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首页> 外文期刊>Zeitschrift fur Naturforschung, B. A Journal of Chemical Sciences >Synthesis, photophysical characterization and DFT studies on fluorine-free deep-blue emitting Pt(II) complexes
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Synthesis, photophysical characterization and DFT studies on fluorine-free deep-blue emitting Pt(II) complexes

机译:无氟深蓝色发射Pt(II)配合物的合成,光物理特性和DFT研究

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Herein we show that cyclometalated, square planar Pt(II) complexes can be tuned to achieve deepblue phosphorescent emitters. For this purpose, the introduction of an electron-donating moiety on two different bidentate N boolean AND N and N boolean AND O fluorine-free luminophores, namely 2-(1H-tetrazol-5-yl) pyridine and picolinic acid, was carried out. The remaining two coordination sites of the Pt(II) metal center were filled by a sterically demanding cyclometallating unit, namely a tertiary phosphite C boolean AND P ligand. This ancillary ligand avoids aggregation and provides high solubility in organic solvents. Based on this approach, we were able to blue-shift the emission of the complexes down to 411 nm, and to achieve a maximal photoluminescence quantum yield of 56% in the solid state.
机译:在这里,我们表明,可以调整环金属化的方形平面Pt(II)配合物,以获得深蓝色磷光发射体。为此目的,在两个不同的双齿N boolean AND N和N boolean AND O无氟发光体,即2-(1H-四唑-5-基)吡啶和吡啶甲酸上引入给电子部分。 。 Pt(II)金属中心的其余两个配位位点由空间上要求较高的环金属化单元(即叔亚磷酸酯C布尔AND P配体)填充。这种辅助配体避免了聚集,并在有机溶剂中具有高溶解度。基于这种方法,我们能够将配合物的发射蓝移至411 nm,并在固态下实现56%的最大光致发光量子产率。

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