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Synthesis, Photophysical and Electronic Properties of New Red‐to‐NIR Emitting Donor–Acceptor Pyrene Derivatives

We synthesized new pyrene derivatives with strong bis(para‐methoxyphenyl)amine donors at the 2,7‐positions and n‐azaacene acceptors at the K‐region of pyrene. The compounds possess a strong intramolecular charge transfer, leading to unusual properties such as emission in the red to NIR region (700 n...

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Autores principales: Merz, Julia, Dietz, Maximilian, Vonhausen, Yvonne, Wöber, Frederik, Friedrich, Alexandra, Sieh, Daniel, Krummenacher, Ivo, Braunschweig, Holger, Moos, Michael, Holzapfel, Marco, Lambert, Christoph, Marder, Todd B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6973242/
https://www.ncbi.nlm.nih.gov/pubmed/31593316
http://dx.doi.org/10.1002/chem.201904219
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author Merz, Julia
Dietz, Maximilian
Vonhausen, Yvonne
Wöber, Frederik
Friedrich, Alexandra
Sieh, Daniel
Krummenacher, Ivo
Braunschweig, Holger
Moos, Michael
Holzapfel, Marco
Lambert, Christoph
Marder, Todd B.
author_facet Merz, Julia
Dietz, Maximilian
Vonhausen, Yvonne
Wöber, Frederik
Friedrich, Alexandra
Sieh, Daniel
Krummenacher, Ivo
Braunschweig, Holger
Moos, Michael
Holzapfel, Marco
Lambert, Christoph
Marder, Todd B.
author_sort Merz, Julia
collection PubMed
description We synthesized new pyrene derivatives with strong bis(para‐methoxyphenyl)amine donors at the 2,7‐positions and n‐azaacene acceptors at the K‐region of pyrene. The compounds possess a strong intramolecular charge transfer, leading to unusual properties such as emission in the red to NIR region (700 nm), which has not been reported before for monomeric pyrenes. Detailed photophysical studies reveal very long intrinsic lifetimes of >100 ns for the new compounds, which is typical for 2,7‐substituted pyrenes but not for K‐region substituted pyrenes. The incorporation of strong donors and acceptors leads to very low reduction and oxidation potentials, and spectroelectrochemical studies show that the compounds are on the borderline between localized Robin‐Day class‐II and delocalized Robin‐Day class‐III species.
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spelling pubmed-69732422020-01-27 Synthesis, Photophysical and Electronic Properties of New Red‐to‐NIR Emitting Donor–Acceptor Pyrene Derivatives Merz, Julia Dietz, Maximilian Vonhausen, Yvonne Wöber, Frederik Friedrich, Alexandra Sieh, Daniel Krummenacher, Ivo Braunschweig, Holger Moos, Michael Holzapfel, Marco Lambert, Christoph Marder, Todd B. Chemistry Full Papers We synthesized new pyrene derivatives with strong bis(para‐methoxyphenyl)amine donors at the 2,7‐positions and n‐azaacene acceptors at the K‐region of pyrene. The compounds possess a strong intramolecular charge transfer, leading to unusual properties such as emission in the red to NIR region (700 nm), which has not been reported before for monomeric pyrenes. Detailed photophysical studies reveal very long intrinsic lifetimes of >100 ns for the new compounds, which is typical for 2,7‐substituted pyrenes but not for K‐region substituted pyrenes. The incorporation of strong donors and acceptors leads to very low reduction and oxidation potentials, and spectroelectrochemical studies show that the compounds are on the borderline between localized Robin‐Day class‐II and delocalized Robin‐Day class‐III species. John Wiley and Sons Inc. 2019-11-19 2020-01-07 /pmc/articles/PMC6973242/ /pubmed/31593316 http://dx.doi.org/10.1002/chem.201904219 Text en © 2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full Papers
Merz, Julia
Dietz, Maximilian
Vonhausen, Yvonne
Wöber, Frederik
Friedrich, Alexandra
Sieh, Daniel
Krummenacher, Ivo
Braunschweig, Holger
Moos, Michael
Holzapfel, Marco
Lambert, Christoph
Marder, Todd B.
Synthesis, Photophysical and Electronic Properties of New Red‐to‐NIR Emitting Donor–Acceptor Pyrene Derivatives
title Synthesis, Photophysical and Electronic Properties of New Red‐to‐NIR Emitting Donor–Acceptor Pyrene Derivatives
title_full Synthesis, Photophysical and Electronic Properties of New Red‐to‐NIR Emitting Donor–Acceptor Pyrene Derivatives
title_fullStr Synthesis, Photophysical and Electronic Properties of New Red‐to‐NIR Emitting Donor–Acceptor Pyrene Derivatives
title_full_unstemmed Synthesis, Photophysical and Electronic Properties of New Red‐to‐NIR Emitting Donor–Acceptor Pyrene Derivatives
title_short Synthesis, Photophysical and Electronic Properties of New Red‐to‐NIR Emitting Donor–Acceptor Pyrene Derivatives
title_sort synthesis, photophysical and electronic properties of new red‐to‐nir emitting donor–acceptor pyrene derivatives
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6973242/
https://www.ncbi.nlm.nih.gov/pubmed/31593316
http://dx.doi.org/10.1002/chem.201904219
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