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Since the report of the first high-efficiency, multi-layered, organic light-emitting diode (OLED) [1], much work has been carried out to improve device efficiency and stability. A very successful method for achieving such improvements is by doping a host organic layer with a fluorescent dye of high quantum yield [2,3]. However, the question as to how such dyes are selected and evalu- ated remains. Pyrazoline may be used as this material; pyrazoline derivatives are five-membered, nitrogen-containing heterocyclic compounds which have high hole-transport efficiency, excellent blue emission and high quantum yield [4,5]. Thus, pyrazoline derivatives have been widely used as fluorescent brightening agents, fluorescence chemosensors, hole-transport materials in electro- photography, OLED and as novel fluorescent materials [6e16]. Tri- phenylamine (TPA) and its derivatives has been widely investigated as hole-transporting, photovoltaic materials and electrolumines- cent materials for almost two decades [17e29]. Thus, in this work, it was considered that the incorporation of a triphenylamine fragment within a pyrazoline molecule may increase excelsior efficiency. In this context, six pyrazoline compounds were synthesized (Fig.1) and their structures determined by 1H, 13C NMR and HRMS. Fluorescence emission spectra were red-shifted in CHCl3 from 6 to 7. The solvent |
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yuxingdpy: ½ð±Ò+5, ·ÒëEPI+1 2012-05-07 10:29:40
yuxingdpy: ½ð±Ò+5, ·ÒëEPI+1 2012-05-07 10:29:40
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