Mononuclear copper(i) complexes bearing a 3-phenyl-5-(pyridin-4-yl)-1,2,4-triazole ligand: synthesis, crystal structure, TADF-luminescence, and mechanochromic effects

被引:6
|
作者
Gusev, Alexey [1 ]
Braga, Elena [1 ]
Zamnius, Ekaterina [1 ]
Kiskin, Mikhail [2 ]
Ali, Amjad [3 ]
Baryshnikov, Glib [3 ]
Linert, Wolfgang [4 ]
机构
[1] Crimean Fed Univ, Simferopol 295007, Crimea, Russia
[2] Russian Acad Sci, NS Kurnakov Inst Gen & Inorgan Chem, Moscow, Russia
[3] Linkoping Univ, Dept Sci & Technol, Lab Organ Elect, SE-60174 Norrkoping, Sweden
[4] Vienna Univ Technol, Inst Appl Synthet Chem, Getreidemarkt 9-163-AC, A-1060 Vienna, Austria
基金
俄罗斯科学基金会; 瑞典研究理事会;
关键词
ACTIVATED DELAYED FLUORESCENCE; LIGHT-EMITTING-DIODES; CU(I) COMPLEXES; BLUE; EMISSION; EMITTERS;
D O I
10.1039/d3dt02633g
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Three new mononuclear heteroleptic copper(i) halide complexes, [CuL(PPh3)(2)X] (X = Cl, Br, I), based on 3-phenyl-5-(pyridin-4-yl)-1,2,4-triazole (L) and triphenylphosphine (PPh3) ligands, have been prepared by reaction of CuX (X = Cl, Br, I), L and PPh3 in a molar ratio of 1:1:2 in MeCN solutions. The synthesized complexes exhibit blue light emission in solutions and bright green emission in the crystal state with quantum yields of up to 100%. The luminescence decay analysis and density functional theory calculations revealed that the emission of solid samples at room temperature corresponds to the thermally activated delayed fluorescence, while that at 77 K is assigned to phosphorescence. Utilizing the studied complexes in OLED heterostructures resulted in high-performing green-emitting devices with an external quantum efficiency of up to 13.4%.
引用
收藏
页码:14995 / 15008
页数:14
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