BODIPY‐Perylene Charge Transfer Compounds; Sensitizers for Triplet‐Triplet Annihilation Up‐conversion

Author:

Arellano‐Reyes Ruben Arturo1,Prabhakaran Amrutha1,Sia Rengel Cane E.2,Guthmuller Julien2,Jha Keshav Kumar34,Yang Tingxiang34,Dietzek‐Ivanšić Benjamin34,McKee Vickie5,Keyes Tia E.1ORCID

Affiliation:

1. School of Chemical Sciences National Centre for Sensor Research Dublin City University Glasnevin Dublin 9 Ireland

2. Institute of Physics and Applied Computer Science Faculty of Applied Physics and Mathematics Gdańsk University of Technology Narutowicza 11/12 80233 Gdańsk Poland

3. Leibniz Institute of Photonic Technology Jena (IPHT) Department Functional Interfaces Albert-Einstein-Straße 9 07745 Jena Germany

4. Institute of Physical Chemistry Friedrich Schiller University elmholtzweg 4 07743 Jena Germany

5. Department of Physics Chemistry and Pharmacy University of Southern Denmark Campusvej 55 5230 Odense M Denmark

Abstract

AbstractBODIPY heterochromophores, asymmetrically substituted with perylene and/or iodine at the 2 and 6 positions were prepared and investigated as sensitizers for triplet‐triplet annihilation up conversion (TTA‐UC). Single‐crystal X‐ray crystallographic analyses show that the torsion angle between BODIPY and perylene units lie between 73.54 and 74.51, though they are not orthogonal. Both compounds show intense, charge transfer absorption and emission profiles, confirmed by resonance Raman spectroscopy and consistent with DFT calculations. The emission quantum yield was solvent dependent but the emission profile remained characteristic of CT transition across all solvents explored. Both BODIPY derivatives were found to be effective sensitizers of TTA‐UC with perylene annihilator in dioxane and DMSO. Intense anti‐Stokes emission was observed, and visible by eye from these solvents. Conversely, no TTA‐UC was observed from the other solvents explored, including from non‐polar solvents such as toluene and hexane that yielded brightest fluorescence from the BODIPY derivatives. In dioxane, the power density plots obtained were strongly consistent with TTA‐UC and the power density threshold, the Ith value (the photon flux at which 50 % of ΦTTAUC is achieved), for B2PI was observed to be 2.5x lower than of B2P under optimal conditions, an effect ascribed to the combined influence of spin‐orbit charge transfer intersystem crossing (SOCT‐ISC) and heavy metal on the triplet state formation for B2PI.

Funder

H2020 Marie Skłodowska-Curie Actions

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

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