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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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