BODIPYs have a well-established role in biological sciences as chemosensors and versatile biological markers due to their chemical reactivity, which allows for fine-tuning of their photophysical characteristics. In this work, we combined the unique reactivity of arylazo sulfones with the advantages of a “sunflow” reactor to develop a fast, efficient, and versatile method for the photochemical arylation of BODIPYs and other chromophores. This approach resulted in red-shifted emitting fluorophores due to extended electronic delocalization at the 3- and 5-positions of the BODIPY core. This method represents an advantageous approach for BODIPY functionalization compared to existing strategies.

Versatile Metal-Free Arylation of BODIPY and Bis(BF2) Chromophores by Using Arylazosulfones in a Sunflow System

Protti S.;
2024-01-01

Abstract

BODIPYs have a well-established role in biological sciences as chemosensors and versatile biological markers due to their chemical reactivity, which allows for fine-tuning of their photophysical characteristics. In this work, we combined the unique reactivity of arylazo sulfones with the advantages of a “sunflow” reactor to develop a fast, efficient, and versatile method for the photochemical arylation of BODIPYs and other chromophores. This approach resulted in red-shifted emitting fluorophores due to extended electronic delocalization at the 3- and 5-positions of the BODIPY core. This method represents an advantageous approach for BODIPY functionalization compared to existing strategies.
2024
Chemistry & Analysis
Esperti anonimi
Inglese
Internazionale
30
61
Arylation; Arylazosulfones; BIS(BF; 2; ) chromophores; BODIPY; Sunflow
9
info:eu-repo/semantics/article
262
de Melo, S. M. G.; dos Santos, T.; Silva, D. G.; Martins, Y. A.; Eckhardt, P.; Lopez, R. F. V.; Opatz, T.; Protti, S.; da Silva Emery, F.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/1510075
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