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发射性锇(II)配合物与四齿双(吡啶吡唑)螯合物。

Emissive osmium(II) complexes with tetradentate bis(pyridylpyrazolate) chelates.

机构信息

Department of Chemistry, National Tsing Hua University, Hsinchu 30013, Taiwan.

出版信息

Inorg Chem. 2013 May 20;52(10):5867-75. doi: 10.1021/ic302829e. Epub 2013 Apr 26.

Abstract

A tetradentate bis(pyridylpyrazolate) chelate, L, is assembled by connecting two bidentate 3-(trifluoromethyl)-5-(2-pyridyl)pyrazole chelates at the 6 position of the pyridyl fragment with a phenylamido appendage. This chelate was then utilized in the synthesis of three osmium(II) complexes, namely, [Os(L)(CO)2] (4), [Os(L)(PPh2Me)2] (5), and [Os(L)(PPhMe2)2] (6). Single-crystal X-ray structural analyses were executed on 4 and 5 to reveal the bonding arrangement of the L chelate. Phosphine-substituted derivatives 5 and 6 are highly emissive in both solution and the solid state, and their photophysical properties were measured and discussed on the basis of computational approaches. For application, fabrication and analysis of organic light-emitting diodes (OLEDs) were also carried out. The OLEDs using 5 and 6 as dopants exhibit saturated red emission with maximum external quantum efficiencies of 9.8% and 9.4%, respectively, which are higher than that of the device using [Ir(piq)3] as a red-emitting reference sample. Moreover, for documentation, 5 and 6 also achieve a maximum brightness of 19540 cd·m(-2) at 800 mA·cm(-2) (11.6 V) and 12900 cd·m(-2) at 500 mA·cm(-2) (10.5 V), respectively.

摘要

一种四齿双(吡啶吡唑)螯合物 L 通过连接吡啶片段 6 位的两个双齿 3-(三氟甲基)-5-(2-吡啶基)吡唑螯合物和一个苯甲酰胺侧基来组装。该螯合物随后用于合成三种锇(II)配合物,即 [Os(L)(CO)2](4)、[Os(L)(PPh2Me)2](5)和 [Os(L)(PPhMe2)2](6)。对 4 和 5 进行单晶 X 射线结构分析,以揭示 L 螯合物的键合排列。膦取代衍生物 5 和 6 在溶液和固态中都具有高度的发光性,并且根据计算方法测量和讨论了它们的光物理性质。为了应用,还进行了有机发光二极管(OLED)的制造和分析。使用 5 和 6 作为掺杂剂的 OLED 表现出饱和的红色发射,最大外量子效率分别为 9.8%和 9.4%,高于使用 [Ir(piq)3] 作为红色发射参考样品的器件。此外,为了记录,5 和 6 还分别在 800 mA·cm(-2)(11.6 V)时达到 19540 cd·m(-2)的最大亮度,在 500 mA·cm(-2)(10.5 V)时达到 12900 cd·m(-2)的最大亮度。

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