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Photoinduced energy- and electron- transfer between a photoactive cage based on a thermally activate delayed fluorescence ligand and encapsulated fluorescent dyes

Research output: Contribution to journalReview article

Author(s)

Diego Rota Martir, Antonella Pizzolante, Daniel Escudero, Denis Jacquemin, Stuart Warriner, Eli Zysman-Colman

School/Research organisations

Abstract

The vast majority of polyhedral assemblies prepared by combining organic bent ligands and “photophysically innocent” palladium(II) metal ions are non-emissive. Here we report a simple strategy to switch on the luminescence properties of a polyhedral assembly by combining a Thermally Activated Delayed Fluorescence (TADF) organic emitter based on a dipyridylcarbazole ligand scaffold with Pd2+ ions, giving rise to a luminescent Pd6L12 molecular cube. The assembly is capable of encapsulating within its cavity up to three molecules per cage of Fluorescein, in its neutral lactone form, and up to two molecules of Rose Bengal in its dianionic quinoidal form. Photoinduced electron Transfer (PeT) between the photoactive cage and the encapsulated Fluorescein and Photoinduced Energy Transfer (PET) from the cage to encapsulated Rose Bengal have been observed by steady-state and time-resolved emission spectroscopy.
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Details

Original languageEnglish
JournalACS Applied Energy Materials
VolumeIn press
Early online date11 May 2018
DOIs
Publication statusE-pub ahead of print - 11 May 2018

    Research areas

  • Photoactive cage, TADF ligand, Encapsulation of dyes, Energy and electron transfer, White-emitting assembly

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