Path Selective Photoinduced Energy and Electron Transfer in a Bis(acridinium‐Zn(II) Porphyrin)‐tetrapyridyl Porphyrin Host‐Guest Complex

The 1:1 complex of a bis(acridinium-Zn(II)porphyrin) host and a tetrapyridyl free-base porphyrin guest shows a remarkable interplay of energy and electron transfer (eT) processes, finely tuned by the solvent polarity or the selection of the photoexcited component. A more polar environment (CH<sub>2</sub>Cl<sub>2</sub>) favors uncommon parallel intramolecular and intermolecular eT processes, while in an apolar solvent (toluene) the intermolecular eT process is hampered. Notably, the apolar environment also enables a rare energy transfer process from the porphyrin guest toward the charge-transfer emissive state of the tweezer host. In total, no less than four different excited states were probed, which can be sketched by an inverted pyramid diagram highlighting directional path selection.

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Journal
Chemistry - A European Journal
Published
2025-09-19
DOI
https://doi.org/10.1002/chem.202502604
Primary Topic
Porphyrin and Phthalocyanine Chemistry
Type
article
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article

Path Selective Photoinduced Energy and Electron Transfer in a Bis(acridinium‐Zn(II) Porphyrin)‐tetrapyridyl Porphyrin Host‐Guest Complex

Barbara Ventura, Daniel Sánchez‐Resa, Daniele Veclani, Nicola Armaroli et al.
Chemistry - A European Journal
Porphyrin and Phthalocyanine Chemistry
article

Path Selective Photoinduced Energy and Electron Transfer in a Bis(acridinium‐Zn(II) Porphyrin)‐tetrapyridyl Porphyrin Host‐Guest Complex

Barbara Ventura, Daniel Sánchez‐Resa, Daniele Veclani, Nicola Armaroli, Henri‐Pierre Jacquot de Rouville, Amy Edo‐Osagie, Valérie Heitz, Federica Ruani, Andrea Barbieri, Geordie Creste
article en

Abstract

The 1:1 complex of a bis(acridinium-Zn(II)porphyrin) host and a tetrapyridyl free-base porphyrin guest shows a remarkable interplay of energy and electron transfer (eT) processes, finely tuned by the solvent polarity or the selection of the photoexcited component. A more polar environment (CH<sub>2</sub>Cl<sub>2</sub>) favors uncommon parallel intramolecular and intermolecular eT processes, while in an apolar solvent (toluene) the intermolecular eT process is hampered. Notably, the apolar environment also enables a rare energy transfer process from the porphyrin guest toward the charge-transfer emissive state of the tweezer host. In total, no less than four different excited states were probed, which can be sketched by an inverted pyramid diagram highlighting directional path selection.

Chemistry - A European JournalVol. 32(4)
Centre National de la Recherche Scientifique (FR), Institut de Chimie de Strasbourg (FR), Institute of Organic Synthesis and Photoreactivity (IT)
Openalex Percentile: Top 80%
Porphyrin and Phthalocyanine Chemistry
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