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Effects of Electron Affinity and Steric Hindrance of the Trifluoromethyl Group on the π‐Bridge in Designing Blue Thermally Activated Delayed Fluorescence Emitters
Author(s) -
Li Huiting,
Li Jiuyan,
Liu Di,
Huang Tingting,
Li Deli
Publication year - 2020
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.202000926
Subject(s) - steric effects , trifluoromethyl , bridge (graph theory) , fluorescence , chemistry , photochemistry , stereochemistry , organic chemistry , physics , optics , medicine , alkyl
Abstract To explore the correlation of the acceptor electron affinity and the molecular conformation to the thermally activated delayed fluorescence (TADF) feature, a series of d ‐π‐A molecules were designed and synthesized with triazine (Trz) as the acceptor (A) and carbazole (Cz) or tert ‐butylcarbazole (BuCz) as the donor (D). On the phenylene bridge between D and A, methyl or trifluoromethyl was incorporated close either to D or to A to tune the molecular conformation and the electron‐withdrawing ability of acceptor. Both the twist angles and the singlet and triplet energy difference (Δ E ST ) were observed strongly dependent on the type and position of the substituent on the π‐bridge. Only those molecules with trifluoromethyl locating close to the D side, namely TrzCz‐CF 3 and TrzBuCz‐CF 3 , exhibit TADF feature, verifying that both sufficient electron affinity of the A unit and large dihedral angle between D and the π‐bridge are necessary to ensure the occurrence of TADF. The blue organic light‐emitting diodes fabricated with TrzCz‐CF 3 and TrzBuCz‐CF 3 achieved external quantum efficiencies of 9.40 % and 14.22 % with CIE coordinates of (0.19, 0.23) and (0.18, 0.29) respectively. This study provides practical design strategy for blue TADF materials particularly when planar and less crowded group is used as donor.