<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Tolba AH</submitter><funding>Ministerstvo Školství, Mládeže a Tělovýchovy (Ministry of Education, Youth and Sports)</funding><pagination>7851</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12373787</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(1)</volume><pubmed_abstract>In recent years, the catalytic activity of scandium triflate Sc(OTf)3 has attracted significant attention due to its robust Lewis acidity and the oxophilicity of Sc3+. These features have led to impressive progress in developing diverse organic reactions, including C-C bond formation. The Sc3+ also facilitates single electron transfer in photoinduced reactions either by coordination to an organophotoredox catalyst, which modifies its redox reactivity, or by the formation of a scandium-superoxide anion complex after electron transfer from a light-absorbing redox-active compound. The prior consideration of Sc3+ as a redox-inactive/innocent metal ion initially hampered the investigation of the possibility of using Sc(OTf)3 as a sole visible light photoredox catalyst. This work demonstrates the use of Sc(OTf)3 as a visible light photocatalyst capable of direct and mild aerobic oxidative C-H functionalisation of aromatic substrates by oxidation of the benzylic position and direct cyanation of the aromatic ring.</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Redox-innocent scandium(III) as the sole catalyst in visible light photooxidations.</pubmed_title><pmcid>PMC12373787</pmcid><funding_grant_id>CZ.02.01.01/00/22_008/0004617</funding_grant_id><funding_grant_id>INFRA CZ project (ID:90254)</funding_grant_id><pubmed_authors>Khan JI</pubmed_authors><pubmed_authors>Sturala J</pubmed_authors><pubmed_authors>El-Zohry AM</pubmed_authors><pubmed_authors>Tolba AH</pubmed_authors><pubmed_authors>Cibulka R</pubmed_authors><pubmed_authors>Pizl M</pubmed_authors><pubmed_authors>Svobodova E</pubmed_authors><pubmed_authors>Luspai K</pubmed_authors><pubmed_authors>Chudoba J</pubmed_authors><pubmed_authors>Klima J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Redox-innocent scandium(III) as the sole catalyst in visible light photooxidations.</name><description>In recent years, the catalytic activity of scandium triflate Sc(OTf)3 has attracted significant attention due to its robust Lewis acidity and the oxophilicity of Sc3+. These features have led to impressive progress in developing diverse organic reactions, including C-C bond formation. The Sc3+ also facilitates single electron transfer in photoinduced reactions either by coordination to an organophotoredox catalyst, which modifies its redox reactivity, or by the formation of a scandium-superoxide anion complex after electron transfer from a light-absorbing redox-active compound. The prior consideration of Sc3+ as a redox-inactive/innocent metal ion initially hampered the investigation of the possibility of using Sc(OTf)3 as a sole visible light photoredox catalyst. This work demonstrates the use of Sc(OTf)3 as a visible light photocatalyst capable of direct and mild aerobic oxidative C-H functionalisation of aromatic substrates by oxidation of the benzylic position and direct cyanation of the aromatic ring.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Aug</publication><modification>2026-05-08T06:51:27.764Z</modification><creation>2026-04-07T23:31:06.16Z</creation></dates><accession>S-EPMC12373787</accession><cross_references><pubmed>40846847</pubmed><doi>10.1038/s41467-025-63233-4</doi></cross_references></HashMap>