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Theoretical study on photophysical properties of a series of functional pyrimidine‐based organic light‐emitting diodes emitters presenting thermally activated delayed fluorescence.

Authors :
Zhu, Qiuling
Guo, Xugeng
Zhang, Jinglai
Source :
Journal of Computational Chemistry. Jun2019, Vol. 40 Issue 16, p1578-1585. 8p.
Publication Year :
2019

Abstract

Issue concerning accurate prediction of the reverse intersystem crossing rate (kRISC) is critical for developing novel efficient thermally activated delayed fluorescence (TADF) materials. In this contribution, the kRISC rates from the lowest excited triplet T1 state to the lowest excited singlet S1 state were evaluated for five donor‐π‐acceptor‐type pyrimidine‐based TADF emitters using the semiclassical Marcus theory. Both the singlet‐triplet energy difference (ΔEST) and spin–orbit coupling (V) between the S1 and T1 states were investigated by performing the density functional theory (DFT) and time‐dependent density functional theory (TD‐DFT) calculations. In addition, their fluorescence emission wavelengths (λem) were also calculated at the TD‐DFT level. The predicted kRISC and λem values are found to reproduce well the available experimental findings. The present results reveal that the kRISC rates of molecules possessing the unsymmetrical diphenyl pyrimidine acceptor core are calculated to be slightly larger than those of their analogues with the symmetrical diphenyl pyrimidine. In addition, introducing two tert‐butyl groups into the 2,7‐positions of the donor moiety of the latter is also an effective method for increasing kRISC when designing TADF emitters. Such a difference is related to the nature of the T1 excited state. A more remarkable charge‐transfer (CT) contribution to the state can achieve a smaller ΔEST, leading to a more efficient RISC process, and consequently a shorter delayed fluorescence lifetime as observed experimentally. © 2019 Wiley Periodicals, Inc. Five molecules exhibiting the TADF behavior were studied theoretically. Calculations reveal that a remarkable charge‐transfer contribution to the T1 excited state can achieve a smaller singlet‐triplet energy difference. This leads to a more efficient reverse intersystem crossing process. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01928651
Volume :
40
Issue :
16
Database :
Academic Search Index
Journal :
Journal of Computational Chemistry
Publication Type :
Academic Journal
Accession number :
135843738
Full Text :
https://doi.org/10.1002/jcc.25808