A new spin on perovskites untwined: Ultrafast optical switching and tuning of spin-energy states in layered halide perovskites.

A new broadband‐emitting 2 D hybrid organic–inorganic perovskite (CyBMA)PbBr4 based on highly flexible cis‐1,3‐bis(methylaminohydrobromide)cyclohexane (CyBMABr) core has been designed, synthesized, and investigated, highlighting the effects of stereoisomerism of the templating cation on the formation and properties of the resulting perovskite. The new 2 D material has high exciton binding energy of 340 meV and a broad emission spanning from 380 to 750 nm, incorporating a prominent excitonic band and a less intense broad peak at room temperature. Significant changes in the photoluminescence (PL) spectrum were observed at lower temperatures, showing remarkable enhancement in the intensity of the broadband at the cost of excitonic emission. Temperature‐dependent PL mapping indicates the effective role of only a narrow band of excitonic absorption in the generation of the active channel for emission. Based on the evidences obtained from the photophysical investigations, we attributed the evolution of the broad B‐band of (CyBMA)PbBr4 to excitonic self‐trapped states.

Tröger's bases (TBs) functionalized with carbazoles (TB-Czs) and phosphine oxides (TB-POs) were designed and synthesized as host materials for application in phosphorescent organic light-emitting diodes. The TB scaffold is shown to impart thermal stability with high Tg values (171-211 °C) as well as high triplet energies in the range of 2.9-3.0 eV. With a limited experimentation of the devices, it is shown that the TBs doped with a green phosphor, namely, Ir(ppy)3, permit impressive external efficiencies on the order of ca. 16% with a high brightness of ca. 3000-4000 cd/m2. Better device performance results are demonstrated by a small structural manipulation of the TB scaffold involving substitution of methyl groups in the core scaffold.

Dioxiranes are multi-tasking reagents inheriting mild and selective oxygen transfer attributes. These oxidants are accessed from the reaction of ketones with an oxidant and are employed stoichiometrically or catalytically (in...

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