首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Pyridylpyrazole NN ligands combined with sulfonyl-functionalised cyclometalating ligands for blue-emitting iridium(III) complexes and solution-processable PhOLEDs
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Pyridylpyrazole NN ligands combined with sulfonyl-functionalised cyclometalating ligands for blue-emitting iridium(III) complexes and solution-processable PhOLEDs

机译:吡啶基吡唑NN配体与磺酰基官能化的环荷酸配体相结合,用于蓝色发射铱(III)配合物和溶液加工的Pholeds

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摘要

A series of blue iridium(III) complexes (12-15) comprising sulfonyl-functionalised phenylpyridyl cyclometalating ligands and pyridylpyrazole N<^>N ligands are reported, with an X-ray crystal structure obtained for 12. The complexes are highly emissive with photoluminescence quantum yields of 0.52-0.70 in dichloromethane solutions: two of the complexes (12 and 14) show emissions at lambda(PL)(max) 457 nm which is considerably blue-shifted compared to the archetypal blue emitter FIrpic (lambda(max) 468 nm). The short excited state lifetimes (1.8-3.3 mu s) and spectral profiles are consistent with phosphorescence from a mixture of ligand-centred and MLCT excited states. Density functional (DFT) and time dependent DFT (TD-DFT) calculations are in agreement with the electrochemical properties and the blue phosphorescence of the complexes. The additional mesityl substituent on the pyridylpyrazole ligand of 12 and 13 enhances the solubility of the complexes facilitating thin film formation by solution processing. Phosphorescent organic light-emitting diodes (PhOLEDs) have been fabricated using 12 or 13 in a solution-processed single-emitting layer using either poly(vinylcarbazole) (PVK) or 1,3-bis(N-carbazolyl) benzene (mCP) as host. The most blue-shifted electroluminescence (lambda(EL)(max) 460 nm, CIEx,y 0.15, 0.21) is obtained for an OLED containing complex 12 and mCP, with a brightness of 5400 cd m(-2) at 10 V which is high for PhOLEDs with similar blue CIE coordinates using a solution-processed emitter layer.
机译:报道了一系列蓝色铱(III)复合物(12-15),其包含磺酰基官能化苯基吡啶基环偶乙烯基吡啶和吡啶基吡唑N <^> N型配体,得到X射线晶体结构12.复合物具有光致发光的高发光二氯甲烷溶液中的量子产率为0.52-0.70:两种配合物(12和14)显示出λ(PL)(MAX)457nm的排放,与原型蓝色发射器FIRPIC相比,其相比之下是蓝色移位(Lambda(MAX)468 nm)。短兴奋状态寿命(1.8-3.3μs)和光谱谱与来自亚麻定为和MLCT激发态的混合物的磷光一致。密度函数(DFT)和时间依赖性DFT(TD-DFT)计算与电化学性质和复合物的蓝色磷光相一致。吡啶基吡唑配体上的另外的乙基吡唑配体取代基增强了通过溶液加工促进薄膜形成的复合物的溶解度。使用聚(乙烯基咔唑)(PVK)或1,3-双(N-咔唑基)苯(MCP),在溶液加工的单发光层中使用12或13制造磷光有机发光二极管(Pholeds)。主持人。对于含有络合物12和MCP的OLED,获得最大蓝移电致发光(Lambda(EL)(MAX)460nm,Ciex,Y 0.15,0.21),其亮度为5400cdm(-2),在10 v使用溶液处理的发射极层具有类似的蓝色CIE坐标的Pholed高。

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