149676-16-4Relevant articles and documents
Glass-forming hole-transporting triphenylamine-based hydrazones with reactive functional groups
Matoliukstyte, Ausra,Grazulevicius, Juozas Vidas,Jankauskas, Vygintas
, p. 85 - 100 (2007)
Synthesis and the properties of a series of triphenylamine-based hydrazones are reported. The dependence of their thermal and glass-forming properties on their chemical structure is discussed. The ionization potentials of the synthesized hydrazones measured by the electron photoemission technique range from 5.16 to 5.32 eV. Hole-drift mobilities of some derivatives molecularly dispersed in bisphenol Z polycarbonate exceed 10-4cm2V-1s-1 at high electric fields (106V/cm),at room temperature.
Triphenylamine derivative, charge-transporting material comprising the same, and electrophotographic photoreceptor
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, (2008/06/13)
A triphenylamine derivative, represented by the following general formula (1): STR1 wherein R1, R2, R3, R4, R5 and R6 each represents a hydrogen atom, a lower alkyl group, an alkoxy group, a halogen atom or an aryl group which may have a substituent group; and m and n each represents 0 or 1.
