期刊
INORGANICA CHIMICA ACTA
卷 560, 期 -, 页码 -出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.ica.2023.121839
关键词
Asymmetric diphosphine; Pyridyl diphenyl phosphine; Cu(I) halide complex; Thermally activated delayed fluorescence; Structure; Photophysical properties
Thermally activated delayed fluorescent (TADF) Cu(I) halide complexes with short lifetimes and intense emissions were synthesized and characterized. These complexes exhibit intense green to yellow-green delayed fluorescence and are suitable for OLED devices.
Thermally activated delayed fluorescent (TADF) Cu(I) halide complexes have attracted attention due to their highly emission and short lifetimes (several mu s scale). Here, three mononuclear four-coordinate Cu(I) halide complexes containing asymmetric diphosphine and pyridyl phosphine, [CuX(L1)(L2)] (L1 = 2,3-bis(diphenylphoshino)thiophene, L2 = 2-(diphenylphosphino)pyridine, X = I (1), Br(2), Cl (3)), were synthesized and their structures and photophysical properties were characterized. At room temperature, complexes 1-3 in powder exhibit intense green to yellow green delayed fluorescence (lambda(em) = 497-523 nm, tau = 1.5-4.3 mu s, phi = 0.19-0.28). The emissions of the complexes 1-3 are originated from (metal + halide)-to-ligand and intra-ligand charge transfer. More contributions from MLCT and XLCT can result in the shorter decay lifetimes (1.6 similar to 4.3 mu s), which will prevent a roll-off of efficiency with increasing current density in OLED devices.
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