Modular Nitrogen‐Doped Concave Polycyclic Aromatic Hydrocarbons for High‐Performance Organic Light‐Emitting Diodes with Tunable Emission Mechanisms**

Abstract

Although bowl‐shaped N‐pyrrolic polycyclic aromatic hydrocarbons (PAHs) can achieve excellent electron‐donating ability, their application for optoelectronics is hampered by typically low photoluminescence quantum yields (PLQYs). To address this issue, we report the synthesis and characterization of a series of curved and fully conjugated nitrogen‐doped PAHs. Through structural modifications to the electron‐accepting moiety, we are able to switch the mechanism of luminescence between thermally activated delayed fluorescence (TADF) and room‐temperature phosphorescence (RTP), and to tune the overall PLQY in the range from 9 % to 86 %. As a proof of concept, we constructed solid‐state organic light‐emitting diode (OLED) devices, which has not been explored to date in the context of concave N‐doped systems being TADF/RTP emitters. The best‐performing dye, possessing a peripheral trifluoromethyl group adjacent to the phenazine acceptor, exhibits yellow to orange emission with a maximum external quantum efficiency (EQE) of 12 %, which is the highest EQE in a curved D‐A embedded N‐PAH to date.

Donor–Acceptor Type of Fused-Ring Thermally Activated Delayed Fluorescence Compounds Constructed through an Oxygen-Containing Six-Membered Ring

“…Very recently, Wagner et al reported one of such systems, which realized the maximum external quantum efficiency of 12% for OLED devices. 41 The strategy they adopted for HOMO−LUMO separation is inserting an antiaromatic seven-membered ring between the D and A groups. Further development of rational molecular design strategies is still of the highest priority in the development of D−A-type fused-ring TADF systems.…”

“…As a result, D–A-type fused-ring TADF systems are very rare. Very recently, Wagner et al reported one of such systems, which realized the maximum external quantum efficiency of 12% for OLED devices . The strategy they adopted for HOMO–LUMO separation is inserting an antiaromatic seven-membered ring between the D and A groups.…”

Highly emissive planarizedB,N-diarylated benzonaphthoazaborine compounds for narrowband blue fluorescence

“…1–8 The most widely used strategy is the doping of boron (B) and nitrogen (N) atoms into the PAHs because B and N atoms can exert complementary electron-accepting and electron-donating properties, respectively, on the π-conjugated framework, allowing the modulation of the HOMO and LUMO distributions and their energy gap. 9–18 Among B,N-doped PAHs, the derivatives of B , N -diphenyl-5,10-dihydro-dibenzo-1,4-azaborine, namely, dibenzoazaborine, 19,20 have recently attracted significant attention because the dibenzoazaborine skeleton may constitute the main component of highly efficient emitting materials such as thermally activated delayed fluorescence (TADF) compounds. 21,22 More interestingly, B,N-doped PAHs containing multiple azaborine rings have exhibited excellent photophysical properties such as narrowband emissions with high photoluminescence quantum yields (PLQYs) due to the multi-resonance effects of B and N atoms that confine the HOMO and LUMO on different ring atoms.…”

Comparative study of thermally activated delayed fluorescent properties of donor–acceptor and donor–acceptor–donor architectures based on phenoxazine and dibenzo[a,j]phenazine

“…The singlet–triplet energy splitting between the S 1 and T 1 states (Δ E ST ) and spin–orbit coupling (SOC) play key roles in manifesting the TADF character of an organic compound. To boost the rISC process, ideally, the Δ E ST is zero or even negative [ 12 – 13 ], while the SOC is as large as possible. One of the promising molecular design strategies to meet the above-mentioned criteria involves a highly twisted (D) n –(A) m (D: electron donor; A: electron acceptor) system, in which efficient intramolecular charge transfer (ICT) occurs in the singlet excited state ( 1 CT).…”