Aggregation-induced emission enhancement in charge-transporting derivatives of carbazole and tetra (tri) phenylethylene.
11 November 2017
New tri- or tetraphenylethylene-substituted phenylcarbazole derivatives exhibiting aggregation-induced emission were synthesized by the synthetic route including Pd-catalyzed Suzuki or Buchwald-Hartwig coupling and Heck reactions. The results of evaluation of the thermal, optical, electrochemical, photophysical, and charge-transporting properties of the synthesized derivatives are presented. The compounds possess high thermal stabilities with 5% weight loss temperatures exceeding 350 °C. Some of the synthesized compounds form glasses with glass transition temperature ranging from 77 to 114 °C. Their maximum fluorescence intensity wavelengths are in the range of 472–498 nm.
The highest photoluminescence quantum yield of 43.9% was observed for the solid sample of 2-(4-(4-(1,2,2-triphenylvinyl)phenylethenyl)phenyl)-9-ethylcarbazole. The electron photoemission spectra of the films of the synthesized compounds revealed ionization potentials of 5.49–5.74 eV. Hole drift mobilities in the layers of 9-phenylcarbazole para-substituted with tri- or tetraphenylethylene moities reached 10−3 cm2 V−1 s−1 at moderate electric fields, as established by the time-of-flight technique
Tomkeviciene, A., Sutaite, J., Volyniuk, D., Kostiv, N., Simkus, G., Mimaite, V. and Grazulevicius, J.V., 2017. Aggregation-induced emission enhancement in charge-transporting derivatives of carbazole and tetra (tri) phenylethylene. Dyes and Pigments, 140, pp.363-374.
Redirect to full article: Click Here
Categories: Material & Chemical