电致发光
化学
取代基
吡啶
有机发光二极管
螯合作用
吡唑
卡宾
金属
量子效率
光化学
结晶学
药物化学
无机化学
材料科学
有机化学
催化作用
图层(电子)
光电子学
作者
Jie Yan,Ze‐Lin Zhu,Chun‐Sing Lee,Shih-Hung Liu,Pi‐Tai Chou,Yun Chi
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2021-10-06
卷期号:26 (19): 6048-6048
被引量:4
标识
DOI:10.3390/molecules26196048
摘要
In this work, we report a series of bis-tridentate Ir(III) metal complexes, comprising a dianionic pyrazole-pyridine-phenyl tridentate chelate and a monoanionic chelate bearing a peripheral carbene and carboline coordination fragment that is linked to the central phenyl group. All these Ir(III) complexes were synthesized with an efficient one-pot and two-step method, and their emission hue was fine-tuned by variation of the substituent at the central coordination entity (i.e., pyridinyl and phenyl group) of each of the tridentate chelates. Their photophysical and electrochemical properties, thermal stabilities and electroluminescence performances are examined and discussed comprehensively. The doped devices based on [Ir(cbF)(phyz1)] (Cb1) and [Ir(cbB)(phyz1)] (Cb4) give a maximum external quantum efficiency (current efficiency) of 16.6% (55.2 cd/A) and 13.9% (43.8 cd/A), respectively. The relatively high electroluminescence efficiencies indicate that bis-tridentate Ir(III) complexes are promising candidates for OLED applications.
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