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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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Detalles Bibliográficos
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
Descripción
Sumario:[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.