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Photoinduced Electron Transfer in Clicked Ferrocene-BODIPY-Fullerene Conjugates

  • Jad Rabah
  • , Anam Fatima
  • , Hélène Fensterbank
  • , Karen Wright
  • , Anne Vallée
  • , Maïssa Gueye
  • , Gotard Burdzinski
  • , Gilles Clavier
  • , Fabien Miomandre
  • , Julie Pham
  • , Michel Sliwa
  • , Rachel Méallet-Renault
  • , Karine Steenkeste
  • , Thomas Pino
  • , Minh Huong Ha-Thi
  • , Emmanuel Allard
  • Institut Lavoisier de Versailles
  • Universite Paris-Sud
  • Adam Mickiewicz University/Faculty of Biology
  • ENS Paris-Saclay
  • Laboratoire de Spectrochimie Infrarouge et Raman, Université des Sciences et Technologies de Lille, UMR-CNRS 8516

Research output: Contribution to journalArticlepeer-review

Abstract

Ferrocene-BODIPY (Fc-BDP) conjugates in which one or two ferrocene entities are linked to the β-positions of the BODIPY core by an ethynyl bridge have been developed. These derivatives were easily and efficiently grafted onto a dual-clickable fullerene platform using CuAAC reactions, leading to a clickable Fc-BDP-C60 triad and a clickable [Fc]2-BDP-C60 tetrad which can be used for further derivatization with complex structures. Due to the extended π-conjugation and the presence of an intramolecular charge transfer band from Fc to BDP, all these conjugates display a broad absorption in the visible region, which is bathochromically shifted when two Fc are appended to the BDP core. Ultrafast multistep electron transfers leading to charge stabilization were demonstrated in the Fc-BDP-C60 triad and [Fc]2-BDP-C60 tetrad by femtosecond transient absorption studies.

Original languageEnglish
Article numbere202300039
JournalHelvetica Chimica Acta
Volume106
Issue number6
DOIs
Publication statusPublished - 1 Jun 2023
Externally publishedYes

Keywords

  • CuAAC reaction
  • boron dipyrromethenes
  • donor-acceptor systems
  • electron transfer
  • ferrocene, fullerenes

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