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Redox-innocent scandium(III) as the sole catalyst in visible light photooxidations.


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.

SUBMITTER: Tolba AH 

PROVIDER: S-EPMC12373787 | biostudies-literature | 2025 Aug

REPOSITORIES: biostudies-literature

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Redox-innocent scandium(III) as the sole catalyst in visible light photooxidations.

Tolba Amal Hassan AH   El-Zohry Ahmed M AM   Khan Jafar Iqbal JI   Svobodová Eva E   Chudoba Josef J   Klíma Jiří J   Lušpai Karol K   Pižl Martin M   Šturala Jiří J   Cibulka Radek R  

Nature communications 20250822 1


In recent years, the catalytic activity of scandium triflate Sc(OTf)<sub>3</sub> has attracted significant attention due to its robust Lewis acidity and the oxophilicity of Sc<sup>3+</sup>. These features have led to impressive progress in developing diverse organic reactions, including C-C bond formation. The Sc<sup>3+</sup> also facilitates single electron transfer in photoinduced reactions either by coordination to an organophotoredox catalyst, which modifies its redox reactivity, or by the f  ...[more]

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