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Brominated B(1)-Polycyclic Aromatic Hydrocarbons for the Synthesis of Deep-Red to Near-Infrared Delayed Fluorescence Emitters
[Image: see text] Bromo-functionalized B(1)-polycyclic aromatic hydrocarbons (PAHs) with LUMOs of less than −3.0 eV were synthesized and used in cross-couplings to form donor–acceptor materials. These materials spanned a range of S(1) energies, with a number showing thermally activated delayed fluor...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10425980/ https://www.ncbi.nlm.nih.gov/pubmed/37498083 http://dx.doi.org/10.1021/acs.orglett.3c02167 |
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author | Yuan, Kang Gupta, Abhishek Kumar Si, Changfeng Uzelac, Marina Zysman-Colman, Eli Ingleson, Michael James |
author_facet | Yuan, Kang Gupta, Abhishek Kumar Si, Changfeng Uzelac, Marina Zysman-Colman, Eli Ingleson, Michael James |
author_sort | Yuan, Kang |
collection | PubMed |
description | [Image: see text] Bromo-functionalized B(1)-polycyclic aromatic hydrocarbons (PAHs) with LUMOs of less than −3.0 eV were synthesized and used in cross-couplings to form donor–acceptor materials. These materials spanned a range of S(1) energies, with a number showing thermally activated delayed fluorescence and significant emission in the near-infrared region of the spectrum. These B(1)-PAHs represent a useful family of acceptors that can be readily synthesized and functionalized. |
format | Online Article Text |
id | pubmed-10425980 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-104259802023-08-16 Brominated B(1)-Polycyclic Aromatic Hydrocarbons for the Synthesis of Deep-Red to Near-Infrared Delayed Fluorescence Emitters Yuan, Kang Gupta, Abhishek Kumar Si, Changfeng Uzelac, Marina Zysman-Colman, Eli Ingleson, Michael James Org Lett [Image: see text] Bromo-functionalized B(1)-polycyclic aromatic hydrocarbons (PAHs) with LUMOs of less than −3.0 eV were synthesized and used in cross-couplings to form donor–acceptor materials. These materials spanned a range of S(1) energies, with a number showing thermally activated delayed fluorescence and significant emission in the near-infrared region of the spectrum. These B(1)-PAHs represent a useful family of acceptors that can be readily synthesized and functionalized. American Chemical Society 2023-07-27 /pmc/articles/PMC10425980/ /pubmed/37498083 http://dx.doi.org/10.1021/acs.orglett.3c02167 Text en © 2023 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 | Yuan, Kang Gupta, Abhishek Kumar Si, Changfeng Uzelac, Marina Zysman-Colman, Eli Ingleson, Michael James Brominated B(1)-Polycyclic Aromatic Hydrocarbons for the Synthesis of Deep-Red to Near-Infrared Delayed Fluorescence Emitters |
title | Brominated B(1)-Polycyclic Aromatic
Hydrocarbons for the Synthesis of Deep-Red to Near-Infrared Delayed
Fluorescence Emitters |
title_full | Brominated B(1)-Polycyclic Aromatic
Hydrocarbons for the Synthesis of Deep-Red to Near-Infrared Delayed
Fluorescence Emitters |
title_fullStr | Brominated B(1)-Polycyclic Aromatic
Hydrocarbons for the Synthesis of Deep-Red to Near-Infrared Delayed
Fluorescence Emitters |
title_full_unstemmed | Brominated B(1)-Polycyclic Aromatic
Hydrocarbons for the Synthesis of Deep-Red to Near-Infrared Delayed
Fluorescence Emitters |
title_short | Brominated B(1)-Polycyclic Aromatic
Hydrocarbons for the Synthesis of Deep-Red to Near-Infrared Delayed
Fluorescence Emitters |
title_sort | brominated b(1)-polycyclic aromatic
hydrocarbons for the synthesis of deep-red to near-infrared delayed
fluorescence emitters |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10425980/ https://www.ncbi.nlm.nih.gov/pubmed/37498083 http://dx.doi.org/10.1021/acs.orglett.3c02167 |
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