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.

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

Bossi Alberto;Penconi Marta;
2022

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.
2022
Istituto di Scienze e Tecnologie Chimiche "Giulio Natta" - SCITEC
metallaphotoredox catalysis
nickel
donor-acceptor cyanoarenes
cross-coupling
organic dyes
File in questo prodotto:
File Dimensione Formato  
prod_478372-doc_195980.pdf

solo utenti autorizzati

Descrizione: articolo
Tipologia: Versione Editoriale (PDF)
Licenza: NON PUBBLICO - Accesso privato/ristretto
Dimensione 6.38 MB
Formato Adobe PDF
6.38 MB Adobe PDF   Visualizza/Apri   Richiedi una copia
29 2022 Chem Cat Chem ESI.pdf

accesso aperto

Descrizione: Supporting Information
Tipologia: Versione Editoriale (PDF)
Licenza: Altro tipo di licenza
Dimensione 5.21 MB
Formato Adobe PDF
5.21 MB Adobe PDF Visualizza/Apri
Manuscript_REVISED 14-10-2022.pdf

Open Access dal 12/10/2023

Tipologia: Documento in Post-print
Licenza: Altro tipo di licenza
Dimensione 1.15 MB
Formato Adobe PDF
1.15 MB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/458880
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 11
  • ???jsp.display-item.citation.isi??? 11
social impact