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A series of potent BODIPY photosensitisers featuring tellurophene motifs at boron.
Campbell, Jacob W; Tung, Matthew T; Taylor, Breanna B; Beharry, Andrew A; Thompson, Alison.
Afiliação
  • Campbell JW; Department of Chemistry, Dalhousie University, Halifax, Nova Scotia, B3H 4J3, Canada.
  • Tung MT; Department of Chemistry and Physical Sciences, University of Toronto, Mississauga, Ontario, L5L 1C6, Canada. andrew.beharry@utoronto.ca.
  • Taylor BB; Department of Chemistry, Dalhousie University, Halifax, Nova Scotia, B3H 4J3, Canada.
  • Beharry AA; Department of Chemistry and Physical Sciences, University of Toronto, Mississauga, Ontario, L5L 1C6, Canada. andrew.beharry@utoronto.ca.
  • Thompson A; Department of Chemistry, Dalhousie University, Halifax, Nova Scotia, B3H 4J3, Canada.
Org Biomol Chem ; 22(20): 4157-4162, 2024 May 22.
Article em En | MEDLINE | ID: mdl-38715527
ABSTRACT
This article describes the synthesis and photophysical properties of a series of BODIPY photosensitisers that feature tellurophene motifs appended at the boron centre. These compounds were obtained via nucleophilic substitution of various F-BODIPYs with lithiated tellurophene. The synthetic scope, photophysical characteristics and photosensitisation properties are discussed. Structural modifications around the BODIPY core resulted in an eight-fold improvement in light IC50 values compared to previous designs.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Biomol Chem Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Biomol Chem Ano de publicação: 2024 Tipo de documento: Article