A novel electron Donor-Acceptor Carbazole-Zn(II)Phthalocyanine – Perfluorinated Subphthalocyanine Conjugate: synthesis, characterization, and photoinduced electron-transfer
Porphyrinoids are considered perfect candidates for the preparation of model electron donor-acceptor (D-A) systems as they enable fast and efficient photoinduced electron transfer. Herein, we report on the synthesis and photophysical characterization of a ZnPc SubPc conjugate covalently connected th...
| Autores: | , , , , , , , |
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| Tipo de recurso: | artículo |
| Fecha de publicación: | 2022 |
| País: | España |
| Institución: | Universidad Autónoma de Madrid |
| Repositorio: | Biblos-e Archivo. Repositorio Institucional de la UAM |
| Idioma: | inglés |
| OAI Identifier: | oai:repositorio.uam.es:10486/705445 |
| Acceso en línea: | http://hdl.handle.net/10486/705445 https://dx.doi.org/10.1002/cptc.202200213 |
| Access Level: | acceso abierto |
| Palabra clave: | Electron transfer Near infrared Organic photovoltaics Phthalocyanines Subphthalocyanines Química |
| Sumario: | Porphyrinoids are considered perfect candidates for the preparation of model electron donor-acceptor (D-A) systems as they enable fast and efficient photoinduced electron transfer. Herein, we report on the synthesis and photophysical characterization of a ZnPc SubPc conjugate covalently connected through a short-range alkyne spacer. We designed and prepared the conjugate, which comprise, on the one hand, a perfluorinated SubPc with strong electron acceptor character and, on the other, a Pc peripherally functionalized with carbazoles with strong electron donor character. Photoinduced electron transfer events are in-depth analyzed by several techniques, including steady-state absorption, time-resolved emission and transient absorption measurements on different time scales. Our studies confirm a full charge separation occurring from a photoexcited charge transfer state |
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