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Efficient acceptorless photo-dehydrogenation of alcohols and N-heterocycles with binuclear platinum(ii) diphosphite complexes.
Zhong, Jian-Ji; To, Wai-Pong; Liu, Yungen; Lu, Wei; Che, Chi-Ming.
Afiliação
  • Zhong JJ; Department of Chemistry , Southern University of Science and Technology of China , Shenzhen , Guangdong 518055 , P. R. China.
  • To WP; Guangdong Provincial Laboratory of Chemistry and Fine Chemicals , Shantou University , Guangdong 515063 , P. R. China.
  • Liu Y; College of Chemistry and Molecular Sciences , Wuhan University Wuhan , Hubei 430072 , P. R. China.
  • Lu W; State Key Laboratory of Synthetic Chemistry , Department of Chemistry , The University of Hong Kong , Pokfulam Road , Hong Kong , P. R. China . Email: cmche@hku.hk.
  • Che CM; Department of Chemistry , Southern University of Science and Technology of China , Shenzhen , Guangdong 518055 , P. R. China.
Chem Sci ; 10(18): 4883-4889, 2019 May 14.
Article em En | MEDLINE | ID: mdl-31160960
ABSTRACT
Although photoredox catalysis employing Ru(ii) and Ir(iii) complexes as photocatalysts has emerged as a versatile tool for oxidative C-H functionalization under mild conditions, the need for additional reagents acting as electron donor/scavenger for completing the catalytic cycle undermines the practicability of this approach. Herein we demonstrate that photo-induced oxidative C-H functionalization can be catalysed with high product yields under oxygen-free and acceptorless conditions via inner-sphere atom abstraction by binuclear platinum(ii) diphosphite complexes. Both alcohols (51 examples), particularly the aliphatic ones, and saturated N-heterocycles (24 examples) can be efficiently dehydrogenated under light irradiation at room temperature. Regeneration of the photocatalyst by means of reductive elimination of dihydrogen from the in situ formed platinum(iii)-hydride species represents an alternative paradigm to the current approach in photoredox catalysis.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article