Orwat B, Witkowska E, Kownacki I, Oh M-J, Hoffmann M, Kubicki M, Grzelak I, Marciniec B, Glowacki I, Luszczynska B, Wiosna-Salyga G, Ulanski J, Ledwon P, Lapkowski M
Faculty of Chemistry, Adam Mickiewicz University in Poznan, St. Umultowska 89b, 61-614 Poznan, Poland.
Dalton Trans. 2017 Jul 18;46(28):9210-9226. doi: 10.1039/c7dt01372h.
Iridium C,N-cyclometalated complexes with an ionic structure are considered to be promising candidates for application in host/guest solid-state phosphorescent single-layer devices because the employment of such dopants offers the possibility of reducing their concentration in organic matrices as well as allows obtaining organic light emitting devices (OLEDs) with interesting emission parameters. We report herein a methodology enabling the synthesis of cyclometalated ionic iridium(iii) complexes of the type [Ir(C^N)(N^N)]A according to a three-component one-pot strategy involving the acceleration of the reaction via microwave irradiation. The developed protocol allowed efficient synthesis of a series of new cationic iridium(iii) coordination derivatives, which were isolated and spectroscopically characterized, while the structures of two of them were determined by the X-ray method. Moreover, the iridium(iii) derivatives were subjected to the cyclic voltammetry studies in order to determine the energies of the HOMO and LUMO levels as well as to estimate their electrochemical properties and to predict some electronic properties. Additionally, the ONIOM calculation scheme that was used to predict HOMO-LUMO gaps for the studied Ir(iii) complexes showed a good correlation between the experimental and calculated values. In order to determine the influence of the structure and nature of the ancillary ligand on the location of the maximum emission band, the photophysical properties of the synthesized iridium complexes were characterized. Finally, the selected compounds were used as emitters for the construction of polymer light emitting diodes (PLEDs) based on a poly(N-vinylcarbazole)/2-(4-tert-butylphenyl)-5-(4-biphenyl)-1,3,4-oxadiazole (PVK/PBD) matrix. The highest luminance, above 10 000 cd m, was recorded for the device containing only 1.0 wt% of [Ir(bzq)(1,10-phenanthroline)]PF in the PVK/PBD. The fabricated PLEDs exhibit current efficiency in the range of 1.0 to 2.2 cd A.
具有离子结构的铱C,N-环金属化配合物被认为是有望应用于主/客体固态磷光单层器件的候选材料,因为使用此类掺杂剂有可能降低其在有机基质中的浓度,同时还能获得具有有趣发射参数的有机发光器件(OLED)。我们在此报告一种方法,该方法能够根据三组分一锅法策略合成[Ir(C^N)(N^N)]A类型的环金属化离子铱(III)配合物,其中通过微波辐射加速反应。所开发的方案能够高效合成一系列新的阳离子铱(III)配位衍生物,这些衍生物被分离并通过光谱进行了表征,其中两种衍生物的结构通过X射线方法确定。此外,对铱(III)衍生物进行了循环伏安法研究,以确定最高占据分子轨道(HOMO)和最低未占据分子轨道(LUMO)能级的能量,以及评估它们的电化学性质并预测一些电子性质。此外,用于预测所研究的Ir(III)配合物的HOMO-LUMO能隙的ONIOM计算方案显示,实验值与计算值之间具有良好的相关性。为了确定辅助配体的结构和性质对最大发射带位置的影响,对合成的铱配合物的光物理性质进行了表征。最后,将所选化合物用作基于聚(N-乙烯基咔唑)/2-(4-叔丁基苯基)-5-(4-联苯基)-1,3,4-恶二唑(PVK/PBD)基质构建聚合物发光二极管(PLED)的发光体。对于在PVK/PBD中仅含有1.0 wt% [Ir(bzq)(1,10-菲咯啉)]PF的器件,记录到最高亮度超过10000 cd m。所制备的PLED的电流效率在1.0至2.2 cd A范围内。