He Ze, Wong Wai-Yeung, Yu Xiaoming, Kwok Hoi-Sing, Lin Zhenyang
Department of Chemistry and Centre for Advanced Luminescence Materials, Hong Kong Baptist University, Waterloo Road, Kowloon Tong, Hong Kong, People's Republic of China.
Inorg Chem. 2006 Dec 25;45(26):10922-37. doi: 10.1021/ic061566c.
The synthesis and structural, photophysical, electrochemical, and electroluminescent properties of a novel class of trifunctional Pt(II) cyclometalated complexes are reported in which the hole-transporting triarylamine, electron-transporting oxadiazole, and electroluminescent metal components are integrated into a single molecule. These neutral metal chelates display good thermal stability (>250 degrees C under N2) and morphological stability. All of them exhibit intense ligand-centered fluorescence and phosphorescence in fluid solutions at room temperature, but the emission spectra become largely dominated by triplet emission bands in CH2Cl2 glass at 77 K. Substituents with different electronic properties were introduced into the bipolar cyclometalating ligands to fine-tune the absorption and emissive characteristics of the compounds, and the results were correlated with theoretical calculations using density functional theory. A comparison of the photophysics and electrochemistry of our multifunctional systems to those only derived from each of the constituent components was also made and discussed. These Pt complexes can be vacuum-sublimed and applied as emissive dopants for the fabrication of vapor-deposited electrophosphorescent organic light-emitting devices (OLEDs), which generally exhibit good device performance with efficiencies up to 3.6%, 11.0 cd A-1, and 5.8 lm W-1. While the electroluminescence energy resembles that recorded in fluid solutions for these Pt emitters, these monochromatic OLEDs can emit tunable colors by varying the aryl ring substituents and the level of doping. Saliently, single dopant white-light electroluminescence, triggered by the simultaneous fluorescence/phosphorescence emission of the metal complexes and a variation of applied driving voltages, has also been realized based on some of these multifunctional complexes with peak electrophosphorescence efficiencies of 6.8 cd A-1 and 2.6%.
报道了一类新型三功能铂(II)环金属化配合物的合成及其结构、光物理、电化学和电致发光性质,其中空穴传输三芳基胺、电子传输恶二唑和电致发光金属组分被整合到单个分子中。这些中性金属螯合物表现出良好的热稳定性(在N2气氛下>250℃)和形态稳定性。它们在室温下的流体溶液中均表现出强烈的以配体为中心的荧光和磷光,但在77K的CH2Cl2玻璃中发射光谱主要由三重态发射带主导。将具有不同电子性质的取代基引入双极环金属化配体中以微调化合物的吸收和发射特性,并将结果与使用密度泛函理论的理论计算相关联。还对我们的多功能体系与仅由各组成成分衍生的体系的光物理和电化学进行了比较和讨论。这些铂配合物可以真空升华,并用作制备气相沉积电磷光有机发光二极管(OLED)的发射掺杂剂,这些器件通常表现出良好的器件性能,效率高达3.6%、11.0 cd A-1和5.8 lm W-1。虽然这些铂发射体的电致发光能量与在流体溶液中记录的相似,但这些单色OLED可以通过改变芳基环取代基和掺杂水平来发射可调颜色。值得注意的是,基于其中一些多功能配合物,还实现了由金属配合物的同时荧光/磷光发射和施加驱动电压的变化引发的单掺杂剂白光电致发光,其峰值电磷光效率为6.8 cd A-1和2.6%。