Near‐Infrared BODIPY‐Acridine Dyads Acting as Heavy‐Atom‐Free Dual‐Functioning Photosensitizers

Jasper Deckers, Tom Cardeynaels, Huguette Penxten, Anitha Ethirajan, Marcel Ameloot, Mikalai Kruk, Benoît Champagne, Wouter Maes

Résultats de recherche: Contribution à un journal/une revueArticleRevue par des pairs

Résumé

Boron dipyrromethene (BODIPY) dyes represent a particular class within the broad array of potential photosensitizers. Their highly fluorescent nature opens the door for theragnostic applications, combining imaging and therapy using a single, easily synthesized chromophore. However, near-infrared absorption is strongly desired for photodynamic therapy to enhance tissue penetration. Furthermore, singlet oxygen should preferentially be generated without the incorporation of heavy atoms, as these often require additional synthetic efforts and/or afford dark cytotoxicity. Solutions for both problems are known, but have never been successfully combined in one simple BODIPY material. Here, we present a series of compact BODIPY-acridine dyads, active in the phototherapeutic window and showing balanced brightness and phototoxic power. Although the donor–acceptor design was envisioned to introduce a charge transfer state to assist in intersystem crossing, quantum-chemical calculations refute this. Further photophysical investigations suggest the presence of exciplex states and their involvement in singlet oxygen formation.

langue originaleAnglais
Pages (de - à)15212-15225
Nombre de pages14
journalChemistry: A European Journal
Volume26
Numéro de publication66
Les DOIs
Etat de la publicationPublié - 25 juin 2020

Empreinte digitale Examiner les sujets de recherche de « Near‐Infrared BODIPY‐Acridine Dyads Acting as Heavy‐Atom‐Free Dual‐Functioning Photosensitizers ». Ensemble, ils forment une empreinte digitale unique.

Contient cette citation