Journal
JOURNAL OF MOLECULAR STRUCTURE
Volume 1293, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.molstruc.2023.136263
Keywords
Ionic cuprous complexes; Thermally activated delayed fluorescence; Crystal structure; 3-Triazole ligand
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In this study, two novel ionic cuprous complexes were synthesized and their crystal structure, UV absorption, photoluminescent properties, and electrochemical behaviors were investigated. The complexes exhibited outstanding green luminescence in solid state and high photoluminescent quantum yields. The detailed exploration showed that the complexes were typical thermally activated delayed fluorescence materials and they were used as dopants in electroluminescent devices.
Herein two novel ionic cuprous complexes [Cu(POP)(Pytzb)]BF4 (Cu1, POP = bis(2-diphenylphosphinophenyl) ether, Pytzb = 2-(1-(benzyl)-1H-1,2,3-triazol-4-yl)pyridine) and [Cu(Xantphos)(Pytzb)]BF4 (Cu2, Xantphos = 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene) have been synthesized in reasonable yields, and their crystal structure, UV absorption and photoluminescent properties, as well as electrochemical behaviors were investigated. At 300 K, both Cu1 and Cu2 in solid state exhibit outstanding green luminescence peaked at 533 and 526 nm, respectively, with significantly high photoluminescent quantum yields (PLQYs, 47.5 and 60.5%, respectively). Detailed exploration of emission decay times for Cu1 and Cu2 in dependence of temperature demonstrates that the two complexes are typical thermally activated delayed fluorescence (TADF) materials at ambient temperature with TADF proportions of 83 and 80%, respectively. The two complexes were employed as dopants in solution-processed electroluminescent devices.
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