Yang Chen, Lai Shiu-Lun, Chan Sharon Lai-Fung, Low Kam-Hung, Cheng Gang, Yeung Kwan-Ting, Kwok Chi-Chung, Che Chi-Ming
HKU-CAS Joint Laboratory on New Materials and Department of Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong, Fax: (+852) 2915-5176; HKU Shenzhen Institute of Research and Innovation, Shenzhen 518053 (China).
Chem Asian J. 2014 Dec;9(12):3572-85. doi: 10.1002/asia.201402782. Epub 2014 Oct 8.
We report the synthesis of a new class of thermally stable and strongly luminescent cyclometalated iridium(III) complexes 1-6, which contain the 2-acetylbenzo[b]thiophene-3-olate (bt) ligand, and their application in organic light-emitting diodes (OLEDs). These heteroleptic iridium(III) complexes with bt as the ancillary ligand have a decomposition temperature that is 10-20 % higher and lower emission self-quenching constants than those of their corresponding complexes with acetylacetonate (acac). The luminescent color of these iridium(III) complexes could be fine-tuned from orange (e.g., 2-phenyl-6-(trifluoromethyl)benzo[d]thiazole (cf3 bta) for 4) to pure red (e.g., lpt (Hlpt=4-methyl-2-(thiophen-2-yl)quinolone) for 6) by varying the cyclometalating ligands (C-deprotonated C^N). In particular, highly efficient OLEDs based on 6 as dopant (emitter) and 1,3-bis(carbazol-9-yl)benzene (mCP) as host that exhibit stable red emission over a wide range of brightness with CIE chromaticity coordinates of (0.67, 0.33) well matched to the National Television System Committee (NTSC) standard have been fabricated along with an external quantum efficiency (EQE) and current efficiency of 9 % and 10 cd A(-1) , respectively. A further 50 % increase in EQE (>13 %) by replacing mCP with bis[4-(6H-indolo[2,3-b]quinoxalin-6-yl)phenyl]diphenylsilane (BIQS) as host for 6 in the red OLED is demonstrated. The performance of OLEDs fabricated with 6 (i.e., [(lpt)2Ir(bt)]) was comparable to that of the analogous iridium(III) complex that bore acac (i.e., [(lpt)2 Ir(acac)]; 6a in this work) [Adv. Mater.- 2011, 23, 2981] fabricated under similar conditions. By using ntt (Hnnt=3-hydroxynaphtho[2,3-b]thiophen-2-yl)(thiophen-2-yl)methanone) ligand, a substituted derivative of bt, the [(cf3bta)2Ir(ntt)] was prepared and found to display deep red emission at around 700 nm with a quantum yield of 12 % in mCP thin film.
我们报道了一类新型的热稳定且强发光的环金属化铱(III)配合物1 - 6的合成,这些配合物含有2 - 乙酰基苯并[b]噻吩 - 3 - 醇盐(bt)配体,并阐述了它们在有机发光二极管(OLEDs)中的应用。这些以bt作为辅助配体的异核铱(III)配合物,相较于其相应的以乙酰丙酮(acac)为配体的配合物,分解温度高10 - 20%,发光自猝灭常数更低。通过改变环金属化配体(C - 去质子化的C^N),这些铱(III)配合物的发光颜色可从橙色(例如,对于4为2 - 苯基 - 6 - (三氟甲基)苯并[d]噻唑(cf3 bta))微调至纯红色(例如,对于6为lpt (Hlpt = 4 - 甲基 - 2 - (噻吩 - 2 - 基)喹诺酮))。特别地,基于6作为掺杂剂(发光体)和1,3 - 双(咔唑 - 9 - 基)苯(mCP)作为主体制备的高效OLEDs,在很宽的亮度范围内呈现稳定的红色发射,其CIE色度坐标为(0.67, 0.33),与美国国家电视系统委员会(NTSC)标准良好匹配,同时外部量子效率(EQE)和电流效率分别为9%和10 cd A⁻¹。通过在红色OLED中用双[4 - (6H - 吲哚并[2,3 - b]喹喔啉 - 6 - 基)苯基]二苯基硅烷(BIQS)替代mCP作为6的主体,证明EQE进一步提高了50% (>13%)。用6(即[(lpt)₂Ir(bt)])制备的OLEDs的性能与在相似条件下制备的带有acac的类似铱(III)配合物(即[(lpt)₂Ir(acac)]; 本工作中的6a) [《先进材料》 - 2011, 23, 2981]相当。通过使用bt的取代衍生物ntt (Hnnt = 3 - 羟基萘并[2,3 - b]噻吩 - 2 - 基)(噻吩 - 2 - 基)甲酮)配体,制备了[(cf3bta)₂Ir(ntt)],发现在mCP薄膜中其在700 nm左右显示深红色发射,量子产率为12%。