Photosensitization-Controlled Dynamic Organic Room-Temperature Phosphorescence.

Dynamic organic room temperature phosphorescence (RTP) materials have enabled potential applications in intelligent optoelectronics owing to their reversibly dynamic luminescence features. However, in most reported dynamic RTP materials, chromophores serve dual roles as phosphorescent emitters and oxygen sensitizers. This leads to uncontrollable dynamic processes and a reduction in phosphorescence performance.

Short-range charge transfer for efficient ultra-narrowband deep blue afterglow.

Efficient and narrowband blue organic afterglow materials are critical components for advanced optoelectronic applications, but so far, have been rarely explored. Herein, we report short-range charge transfer-assisted high efficiency and ultra-narrowband deep blue (<450 nm) afterglow from a series of indolocarbazole-based chromophores. The short-range charge transfer within the fused π-conjugated frameworks enlarges the singlet-triplet energy gap and suppresses vibronic coupling and structural relaxations, thus leading to a slow reverse intersystem crossing rate, a long delayed-fluorescence lifetime of up to 186.

Efficient Organic D-π-A Scintillators for Temperature-Adaptive X-Ray Imaging.

Achieving highly efficient organic scintillators for X-ray imaging remains a significant challenge, primarily owing to the inherent difficulty in facilitating rapid radiative decays of both singlet and triplet excitons. To address this limitation, a novel design strategy is introduced that incorporated fluorine atoms to modify the π-bridge of D-π-A molecules, thereby fine-tuning their electronic structures and photophysical properties. The emitters, namely 1FAT and 2FAT, show excellent thermally activated delayed fluorescence (TADF), aggregation-induced delayed fluorescence (AIDF), and room temperature phosphorescence (RTP) excited by ultraviolet light varying with surrounding environments.

High-Efficiency Organic Mechanophosphorescence from A Phenoselenazine Phosphor for Multiple Applications.

Mechanoluminescence (ML) materials with phosphorescent characteristics hold significant potential for applications in pressure sensing and material damage inspection. However, currently reported mechanophosphorescence (MP) materials suffer from low luminescence efficiency and insufficient brightness. Herein, we report a piezoelectric material, -BPM, with an exceptionally high phosphorescence efficiency of 61.

Functional Analysis of in Causing Rice Seedling Blight.

is one of the main pathogens causing rice seedling blight disease. Revealing its pathogenic mechanism is of great significance for formulating prevention and control strategies for rice seedling blight disease. Copper transporting P-type ATPases (Cu-ATPase) is a large class of proteins located on the plasma membrane that utilize the energy provided by ATP hydrolysis phosphorylation to transport substrates across the membrane.

Water-Resistant Organic Room-Temperature Phosphorescence from Block Copolymers.

Room-temperature phosphorescence (RTP) polymers have demonstrated significant potential for various applications due to their unique luminescent properties. However, most conventional RTP polymers are vulnerable to moisture and water, which can disrupt the hydrogen bonding network within the polymer and accelerate the non-radiative decay of triplet excitons of phosphors, leading to the quenching of RTP. Herein, we present a universal strategy to achieve water-resistant RTP polymers by designing amphiphilic block copolymers with microphase-separated structures.

Biology, Pathogenicity, and Genetic Diversity of the Rice Pathogen in Heilongjiang Province, China.

Rice false smut (RFS) is pervasive and has emerged as the primary disease affecting rice productivity. Due to the lack of effective chemical control, disease-resistant varieties are the primary method of managing the disease. This study aimed to investigate the influence of biological characteristics such as hyphal growth rate, spore production and germination ability on the pathogenicity of .

High-Performance Circularly Polarized Phosphorescence by Confining Isolated Chromophores with Chiral Counterions.

Organic room-temperature phosphorescence (RTP) featuring circularly polarized luminescence (CPL) is highly valuable in chiroptoelectronics, but the trade-off issue between luminescence efficiency (Φ) and dissymmetry factor (g) is still challenging to be solved. Here, chiroptical ionic crystals (R/S-DNP) are constructed through ionization-induced assembly, in which isolated chromophore of carboxylic anion is tightly confined by the surrounding chiral counterions. The long-range ordered and chiral counterions with asymmetric stacking are closely connected with isolated chromophores for molecular assembly via high-density electrostatic interactions, thus enabling the simultaneous realization of excellent single-molecule RTP emission and efficient chirality transfer.

Aldehyde Directed In Situ Loading of Ag Nanodots Around the Open Metal Sites of MOFs for the Tandem Catalysis of Nitrate to Ammonia.

Both spatial arrangement and intrinsic activity of electrocatalysts with dual-active sites are widely designed to match the coupling reaction between nitrate and water, in which most of the reactive intermediates can be optimized to achieve a high yield rate of ammonia. Herein, by introducing the aldehyde group inside metal-organic frameworks (MOFs) in advance, an aldehyde-induced method is achieved to direct the in situ nucleation of Ag nanodots depending on the mesopores of MOFs via a simple silver mirror reaction. The key point here is that the spatial arrangement between the aldehyde group and open metal sites is fixed end to end, which makes the aldehyde group a built-in redox-active site to drive the in situ nucleation of Ag nanodots next to the open metal sites of MOFs.

Achieving Efficient X-ray Scintillation of Purely Organic Phosphorescent Materials by Chromophore Confinement.

Scintillators have attracted significant attention due to their wide-ranging applications in both industrial and medical fields. However, one of the ongoing challenges is the efficient utilization of triplet excitons to achieve high radioluminescence efficiency. Here, a series of purely organic phosphors is presented for X-ray scintillation, employing a combined rigid and flexible host-guest doping strategy.

Influenza and the gut microbiota: A hidden therapeutic link.

Background: The extensive community of gut microbiota significantly influences various biological functions throughout the body, making its characterization a focal point in biomedicine research. Over the past few decades, studies have revealed a potential link between specific gut bacteria, their associated metabolic pathways, and influenza. Bacterial metabolites can communicate directly or indirectly with organs beyond the gut via the intestinal barrier, thereby impacting the physiological functions of the host.

The impact of Astragaloside IV on the inflammatory response and gut microbiota in cases of acute lung injury is examined through the utilization of the PI3K/AKT/mTOR pathway.

Objectives: Astragaloside IV (AS-IV) is a natural triterpenoid saponin compound with a variety of pharmacological effects, and several studies have clarified its anti-inflammatory effects, which may make it an effective alternative treatment against inflammation. In the study, we aimed to investigate whether AS-IV could attenuate the inflammatory response to acute lung injury and its mechanisms.

Methods: Different doses of AS-IV (20mg·kg-1, 40mg·kg-1, and 80mg·kg-1) were administered to the ALI rat model, followed by collection of serum and broncho alveolar lavage fluid (BALF) for examination of the inflammatory response, and HE staining of the lung and colon tissues, and interpretation of the potential molecular mechanisms by quantitative real-time PCR (qRT-PCR), Western blotting (WB).

Enabling Visible-Light-Charged Near-Infrared Persistent Luminescence in Organics by Intermolecular Charge Transfer.

Visible light is a universal and user-friendly excitation source; however, its use to generate persistent luminescence (PersL) in materials remains a huge challenge. Herein, the concept of intermolecular charge transfer (xCT) is applied in typical host-guest molecular systems, which allows for a much lower energy requirement for charge separation, thus enabling efficient charging of near-infrared (NIR) PersL in organics by visible light (425-700 nm). Importantly, NIR PersL in organics occurs via the trapping of electrons from charge-transfer aggregates (CTAs) into constructed trap states with trap depths of 0.

Stretchable phosphorescent polymers by multiphase engineering.

Stretchable phosphorescence materials potentially enable applications in diverse advanced fields in wearable electronics. However, achieving room-temperature phosphorescence materials simultaneously featuring long-lived emission and good stretchability is challenging because it is hard to balance the rigidity and flexibility in the same polymer. Here we present a multiphase engineering for obtaining stretchable phosphorescent materials by combining stiffness and softness simultaneously in well-designed block copolymers.

Abnormal thermally-stimulated dynamic organic phosphorescence.

Dynamic luminescence behavior by external stimuli, such as light, thermal field, electricity, mechanical force, etc., endows the materials with great promise in optoelectronic applications. Upon thermal stimulus, the emission is inevitably quenched due to intensive non-radiative transition, especially for phosphorescence at high temperature.

Achieving High-Temperature Phosphorescence by Organic Cocrystal Engineering.

Organic phosphors offer a promising alternative in optoelectronics, but their temperature-sensitive feature has restricted their applications in high-temperature scenarios, and the attainment of high-temperature phosphorescence (HTP) is still challenging. Herein, a series of organic cocrystal phosphors are constructed by supramolecular assembly with an ultralong emission lifetime of up to 2.16 s.

Polymorphism-Dependent Organic Room Temperature Phosphorescent Scintillation for X-Ray Imaging.

Organic phosphorescent scintillating materials have shown great potential for applications in radiography and radiation detection due to their efficient utilization of excitons. However, revealing the relationship between molecule stacking and the phosphorescent radioluminescence of scintillators is still challenging. This study reports on two phenothiazine derivatives with polymorphism-dependent phosphorescence radioluminescence.

Activating Molecular Room-Temperature Phosphorescence by Manipulating Excited-State Energy Levels in Poly(vinyl alcohol) Matrix.

Poly(vinyl alcohol) (PVA) has been found as a wonderful matrix for chromophores to boost their room-temperature phosphorescence (RTP) character by forming abundant hydrogen bonding. Despite the well-utilized protective effect, the constructive role in accelerating the intersystem crossing is less investigated. Here, we focus on its role in manipulating the excited-state energy level to facilitate multiple intersystem crossing channels.

Narrowband Organic Afterglow via Phosphorescence Förster Resonance Energy Transfer for Multifunctional Applications.

Achieving multicolor organic afterglow materials with narrowband emission and high color purity is important in various optoelectronic fields but remains a great challenge. Here, an efficient strategy is presented to obtain narrowband organic afterglow materials via Förster resonance energy transfer from long-lived phosphorescence donors to narrowband fluorescence acceptors in a polyvinyl alcohol matrix. The resulting materials exhibit narrowband emission with a full width at half maximum (FWHM) as small as 23 nm and the longest lifetime of 721.

Thiazol-2-ylidenes as N-Heterocyclic carbene ligands with enhanced electrophilicity for transition metal catalysis.

Over the last 20 years, N-heterocyclic carbenes (NHCs) have emerged as a dominant direction in ligand development in transition metal catalysis. In particular, strong σ-donation in combination with tunable steric environment make NHCs to be among the most common ligands used for C-C and C-heteroatom bond formation. Herein, we report the study on steric and electronic properties of thiazol-2-ylidenes.

Organic phosphorescent scintillation from copolymers by X-ray irradiation.

Scintillators that exhibit X-ray-excited luminescence have great potential in radiation detection, X-ray imaging, radiotherapy, and non-destructive testing. However, most reported scintillators are limited to inorganic or organic crystal materials, which have some obstacles in repeatability and processability. Here we present a facile strategy to achieve the X-ray-excited organic phosphorescent scintillation from amorphous copolymers through the copolymerization of the bromine-substituted chromophores and acrylic acid.

Tetradentate Pt(II) Complexes with Peripheral Hindrances for Highly Efficient Solution-Processed Blue Phosphorescent OLEDs.

Two tetradentate Pt(II) complexes with peripheral bulky-group hindrances [Pt(pzpyOczpy-B1) and Pt(pzpyOczpy-B2)] were synthesized and fully investigated for their structural and blue phosphorescent properties. Both X-ray crystallography and computational simulation revealed that bulky substituents incorporated into the C-pyrazolyl and C-pyridinyl positions lie out of the cyclometallated plane, thus alleviating the intramolecular distortions as well as reducing the intermolecular interaction in the solid state. In dichloromethane, their emission peaks at 460 nm with a narrow full width at half-maximum (FWHM) of less than 50 nm, and the photoluminescent quantum yields are over 95% with short decay lifetimes (<5 μs).

Highly Efficient Blue Phosphorescence from Pillar-Layer MOFs by Ligand Functionalization.

Room temperature phosphorescence (RTP) has been extensively researched in heavy-metal containing complexes and purely organic systems. Despite the rapid blossom of RTP materials, it is still a tremendous challenge to develop highly efficient blue RTP materials with long-lived lifetimes. Taking the metal-organic framework (MOF) as a model, herein, a feasible strategy of ligand functionalization is proposed, including two essential elements, to develop blue phosphorescence materials with high efficiency and long-lived lifetimes simultaneously under ambient conditions.

Purely Organic Room-Temperature Phosphorescence Endowing Fast Intersystem Crossing from Through-Space Spin-Orbit Coupling.

Purely organic room-temperature phosphorescence endowing very fast intersystem crossing from through-space systems has not been well investigated. Here we report three space-confined bridged phosphors, where phenothiazine is linked with dibenzothiophene, dibenzofuran, and carbazole by a 9,9-dimethylxanthene bridge. Nearly pure phosphorescence is observed in the crystals at room temperature.

Circularly Polarized Organic Room Temperature Phosphorescence from Amorphous Copolymers.

Organic optoelectronic functional materials featuring circularly polarized emission and persistent luminescence represent a novel research frontier and show promising applications in data encryption, displays, biological imaging, and so on. Herein, we present a simple and universal approach to achieve circularly polarized organic phosphorescence (CPP) from amorphous copolymers by the incorporation of axial chiral chromophores into polymer chains via radical cross-linked polymerization. Our experimental data reveal that copolymers (/)-PBNA exhibit a maximum CPP efficiency of 30.