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Impact of Donor Substitution Pattern on the TADF Properties in the Carbazolyl-Substituted Triazine Derivatives

Authors :
Paulius Baronas
Karolis Kazlauskas
Juozas V. Grazulevicius
Nadzeya A. Kukhta
Tomas Matulaitis
Dovydas Banevičius
Tadas Buciunas
Paulius Imbrasas
Saulius Jursenas
Source :
The Journal of Physical Chemistry C. 121:23618-23625
Publication Year :
2017
Publisher :
American Chemical Society (ACS), 2017.

Abstract

In this work, we report on the synthesis and photophysical investigation of a new star-shaped triazine-carbazole derivative 2,4,6-tris(3-(3,6-di-tert-butyl-9H-carbazol-9-yl)phenyl)-1,3,5-triazine. Comparative study of the photophysical properties of the newly synthesized emitter along with its para-substituted isomer 2,4,6-tris(4-(3,6-di-tert-butyl-9H-carbazol-9-yl)phenyl)-1,3,5-triazine was performed. While para-linkage caused higher oscillator strength of the lowest energy absorption band and high fluorescence quantum yield, the meta-linkage resulted in stronger charge transfer character as well as higher triplet energy. Delayed emission of meta-isomer was found to be 3 orders of magnitude more intense than that of para-isomer. Temperature dependent measurements of meta-isomer confirmed the thermally activated delayed fluorescence origin of its delayed fluorescence with the activation energy of 0.07 eV. Organic light emitting diode containing this emitter dispersed in bis[2-(diphenylphosphino)phenyl] et...

Details

ISSN :
19327455 and 19327447
Volume :
121
Database :
OpenAIRE
Journal :
The Journal of Physical Chemistry C
Accession number :
edsair.doi...........c63b2062bbd0fef8a3aa290e010cf3a3
Full Text :
https://doi.org/10.1021/acs.jpcc.7b08034