首页> 外文期刊>Inorganic Chemistry Communications >Binuclear platinum(II) complexes based on a new bis-bidentate 3,6-di(thien-2-yl)pyridazine skeleton, a novel type of deep-red phosphorescent emitters: Synthesis and nonempirical calculations
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Binuclear platinum(II) complexes based on a new bis-bidentate 3,6-di(thien-2-yl)pyridazine skeleton, a novel type of deep-red phosphorescent emitters: Synthesis and nonempirical calculations

机译:基于新的双头二齿3,6-DI(噻吩-2-基)哒嗪骨架,一种新型深红磷光发射器:合成和非透镜计算

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摘要

Three novel template bis-bidentate ligands based on {3,6-di(thien-2-yl)pyridazine} skeleton and four binuclear Pt(II) complexes containing these metalating templates were synthesized and characterized including photo physical study of two emissive compounds. These complexes display phosphorescence from triplet excited state localized primarily at the thienyl-pyridazine aromatic system, the emission bands being unusually strong shifted (ca. 100 nm/4380 cm(-1)) to the NIR region compared to analogous phenyl-pyridazine complexes. The absorption and emission characteristics of the complexes were analyzed by using DFT and TD DFT calculations. The results of calculations confirm that emission originates from a mixture of (LC)-L-3, (MLCT)-M-3, (LLCT)-L-3 with major contribution of the former excited state and show reasonable agreement with the experimental data.
机译:合成了基于{3,6-DI(噻吩-2-基)吡啶啉}骨架和四个含有金属模板的四个二核Pt(II)配合物的三种新的模板双头二齿配体,并表征了两个发射化合物的照片物理研究。 这些复合物从主要在噻吩基 - 哒嗪芳族系统处局部地位的三重态激发状态散射磷光,与类似苯基 - 哒嗪复合物相比,发射带对NIR区域相比,发射带具有异常强烈的偏移(约100nm / 4380cm(-1))。 通过使用DFT和TD DFT计算分析复合物的吸收和排放特性。 计算结果证实,发射源自(LC)-L-3,(MLCT)-M-3,(LLCT)-L-3的混合物,具有前一种激发态的主要贡献,并与实验表明合理的协议 数据。

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