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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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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. |
format | Online Article Text |
id | pubmed-8653344 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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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