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基于多位置包封苯并咪唑铱(III)配合物的小分子玻璃:用于高效溶液处理的无主体电致磷光二极管。

Small molecular glasses based on multiposition encapsulated phenyl benzimidazole iridium(III) complexes: toward efficient solution-processable host-free electrophosphorescent diodes.

机构信息

Key Laboratory of Functional Inorganic Material Chemistry, Ministry of Education and School of Chemistry and Materials, Heilongjiang University, Harbin 150080, People's Republic of China.

出版信息

J Phys Chem B. 2010 Jan 14;114(1):141-50. doi: 10.1021/jp909297d.

Abstract

Three electrophosphorescent small molecular Ir(3+) complexes, Ir(HexPhBI)(3) 1 (HexPhBI = 1-Hexyl-2-phenyl-1H-benzo[d]imidazole), Ir(CzPhBI)(3) 2 (CzPhBI = 9-(6-(2-phenyl-1H-benzo[d]imidazol-1-yl)hexyl)-9H-carbazole), and Ir(Cz(2)PhBI)(3) 3 (Cz(2)PhBI = 9-(6-(4-(1-(6-(9H-carbazol-9-yl)hexyl)-1H-benzo[d]imidazol-2-yl)phenoxy)hexyl)-9H-carbazole), were synthesized in which 3 was designed with the structure of multiposition encapsulation. Compared to the hexyl-substituted 1, 2 and 3 end-capped with the conjugated carbazole moieties have improved thermal stability. X-ray diffraction analysis proved the amorphous state of 2 and 3. High-photoluminescent efficiencies of 3 are achieved as 72% in solution and 61% in solid. It indicates that the peripheral carbazoles not only facilitate the separation of triplet-emission cores and reduce the intermolecular aggregation but also supply a routine for the intermolecular energy transfer. Electrochemical analysis showed the more oxidation states of 3, which might be anticipated to make it superior to 1 and 2 in hole injection and transporting. The important role of the peripheral carbazole moieties in carrier injection/transporting and the optical properties of the complexes were further investigated by Gaussian simulation. A dramatic electroluminescent (EL) performance, including external quantum efficiency of nearly 6%, low turn-on voltage of 2.5 V, and high brightness over 6000 cd m(-2), from the host-free spin-coated device of 3 was achieved. The superiority of multiencapsulation in EL was proved by comparing the EL performance of 2 and 3. By making comparison between the host-free and phosphor-doping devices, it indicated that the combined modification of the aliphatic chains and functional groups in multipositions is a feasible approach to realize the high-efficiency small molecular phosphorescent materials.

摘要

三种电磷光小分子 Ir(3+)配合物,Ir(HexPhBI)(3)1(HexPhBI=1-己基-2-苯基-1H-苯并[d]咪唑),Ir(CzPhBI)(3)2(CzPhBI=9-(6-(2-苯基-1H-苯并[d]咪唑-1-基)己基)-9H-咔唑)和 Ir(Cz(2)PhBI)(3)3(Cz(2)PhBI=9-(6-(4-(1-(6-(9H-咔唑-9-基)己基)-1H-苯并[d]咪唑-2-基)苯氧基)己基)-9H-咔唑),被合成出来,其中 3 的设计结构具有多位置封装。与己基取代的 1 相比,2 和 3 的末端用共轭咔唑基团封端,具有提高的热稳定性。X 射线衍射分析证明了 2 和 3 的非晶态。3 的高荧光效率在溶液中达到 72%,在固体中达到 61%。这表明外围咔唑不仅有利于三重态发射核的分离和减少分子间聚集,而且为分子间能量转移提供了一种常规方法。电化学分析表明 3 具有更多的氧化态,这可能使其在空穴注入和传输方面优于 1 和 2。外围咔唑基团在载流子注入/传输和配合物光学性质中的重要作用通过高斯模拟进一步研究。通过旋涂无主体设备,实现了 3 的戏剧性电致发光(EL)性能,包括近 6%的外量子效率、2.5 V 的低开启电压和超过 6000 cd m(-2)的高亮度。通过比较 2 和 3 的 EL 性能,证明了多封装在 EL 中的优越性。通过比较无主体和磷光掺杂器件,表明在多位置对脂肪链和官能团进行组合修饰是实现高效小分子磷光材料的一种可行方法。

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