Fluorescent oligomers of dibenzothiophene-S,S-dioxide derivatives: the interplay of crystal conformations and photo-physical properties
摘要:
Fluorescent oligomers where the backbone of dibenzothiophene-S,S-dioxide acts as the acceptor and side chains of aryl methoxy, fluorene, and arylamine act as the donors have been effectively synthesized by the palladium-catalyzed Suzuki coupling reactions, and the photo-physical properties of the compounds were investigated. From the single-crystal XRD patterns the compounds reveal a twisted conformation with an intramolecular structure and show close relationship between intramolecular or intermolecular charge transfer and their photo-physical properties. These patterns provide more comprehensive information, which is unattainable from H-1 NMR and 2D-COSY spectra. The emission spectrum in the range of 450-510 nm can be finely tuned by systematically altering the position of substitution on the donor units of side chains connected with the backbone acceptor. The fabricated devices displayed a sky blue to deep green in terms of color and performed the CIE (x,y) coordinates with values of (0.18-0.21, 0.25-0.46), respectively. (c) 2012 Elsevier Ltd. All rights reserved.
Triphenylamine or carbazole-containing dibenzothiophene sulfones: Color-tunable solid-state fluorescence and hypso- or bathochromic mechanofluorochromic behaviors
triphenylamine or carbazole-based highly emissive solid fluorophores (The maximum quantum yield of 42.43%) of dibenzothiophene sulfones have been successfully prepared and characterized. The solid-state emission behaviors and mechanical stimulus-responsive luminescence characteristics of all these donor-acceptor-donor (D-A-D) type or donor-π-acceptor-π-donor (D-π-A-π-D) type compounds 1–4 were investigated
A bipolar triphenylamine-dibenzothiophene <i>S</i>,<i>S</i>-dioxide hybrid compound for solution-processable single-layer green OLEDs and as a host for red emitters
A bipolar triphenylamine-dibenzothiophene S,S-dioxide hybrid compound for solution-processable single-layer green OLEDs and as a host for red emitters.
Dibenzothiophene-S,S-dioxide derivatives containing triphenylamine and tetraphenylethene: Synthesis, aggregation-induced emission and electroluminescence
作者:Aihui Liang、Sifan Hu、Zhiping Wang、Wenjing Zhou、Jiarong Xu、Mingzhong Cai、Dongge Ma
DOI:10.1016/j.dyepig.2020.108526
日期:2020.9
Several well-defined donor-acceptor (D-A) dibenzothiophene-S,S-dioxide (SO) derivatives possessing aggregation-induced emission (AIE) behaviour decorated by tetraphenylethene (TPE) and triphenylamine (TPA) were synthesized and characterized. The photophysical, thermal, electrochemical and electroluminescent (EL) properties, as well as the AIE property of the luminogens were discussed. All the luminogens
合成并表征了几种定义明确的供体-受体(DA)二苯并噻吩-S,S-二氧化物(SO)衍生物,其具有由四苯乙烯(TPE)和三苯胺(TPA)修饰的聚集诱导发射(AIE)行为。讨论了光致发光材料的光物理,热,电化学和电致发光(EL)特性以及AIE特性。所有的发光剂均显示出高的热稳定性,并具有良好的光致发光性,并具有非典型的AIE特性。在这三种OLED中,TPA–FSO–TPA器件表现出最佳性能,其V on为4.0 V,LE最大值为10.05 cd A -1,EQE最大值为3.8%,L最大14,670 cd m -2。随着工作电压的变化,基于TPA–FSO–TPA,TPA–FSO–TPE和TPE–FSO–TPE的器件的电致发光(EL)光谱显示的位移可忽略不计,表明在该系统中可以实现良好的器件稳定性。
MATERIALS FOR ORGANIC ELECTROLUMINESCENT DEVICES
申请人:Bach Ingrid
公开号:US20090167166A1
公开(公告)日:2009-07-02
The present invention relates to compounds according to formula (1) and/or according to formulae (4) to (10) and their use in organic electroluminescent devices, in particular as a matrix material in phosphorescent devices.