Litcius/Paper detail

Metallaphotoredox C−O and C−N Cross‐Coupling Using Donor‐Acceptor Cyanoarene Photocatalysts

Tommaso Gandini, Luigi Dolcini, Lorenzo Di Leo, Matthieu Fornara, Alberto Bossi, Marta Penconi, Alberto Dal Corso, Cesare Gennari, Luca Pignataro

2022ChemCatChem17 citationsDOIOpen Access PDF

Abstract

Abstract Herein we report a study on the use of donor‐acceptor cyanoarenes as photocatalysts for C−O and C−N coupling reactions promoted by nickel. We found that some of these stable and readily available organic compounds can replace the precious metal photocatalysts originally employed in these methodologies. After reaction optimization, the application scope of the best performing dyes was investigated and found to cover several nucleophiles (alcohols and amines) and aryl bromides. Control experiments, fluorescence quenching studies and examination of yield trends suggest that both etherification and amination probably proceed via a dark Ni I /Ni III ‐catalytic cycle initiated and sustained by a photoredox cycle involving the organic photocatalysts.

Topics & Concepts

AminationNucleophileChemistryAcceptorArylCatalysisCatalytic cycleQuenching (fluorescence)NickelPhotochemistryYield (engineering)Organic synthesisCoupling reactionCombinatorial chemistryFluorescenceOrganic chemistryMaterials scienceQuantum mechanicsAlkylPhysicsMetallurgyCondensed matter physicsRadical Photochemical ReactionsSulfur-Based Synthesis TechniquesCatalytic C–H Functionalization Methods
Metallaphotoredox C−O and C−N Cross‐Coupling Using Donor‐Acceptor Cyanoarene Photocatalysts | Litcius