2 ] 3+ (ddpd = N , N ’dimethyl- N , N ’-dipyridin-2-yl-pyridine-2,6-diamine) unveiled design principles to access strong, long-lived emission from photostable chromium(III) complexes. This review contrasts the properties of emissive charge-transfer and spin-flip states illustrated with the prototypical complexes [Ru(bpy) 3 ] 2+ and [Cr(ddpd) 2 ] 3+ . First, we discuss the nature of the relevant excited states, their tunability with regards to energy and lifetime, and their responses to external stimuli. The final section identifies strengths and weaknesses of the charge transfer and spin-flip states in applications such as photoredox catalysis, sensing and circularly polarized luminescence (CPL).en_GB
dc.description.sponsorshipGefördert durch die Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 491381577de
dc.language.isoengde
dc.rightsCC BY-NC-ND*
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.ddc540 Chemiede_DE
dc.subject.ddc540 Chemistry and allied sciencesen_GB
dc.titleCharge-transfer and spin-flip states : thriving as complementsen_GB
dc.typeZeitschriftenaufsatzde
dc.identifier.doihttp://doi.org/10.25358/openscience-8311-
jgu.type.contenttypeScientific articlede
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.volumeVersion of Record (VoR)de
jgu.pages.alternativee202213207de
jgu.publisher.year2022-
jgu.publisher.nameWiley-VCHde
jgu.publisher.placeWeinheimde
jgu.publisher.issn1521-3773de
jgu.organisation.placeMainz-
jgu.subject.ddccode540de
jgu.publisher.doi10.1002/anie.202213207de
jgu.organisation.rorhttps://ror.org/023b0x485-
jgu.subject.dfgNaturwissenschaftende
jgu.relation.IsVersionOf10.25358/openscience-10133-
Appears in collections:DFG-491381577-H

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