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Excited-State Lifetime Modulation by Twisted and Tilted Molecular Design in Carbene-Metal-Amide Photoemitters

[Image: see text] Carbene–metal–amides (CMAs) are an emerging class of photoemitters based on a linear donor–linker–acceptor arrangement. They exhibit high flexibility about the carbene–metal and metal–amide bonds, leading to a conformational freedom which has a strong influence on their photophysic...

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Autores principales: Gu, Qinying, Chotard, Florian, Eng, Julien, Reponen, Antti-Pekka M., Vitorica-Yrezabal, Inigo J., Woodward, Adam W., Penfold, Thomas J., Credgington, Dan, Bochmann, Manfred, Romanov, Alexander S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9404540/
https://www.ncbi.nlm.nih.gov/pubmed/36032551
http://dx.doi.org/10.1021/acs.chemmater.2c01938
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author Gu, Qinying
Chotard, Florian
Eng, Julien
Reponen, Antti-Pekka M.
Vitorica-Yrezabal, Inigo J.
Woodward, Adam W.
Penfold, Thomas J.
Credgington, Dan
Bochmann, Manfred
Romanov, Alexander S.
author_facet Gu, Qinying
Chotard, Florian
Eng, Julien
Reponen, Antti-Pekka M.
Vitorica-Yrezabal, Inigo J.
Woodward, Adam W.
Penfold, Thomas J.
Credgington, Dan
Bochmann, Manfred
Romanov, Alexander S.
author_sort Gu, Qinying
collection PubMed
description [Image: see text] Carbene–metal–amides (CMAs) are an emerging class of photoemitters based on a linear donor–linker–acceptor arrangement. They exhibit high flexibility about the carbene–metal and metal–amide bonds, leading to a conformational freedom which has a strong influence on their photophysical properties. Herein we report CMA complexes with (1) nearly coplanar, (2) twisted, (3) tilted, and (4) tilt-twisted orientations between donor and acceptor ligands and illustrate the influence of preferred ground-state conformations on both the luminescence quantum yields and excited-state lifetimes. The performance is found to be optimum for structures with partially twisted and/or tilted conformations, resulting in radiative rates exceeding 1 × 10(6) s(–1). Although the metal atoms make only small contributions to HOMOs and LUMOs, they provide sufficient spin–orbit coupling between the low-lying excited states to reduce the excited-state lifetimes down to 500 ns. At the same time, high photoluminescence quantum yields are maintained for a strongly tilted emitter in a host matrix. Proof-of-concept organic light-emitting diodes (OLEDs) based on these new emitter designs were fabricated, with a maximum external quantum efficiency (EQE) of 19.1% with low device roll-off efficiency. Transient electroluminescence studies indicate that molecular design concepts for new CMA emitters can be successfully translated into the OLED device.
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spelling pubmed-94045402022-08-26 Excited-State Lifetime Modulation by Twisted and Tilted Molecular Design in Carbene-Metal-Amide Photoemitters Gu, Qinying Chotard, Florian Eng, Julien Reponen, Antti-Pekka M. Vitorica-Yrezabal, Inigo J. Woodward, Adam W. Penfold, Thomas J. Credgington, Dan Bochmann, Manfred Romanov, Alexander S. Chem Mater [Image: see text] Carbene–metal–amides (CMAs) are an emerging class of photoemitters based on a linear donor–linker–acceptor arrangement. They exhibit high flexibility about the carbene–metal and metal–amide bonds, leading to a conformational freedom which has a strong influence on their photophysical properties. Herein we report CMA complexes with (1) nearly coplanar, (2) twisted, (3) tilted, and (4) tilt-twisted orientations between donor and acceptor ligands and illustrate the influence of preferred ground-state conformations on both the luminescence quantum yields and excited-state lifetimes. The performance is found to be optimum for structures with partially twisted and/or tilted conformations, resulting in radiative rates exceeding 1 × 10(6) s(–1). Although the metal atoms make only small contributions to HOMOs and LUMOs, they provide sufficient spin–orbit coupling between the low-lying excited states to reduce the excited-state lifetimes down to 500 ns. At the same time, high photoluminescence quantum yields are maintained for a strongly tilted emitter in a host matrix. Proof-of-concept organic light-emitting diodes (OLEDs) based on these new emitter designs were fabricated, with a maximum external quantum efficiency (EQE) of 19.1% with low device roll-off efficiency. Transient electroluminescence studies indicate that molecular design concepts for new CMA emitters can be successfully translated into the OLED device. American Chemical Society 2022-08-04 2022-08-23 /pmc/articles/PMC9404540/ /pubmed/36032551 http://dx.doi.org/10.1021/acs.chemmater.2c01938 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Gu, Qinying
Chotard, Florian
Eng, Julien
Reponen, Antti-Pekka M.
Vitorica-Yrezabal, Inigo J.
Woodward, Adam W.
Penfold, Thomas J.
Credgington, Dan
Bochmann, Manfred
Romanov, Alexander S.
Excited-State Lifetime Modulation by Twisted and Tilted Molecular Design in Carbene-Metal-Amide Photoemitters
title Excited-State Lifetime Modulation by Twisted and Tilted Molecular Design in Carbene-Metal-Amide Photoemitters
title_full Excited-State Lifetime Modulation by Twisted and Tilted Molecular Design in Carbene-Metal-Amide Photoemitters
title_fullStr Excited-State Lifetime Modulation by Twisted and Tilted Molecular Design in Carbene-Metal-Amide Photoemitters
title_full_unstemmed Excited-State Lifetime Modulation by Twisted and Tilted Molecular Design in Carbene-Metal-Amide Photoemitters
title_short Excited-State Lifetime Modulation by Twisted and Tilted Molecular Design in Carbene-Metal-Amide Photoemitters
title_sort excited-state lifetime modulation by twisted and tilted molecular design in carbene-metal-amide photoemitters
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9404540/
https://www.ncbi.nlm.nih.gov/pubmed/36032551
http://dx.doi.org/10.1021/acs.chemmater.2c01938
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