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Benzimidazole-Based N,O Boron Complexes as Deep Blue Solid-State Fluorophores

Benzimidazole-based boranils were designed and synthesized in order to assess the influence of halogen substituents on their optoelectronic properties. All compounds are photoluminescent in solution and solid state. Compared to the free ligands, the new boranils emit at a lower wavelength, by elimin...

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Autores principales: Vaz, Patrícia A. A. M., Rocha, João, Silva, Artur M. S., Guieu, Samuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8348718/
https://www.ncbi.nlm.nih.gov/pubmed/34361489
http://dx.doi.org/10.3390/ma14154298
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author Vaz, Patrícia A. A. M.
Rocha, João
Silva, Artur M. S.
Guieu, Samuel
author_facet Vaz, Patrícia A. A. M.
Rocha, João
Silva, Artur M. S.
Guieu, Samuel
author_sort Vaz, Patrícia A. A. M.
collection PubMed
description Benzimidazole-based boranils were designed and synthesized in order to assess the influence of halogen substituents on their optoelectronic properties. All compounds are photoluminescent in solution and solid state. Compared to the free ligands, the new boranils emit at a lower wavelength, by elimination of the excited-state intramolecular proton transfer observed with the ligands. In the solid state, some of the boranils exhibit a deep blue emission, presenting Commission Internationale de l’Éclairage (CIE) coordinates with an x-component of less than 0.16 and a y-component smaller than 0.04, highly desired values for the development of blue emitting materials.
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spelling pubmed-83487182021-08-08 Benzimidazole-Based N,O Boron Complexes as Deep Blue Solid-State Fluorophores Vaz, Patrícia A. A. M. Rocha, João Silva, Artur M. S. Guieu, Samuel Materials (Basel) Article Benzimidazole-based boranils were designed and synthesized in order to assess the influence of halogen substituents on their optoelectronic properties. All compounds are photoluminescent in solution and solid state. Compared to the free ligands, the new boranils emit at a lower wavelength, by elimination of the excited-state intramolecular proton transfer observed with the ligands. In the solid state, some of the boranils exhibit a deep blue emission, presenting Commission Internationale de l’Éclairage (CIE) coordinates with an x-component of less than 0.16 and a y-component smaller than 0.04, highly desired values for the development of blue emitting materials. MDPI 2021-07-31 /pmc/articles/PMC8348718/ /pubmed/34361489 http://dx.doi.org/10.3390/ma14154298 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Vaz, Patrícia A. A. M.
Rocha, João
Silva, Artur M. S.
Guieu, Samuel
Benzimidazole-Based N,O Boron Complexes as Deep Blue Solid-State Fluorophores
title Benzimidazole-Based N,O Boron Complexes as Deep Blue Solid-State Fluorophores
title_full Benzimidazole-Based N,O Boron Complexes as Deep Blue Solid-State Fluorophores
title_fullStr Benzimidazole-Based N,O Boron Complexes as Deep Blue Solid-State Fluorophores
title_full_unstemmed Benzimidazole-Based N,O Boron Complexes as Deep Blue Solid-State Fluorophores
title_short Benzimidazole-Based N,O Boron Complexes as Deep Blue Solid-State Fluorophores
title_sort benzimidazole-based n,o boron complexes as deep blue solid-state fluorophores
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8348718/
https://www.ncbi.nlm.nih.gov/pubmed/34361489
http://dx.doi.org/10.3390/ma14154298
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