Recent advances on organic blue thermally activated delayed fluorescence (TADF) emitters for organic light-emitting diodes (OLEDs)

• Thanh-Tuân Bui,
• Fabrice Goubard,
• Malika Ibrahim-Ouali,
• Didier Gigmes and
• Frédéric Dumur

Beilstein J. Org. Chem. 2018, 14, 282–308, doi:10.3762/bjoc.14.18

• activity of the scientific community in this field. Recently, a great deal of interest has been devoted to the elaboration of emitters exhibiting a thermally activated delayed fluorescence (TADF). By a specific molecular design consisting into a minimal overlap between the highest occupied molecular

• emission [9]. This new family of light emitting materials capable to compete with the well-established triplet emitters and displaying a similar efficiency in devices by developing a new emission mechanism was immediately termed as the third generation of OLEDs emitters that consists of thermally activated

• delayed fluorescence (TADF) emitters. As specificity, these materials can thermally repopulate the singlet state from the triplet state by reverse intersystem crossing (RISC), leading to an increase of the luminescence intensity. From the OLEDs viewpoint, TADF emitters behave by harvesting both singlet

Palladium-catalyzed synthesis of N-arylated carbazoles using anilines and cyclic diaryliodonium salts

• Stefan Riedmüller and
• Boris J. Nachtsheim

Beilstein J. Org. Chem. 2013, 9, 1202–1209, doi:10.3762/bjoc.9.136

• , or as host or luminescent-materials in electronic devices (OLEDs) (Figure 1) [2][3][4][5][6][7]. Representative examples are the host molecules mCP, CBP and CBZ1-F2, the hole transporter BCz2 [8] or the recently described thermally activated delayed fluorescence (TADF) emitter 4CzIPN [9]. Therefore