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

被引:25
作者
Alconchel, Adrian [1 ]
Crespo, Olga [1 ]
Garcia-Orduna, Pilar [1 ]
Concepcion Gimeno, M. [1 ]
机构
[1] Univ Zaragoza CSIC, Dept Quim Inorgan, Inst Sintesis Quim & Catalisis Homogenea ISQCH, E-50009 Zaragoza, Spain
关键词
PHOSPHORESCENT CU(I) COMPLEXES; COPPER(I) COMPLEXES; PHOTOPHYSICAL PROPERTIES; PHENANTHROLINE LIGANDS; EXCITED-STATE; EMISSION; METAL; PERFORMANCE; IMPACT;
D O I
10.1021/acs.inorgchem.1c03092
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Ortho-closo or ortho-nido-carborane-diphosphanes have been selected to prepare the heteroleptic cationic or neutral [Cu(N boolean AND N){(PPh2)(2)C2B10H10}]PF6 (1) and [Cu(N boolean AND N){(PPh2)(2)C2B9H10}] (2) [N boolean AND 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 Delta E(S-1 - T-1), pi(T-1), and pi(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.
引用
收藏
页码:18521 / 18528
页数:8
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