Issue 65, 2015

The inductive-effect of electron withdrawing trifluoromethyl for thermally activated delayed fluorescence: tunable emission from tetra- to penta-carbazole in solution processed blue OLEDs

Abstract

The non-conjugated inductive effect of trifluoromethyl (CF3) was found to be a new acceptor instead of other conjugated moieties. Two blue emissive compounds, 4CzCF3Ph and 5CzCF3Ph, were synthesized using a simple catalyst-free C–N coupling reaction. Solution-processed TADF devices based on the 5CzCF3Ph dopant exhibit significantly higher efficiency (11.8 cd A−1, 5.2%) than 4CzCF3Ph (1.03 cd A−1, 0.67%) due to the smaller ΔEST value for efficient RISC.

Graphical abstract: The inductive-effect of electron withdrawing trifluoromethyl for thermally activated delayed fluorescence: tunable emission from tetra- to penta-carbazole in solution processed blue OLEDs

Supplementary files

Article information

Article type
Communication
Submitted
21 May 2015
Accepted
01 Jul 2015
First published
02 Jul 2015

Chem. Commun., 2015,51, 13024-13027

Author version available

The inductive-effect of electron withdrawing trifluoromethyl for thermally activated delayed fluorescence: tunable emission from tetra- to penta-carbazole in solution processed blue OLEDs

L. Mei, J. Hu, X. Cao, F. Wang, C. Zheng, Y. Tao, X. Zhang and W. Huang, Chem. Commun., 2015, 51, 13024 DOI: 10.1039/C5CC04126K

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