Simultaneous enhancement of out-coupling efficiency, internal quantum efficiency, and color purity in thermally activated delayed fluorescence (TADF) emitters is highly desired for the practical application of these materials. We designed and synthesized two isomeric TADF emitters, 2DPyM-mDTC and 3DPyM-pDTC, based on di(pyridinyl)methanone (DPyM) cores as the new electron-accepting units and di(tert-butyl)carbazole (DTC) as the electron-donating units. 3DPyM-pDTC, which is structurally nearly planar with a very small ΔE, shows higher color purity, horizontal ratio, and quantum yield than 2DPyM-mDTC, which has a more flexible structure. An electroluminescence device based on 3DPyM-pDTC as the dopant emitter can reach an extremely high external quantum efficiency of 31.9% with a pure blue emission. This work also demonstrates a way to design materials with a high portion of horizontal molecular orientation to realize a highly efficient pure-blue device based on TADF emitters.
A new cobalt-catalyzed coupling of aryl halides with thiophenols and alkanethiols is reported. A variety of aryl sulfides can be prepared in excellent yields under mild reaction conditions using 1-2 mol % of CoI2(dppe) and Zn. This new cobalt-catalyzed coupling represents an interesting addition to previously known methods to synthesize thioethers. [reaction: see text].
Efficient thermally activated delayed fluorescence was observed from a spiro-anthracenone derivative (ACRSA). An organic light-emitting diode containing ACRSA exhibited blue-greenish electroluminescence with a maximum external quantum efficiency of 16.5%.
An idealized bipolar host material and dopant are synthesized for deep‐red phosphorescent organic light‐emitting diodes (PhOLEDs). The host material exhibits a low‐lying lowest unoccupied molecular orbital and high thermal and morphological stability, while the dopant emits sharply at 616 nm with a full width at half‐maximum of only 39 nm. The new host/guest combination for the deep‐red device yields the highest device efficiencies to date.
We investigated the relaxation dynamics of bis(2-phenylpyridinato-)(2,2'-bipyridine)iridium(III), [Ir(ppy)(2)bpy](+) using the technique of time-resolved spectroscopy. In the visible emission spectra this molecule exhibits triple phosphorescence: displaying blue, green, and orange bands. From the dependence of spectral shifts with polarity of solvent, decay lifetimes, and the results of calculations using time-dependent density functional theory, we assigned these three emitting states to be triplet interligand charge-transfer ((3)LLCT), metal-to-ligand ppy charge transfer ((3)MLCT(ppy)), and metal-to-ligand bpy charge transfer ((3)MLCT(bpy)) states. The blue states were formed promptly after excitation at wavelength 355 nm; the one lying at higher energy decaying with a time coefficient 0.79-2.56 ns is assigned to be a triplet MLCT, and the other at lower energy decaying in 1.5-2.8 μs is assigned to (3)LLCT(A), A symmetry. This decay time coefficient of (3)LLCT(A) decreases with increasing dielectric constant of the solvent indicating this state mixing of some MLCT character. The green state (3)MLCT(ppy) decays in 0.13-4.8 ns to a nearby intermediate state either (3)MLCT(ppy) or (3)MLCT(bpy). The orange state (3)MLCT(bpy) is coupled to the intermediate state to have a rise time about 0.36-0.84 ns and decays in 425-617 ns. Although many triplet states exist in a small energy range, they couple weakly to display triple emission. All (3)LLCT and (3)MCLT states are coupled to the singlet (1)LLCT manifold directly and/or indirectly and contribute to the emission in the visible range.
Many steps make light work: substituted phenanthridinones can be obtained with high regioselectivity and in very good yields by palladium-catalyzed cyclization reactions of N-methoxybenzamides with arenes. The reaction proceeds through multiple oxidative C-H activation and C-C/C-N formation steps in one pot at room temperature, and thus provides a simple method for generating bioactive phenanthridinones.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.