Synthesis of 1,3-diphenylethenylcarbazolyl-based charge transporting materials involving electron donating hydrazone moieties and an electron withdrawing 1,3-indandione moiety is reported. The obtained materials were examined by various techniques, including differential scanning calorimetry, UV-Vis spectroscopy, xerographic time of flight technique and the electron photoemission in air method. Photoemission spectra of the amorphous films of the investigated compounds showed ionization potentials of 5.54-5.90 eV. The hole drift mobility was measured by the xerographic time of flight technique. The highest hole drift mobility, exceeding 10-5 cm2/V.s at 6.4 × 105 V/cm electric field, was observed for the 1,3-diphenylethenylcarbazolyl derivative molecularly doped with a N,N-diphenylhydrazone moiety in the polymeric host bisphenol-Z polycarbonate (PC-Z). © 2012 by the authors; licensee MDPI, Basel, Switzerland.
CITATION STYLE
Bubniene, G., Daskeviciene, M., Pukalskas, A., Jankauskas, V., & Getautis, V. (2012). 1,3-Bisdiphenylethenyl-substituted carbazolyl derivatives as charge transporting materials. Molecules, 17(12), 14846–14857. https://doi.org/10.3390/molecules171214846
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