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Closo- or Nido-Carborane Diphosphane as Responsible for Strong Thermochromism or Time Activated Delayed Fluorescence (TADF) in [Cu(N^N)(P^P)](0/+)

[Image: see text] Ortho-closo or ortho-nido-carborane-diphosphanes have been selected to prepare the heteroleptic cationic or neutral [Cu(N^N){(PPh(2))(2)C(2)B(10)H(10)}]PF(6) (1) and [Cu(N^N){(PPh(2))(2)C(2)B(9)H(10)}] (2) [N^N = 2-(4-thiazolyl)benzimidazole], respectively. Complexes 1 and 2 displa...

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Autores principales: Alconchel, Adrián, Crespo, Olga, García-Orduña, Pilar, Gimeno, M. Concepción
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8653344/
https://www.ncbi.nlm.nih.gov/pubmed/34812617
http://dx.doi.org/10.1021/acs.inorgchem.1c03092
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author Alconchel, Adrián
Crespo, Olga
García-Orduña, Pilar
Gimeno, M. Concepción
author_facet Alconchel, Adrián
Crespo, Olga
García-Orduña, Pilar
Gimeno, M. Concepción
author_sort Alconchel, Adrián
collection PubMed
description [Image: see text] Ortho-closo or ortho-nido-carborane-diphosphanes have been selected to prepare the heteroleptic cationic or neutral [Cu(N^N){(PPh(2))(2)C(2)B(10)H(10)}]PF(6) (1) and [Cu(N^N){(PPh(2))(2)C(2)B(9)H(10)}] (2) [N^N = 2-(4-thiazolyl)benzimidazole], respectively. Complexes 1 and 2 display very different emissive behavior. Neutral complex 2 exhibits TADF (time activated delayed fluorescence) which has been studied both as powder and PMMA composite with similar ΔE(S(1) – T(1)), τ(T(1)), and τ(S(1)) in both phases. Cationic complex 1 displays a much lower quantum yield than 2 and does not show TADF, but it exhibits a significant thermochromic luminescence, and its emission is very dependent on the medium. Theoretical studies show that metal–ligand (M–diphosphane) to ligand (L′, diimine) transitions, MLL′CT, are responsible of the transitions which originate the emissive properties, but with very different contribution of the copper center, carborane cluster, and diphosphane phenyl rings for 1 and 2.
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spelling pubmed-86533442021-12-09 Closo- or Nido-Carborane Diphosphane as Responsible for Strong Thermochromism or Time Activated Delayed Fluorescence (TADF) in [Cu(N^N)(P^P)](0/+) Alconchel, Adrián Crespo, Olga García-Orduña, Pilar Gimeno, M. Concepción Inorg Chem [Image: see text] Ortho-closo or ortho-nido-carborane-diphosphanes have been selected to prepare the heteroleptic cationic or neutral [Cu(N^N){(PPh(2))(2)C(2)B(10)H(10)}]PF(6) (1) and [Cu(N^N){(PPh(2))(2)C(2)B(9)H(10)}] (2) [N^N = 2-(4-thiazolyl)benzimidazole], respectively. Complexes 1 and 2 display very different emissive behavior. Neutral complex 2 exhibits TADF (time activated delayed fluorescence) which has been studied both as powder and PMMA composite with similar ΔE(S(1) – T(1)), τ(T(1)), and τ(S(1)) in both phases. Cationic complex 1 displays a much lower quantum yield than 2 and does not show TADF, but it exhibits a significant thermochromic luminescence, and its emission is very dependent on the medium. Theoretical studies show that metal–ligand (M–diphosphane) to ligand (L′, diimine) transitions, MLL′CT, are responsible of the transitions which originate the emissive properties, but with very different contribution of the copper center, carborane cluster, and diphosphane phenyl rings for 1 and 2. American Chemical Society 2021-11-23 2021-12-06 /pmc/articles/PMC8653344/ /pubmed/34812617 http://dx.doi.org/10.1021/acs.inorgchem.1c03092 Text en © 2021 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 Alconchel, Adrián
Crespo, Olga
García-Orduña, Pilar
Gimeno, M. Concepción
Closo- or Nido-Carborane Diphosphane as Responsible for Strong Thermochromism or Time Activated Delayed Fluorescence (TADF) in [Cu(N^N)(P^P)](0/+)
title Closo- or Nido-Carborane Diphosphane as Responsible for Strong Thermochromism or Time Activated Delayed Fluorescence (TADF) in [Cu(N^N)(P^P)](0/+)
title_full Closo- or Nido-Carborane Diphosphane as Responsible for Strong Thermochromism or Time Activated Delayed Fluorescence (TADF) in [Cu(N^N)(P^P)](0/+)
title_fullStr Closo- or Nido-Carborane Diphosphane as Responsible for Strong Thermochromism or Time Activated Delayed Fluorescence (TADF) in [Cu(N^N)(P^P)](0/+)
title_full_unstemmed Closo- or Nido-Carborane Diphosphane as Responsible for Strong Thermochromism or Time Activated Delayed Fluorescence (TADF) in [Cu(N^N)(P^P)](0/+)
title_short Closo- or Nido-Carborane Diphosphane as Responsible for Strong Thermochromism or Time Activated Delayed Fluorescence (TADF) in [Cu(N^N)(P^P)](0/+)
title_sort closo- or nido-carborane diphosphane as responsible for strong thermochromism or time activated delayed fluorescence (tadf) in [cu(n^n)(p^p)](0/+)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8653344/
https://www.ncbi.nlm.nih.gov/pubmed/34812617
http://dx.doi.org/10.1021/acs.inorgchem.1c03092
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