Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-9153
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dc.contributor.authorSittel, Steven-
dc.contributor.authorSell, Arne Christian-
dc.contributor.authorHofmann, Kamil-
dc.contributor.authorWiedemann, Christina-
dc.contributor.authorNau, Jan Philipp-
dc.contributor.authorKerzig, Christoph-
dc.contributor.authorManolikakes, Georg-
dc.contributor.authorHeinze, Katja-
dc.date.accessioned2023-06-07T10:07:51Z-
dc.date.available2023-06-07T10:07:51Z-
dc.date.issued2023-
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/9170-
dc.description.abstractIncorporation of sulfur dioxide into organic compounds is achieved by a photocatalytic approach using sensitizers made from earth-abundant chromium(III) ions and visible light leading to sulfones and sulfonamides. We employed three different chromium(III) sensitizers [Cr(ddpd)2]3+, [Cr(bpmp)2]3+ and [Cr(tpe)2]3+ with long excited state lifetimes and different ground and excited state redox potentials as well as varying stability under the reaction conditions (ddpd=N,N’-dimethyl-N,N’-dipyridin-2-yl-pyridine-2,6-diamine; bpmp=2,6-bis(2-pyridylmethyl)pyridine; tpe=1,1,1-tris(pyrid-2-yl)ethane). Key reaction steps of the catalytic cycles are identified by electrochemical, luminescence quenching, photolysis, laser flash photolysis and catalytic experiments delivering a detailed picture of the challenges in these transformations. The reactivity of the reduced chromium complex was identified as a key property to explain the reaction outcomes. Initial cage escape yield determinations with [Cr(tpe)2]3+ revealed that desired photoreactions occur with unusually high quantum efficiencies, whereas side reactions are almost unproductive.en_GB
dc.language.isoengde
dc.rightsCC BY-NC*
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/*
dc.subject.ddc540 Chemiede_DE
dc.subject.ddc540 Chemistry and allied sciencesen_GB
dc.titleVisible-light induced fixation of SO2 into organic molecules with polypyridine chromium(III) complexesen_GB
dc.typeZeitschriftenaufsatzde
dc.identifier.doihttp://doi.org/10.25358/openscience-9153-
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.titleChemCatChemde
jgu.journal.volume15de
jgu.journal.issue6de
jgu.pages.alternativee202201562de
jgu.publisher.year2023-
jgu.publisher.nameWiley-VCHde
jgu.publisher.placeWeinheimde
jgu.publisher.issn1867-3899de
jgu.organisation.placeMainz-
jgu.subject.ddccode540de
jgu.publisher.doi10.1002/cctc.202201562de
jgu.organisation.rorhttps://ror.org/023b0x485-
Appears in collections:DFG-491381577-H

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