Methacryloyl functionalized hydrazones as hole-transporting materials for electrophotography

• Autorzy: Budreckiene R. , Andruleviciute V. , Buika G. , Grazulevicius J. V. , Jankauskas V. , Grazuleviciene V.
• Języki publikacji: EN

Abstrakty

EN

Syntheses and thermal, optical as well as photoelectrical properties of carbazolyl-, triphenylaminoand 2-hydroxy-4-diethylaminophenyl-based hydrazones with reactive methacryloyl groups have been reported. All the synthesized materials form glasses with glass transition temperatures ranging from 9 to 50 °C. They absorb electromagnetic radiation in the 250-440 nm range. Ionization potentials of the amorphous films of the synthesized materials, established by electron photoemission technique range from 5.20 to 5.71 eV. The lowest ionization potential and the best charge transport properties were observed for 2-(methacryloyl)oxy-4-diethylaminophenyl-1-carbaldehyde N,N-diphenylhydrazone. Time-of-flight hole mobilities in its 50% solid solution in bisphenol Z polycarbonate reach 10-5 cm2/(Vos) at high electric fields.

Słowa kluczowe

EN

reactive hydrazone; glass; ionization potential; charge mobility

• Wydawca: De Gruyter
• Czasopismo: Materials Science Poland
• Rocznik: 2009
• Tom: Vol. 27, No. 1
• Strony: 61--72
• Opis fizyczny: Bibliogr. 17 poz.

Twórcy

autor

Budreckiene R.

autor

Andruleviciute V.

autor

Buika G.

autor

Grazulevicius J. V.

autor

Jankauskas V.

autor

Grazuleviciene V.

• Department of Organic Technology, Kaunas University of Technology, Radvilénu pl. 19, LT-50254 Kaunas, Lithuania

Bibliografia

• [1] STOLKA M., [in:] Special Polymers for Electronics and Optoelectronics, J.A. Chilton, M.T. Goosey (Eds.), Chapman and Hall, London, 1995, p. 284.
• [2] BORSENBERGER P.M., WEISS D.S, Organic Photoreceptors for Xerography, M. Dekker, New York, 1998, p. 768.
• [3] JIANG K.J., SUN Y.L., SHAO K.F, YANG L.M., Chem. Lett., 33 (2004), 50.
• [4] GETAUTIS V., STANISAUSKAITE A., MALINAUSKAS T., STUMBRAITE J., GAIDELIS V., JANKAUSKAS V., Monatsh. Chem., 137 (2006), 1401.
• [5] GETAUTIS V., DASKEVICIENE M., MALINAUSKAS T., GAIDELIS V., JANKAUSKAS V., TOKARSKI Z., Synth. Met., 155 (2005), 599.
• [6] GETAUTIS V., DASKEVICIENE M., MALINAUSKAS T., STANISAUSKAITE A., STUMBRAITE J., Molecules, 11 (2006), 64.
• [7] BUDRECKIENE R., BUIKA G., GRAZULEVICIUS J.V., JANKAUSKAS V., STANISKIENE B., J. Photochem. Photobiol. A. Chem., 181 (2006), 257.
• [8] BUDRECKIENE R., BUIKA G., GRAZULEVICIUS J.V., JANKAUSKAS V., TOKARSKI Z., Synth. Met., 156 (2006), 677.
• [9] LIDLE D.R., Handbook for Organic Solvents, CRC Press, Boca Raton, 1995.
• [10] LEE H.J., SOHN J., HWANG J., PARK S.Y., CHOI H., CHA M., Chem. Mater., 16 (2004), 456.
• [11] OSTRAUSKAITE J., VOSKA V., ANTULIS J., GAIDELIS V., JANKAUSKAS V., GRAZULEVICIUS J.V., J. Mater. Chem., 12 (2002), 3469.
• [12] MIYAMOTO E., YAMAGUCHI Y., YOKOYAMA M., Electrophotography, 28 (1989), 364.
• [13] MONTRIMAS E., GAIDELIS V., PAZERA A., Lithuanian Journal of Physics, 6 (1966), 569.
• [14] VAEZI-NEJAD S.M., Int. J. Electronics, 62, (1987) 361.
• [15] STROHRIEGL P., Mol. Cryst. Liq. Cryst. 183, (1990), 261.
• [16] BUDRECKIENE R., GRAZULEVICIUS J.V., JANKAUSKAS V., VEDEGYTE J., SIDARAVICIUS J., J. Optoelectronics Adv. Mater., 8 (2006), 1533.
• [17] VILSMEIER A., HACK A., Ber. 60 (1927) 119.