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Strongly phosphorescent platinum(II) complexes supported by tetradentate benzazole-containing ligands

机译:含四齿苯并唑的配体支持的强磷光铂(II)配合物

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A series of strongly phosphorescent Pt(II) complexes (Pt1-Pt3) supported by rigid benzazole-containing tetradentate ligands (L1-L3) were designed and synthesized. The effect of heteroatoms (S, O and N) on the photophysical and electroluminescence properties of Pt(II) complexes was studied systematically. Complex Pt1 based on the benzothiazole-containing ligand exhibited a red-shift in UV-vis and photoluminescence spectra in comparison with Pt2 and Pt3 due to the low electro-negativity and high polarizability of the S atom. Organic light-emitting diodes (OLEDs) with various doping levels of these Pt(II) phosphors were fabricated. At low complex concentration, Pt1, Pt2 and Pt3 mainly showed high energy monomer emission. When the doping ratio was increased, low energy excimer emission was observed for both Pt1 and Pt2. On the contrary, Pt3 dominantly showed monomer emission even at a high doping level because the strong intermolecular interactions were greatly suppressed due to the presence of bulky alkyl chains as revealed by X-ray crystallographic analysis. OLEDs based on these complexes exhibited yellowish green to greenish yellow electro-phosphorescence with high efficiency. Notably, the device based on Pt3 at the doping level of 10 wt% achieved a maximum efficiency of 75.0 cd A(-1), 70.1 lm W-1 and 21.4% with Commission Internationale de L'Eclairage (CIE) coordinates of (0.33, 0.61).
机译:设计并合成了一系列刚性磷光的Pt(II)配合物(Pt1-Pt3),这些配合物由含刚性苯并四唑的四齿配体(L1-L3)支撑。系统地研究了杂原子(S,O和N)对Pt(II)配合物的光物理和电致发光性质的影响。基于P原子的低电负性和高极化率,与Pt2和Pt3相比,基于含苯并噻唑的配体的复合物Pt1在UV-vis和光致发光光谱中显示出红移。制备了具有这些Pt(II)磷光体各种掺杂水平的有机发光二极管(OLED)。在低络合物浓度下,Pt1,Pt2和Pt3主要表现出高能量单体发射。当掺杂比增加时,对于Pt1和Pt2都观察到低能量的准分子发射。相反,Pt3甚至在高掺杂水平下也显示出单体发射,因为X射线晶体学分析表明,由于存在庞大的烷基链,强烈抑制了强烈的分子间相互作用。基于这些配合物的OLED高效地显示出黄绿色至黄绿色的电磷光。值得注意的是,基于Pt3的掺杂水平为10 wt%的器件在国际照明委员会(CIE)坐标为(0.33)的情况下实现了75.0 cd A(-1),70.1 lm W-1和21.4%的最大效率。 ,0.61)。

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