Nickel/Photoredox-Catalyzed Asymmetric Three-Component Cross-Coupling To Access Enantioenriched 1,1-Diaryl(heteroaryl)alkanes.

An enantioselective 1,2-dicarbofunctionalization of vinyl (hetero)arenes with alkyl bromides and aryl bromides through nickel/photoredox catalysis is described. This three-component enantioselective domino alkyl arylation of vinyl (hetero)arenes could generate a diverse array of enantioenriched 1,1-diaryl(heteroaryl)alkanes with good to excellent yields (up to 88%) and high enantioselectivities (up to 99% ). This transformation could proceed well under mild conditions with excellent chemo- and regioselectivity due to the avoidance of the use of air- and moisture-sensitive organometallic reagents and stoichiometric metal reductants.

Laser-induced graphene/gold nanoparticle hybrid sensor for enhanced electrochemical detection of paracetamol.

This research presents a highly sensitive and selective electrochemical sensor for detecting paracetamol. The sensor is created using laser direct-writing on a flexible PI substrate to form LIG electrodes. Gold nanoparticles (AuNPs) are then synthesized on the working electrode through secondary laser reduction, resulting in an AuNPs/LIG composite.

Construction of dual-signal output sensing platform for different scene of rapid and sensitive ochratoxin A detection in corn.

Photoelectrochemical (PEC) is a highly sensitive and fast analytical method that can be used at low concentrations, while photoelectrochromic is a simple and low-cost method primarily utilized for high concentration detection. Therefore, we have developed a dual-signal output sensing platform based on both PEC and photoelectrochromism for rapid and sensitive OTA detection. The sensing platform is divided into signal generation (SG) region and signal output (SO) region, which modified with WO/BiVO photoactive nanocomposites and polyaniline (PANI), respectively.

An explore method for quick screening biomarkers based on effective enrichment capacity and data mining.

Protein glycosylation acts as a crucial role in regulating protein function and maintaining cellular homeostasis. Efficient peptide enrichment can be utilized to effectively solve the inherent challenges of protein glycosylation analysis to search unknown cancer biomarkers. In this research, a low dimensional porous hydrophilic nanosheets with a multi-level porous structure (Co-MOF-SiO@HA) was synthetized via an easy one-pot method for the efficient enrichment of the N-glycopeptides in the digests of complex biosamples.

The Degradation and Migration of Cyclanilide in Soil and Sediment in China.

The environmental fate of a plant growth regulator cyclanilide was studied in this paper. The degradation, adsorption, and migration behaviors of cyclanilide were detailly measured in the laboratory. The results showed that the DT of cyclanilide degradation in the Jiangxi red, Taihu paddy, Changshu wushan, Shaanxi tide, and Dongbei black soils was 42.

A Review on Recent Trends in Photo-Drug Efficiency of Advanced Biomaterials in Photodynamic Therapy of Cancer.

Photodynamic Therapy (PDT) has emerged as a highly efficient and non-invasive cancer treatment, which is crucial considering the significant global mortality rates associated with cancer. The effectiveness of PDT primarily relies on the quality of the photosensitizers employed. When exposed to appropriate light irradiation, these photosensitizers absorb energy and transition to an excited state, eventually transferring energy to nearby molecules and generating Reactive Oxygen Species (ROS), including singlet oxygen [1O2].

Perylene-Embedded Helical Nanographenes with Emission up to 1010 nm: Synthesis, Structures, and Chiroptical Properties.

Near-infrared (NIR) circularly polarized absorbing or emitting materials offer distinct advantages over their visible-light counterparts and have attracted considerable interest across various fields. Materials exhibiting NIR chiroptical properties with high fluorescence quantum yields (Φ) are particularly rare. In this study, we report the synthesis of a series of helical nanographenes (1, 2, 3, and 4), where perylene is fused with one to four hexa-peri-hexabenzocoronene (sub) units by a strategy involving Diels-Alder cycloaddition followed by a Scholl reaction.

Upgrading of nitrate to hydrazine through cascading electrocatalytic ammonia production with controllable N-N coupling.

Nitrogen oxides (NO) play important roles in the nitrogen cycle system and serve as renewable nitrogen sources for the synthesis of value-added chemicals driven by clean electricity. However, it is challenging to achieve selective conversion of NO to multi-nitrogen products (e.g.

Development and experimental validation of computational methods for human antibody affinity enhancement.

High affinity is crucial for the efficacy and specificity of antibody. Due to involving high-throughput screens, biological experiments for antibody affinity maturation are time-consuming and have a low success rate. Precise computational-assisted antibody design promises to accelerate this process, but there is still a lack of effective computational methods capable of pinpointing beneficial mutations within the complementarity-determining region (CDR) of antibodies.

Exploring the Impact of In Situ-Formed Solid-Electrolyte Interphase on the Cycling Performance of Aluminum Metal Anodes.

Unwanted processes in metal anode batteries, e.g., non-uniform metal electrodeposition, electrolyte decomposition, and/or short-circuiting, are not fully captured by the electrolyte bulk solvation structure but rather defined by the electrode-electrolyte interface and its changes induced by cycling conditions.

Bio-based hydrogels induced by salts.

In this study, we introduce a salt-responsive hydrogel system utilizing a sugar-derived surfactant featuring a polyhydroxy spacer in its headgroup. The inclusion of salts enhances and organizes the intermolecular hydrogen bonding within the hydrophilic region of the polyhydroxy spacer, promoting cross-linking among surfactant molecules.

Palladium-Catalyzed Cross-Electrophile Couplings of Aryl Thianthrenium Salts with Aryl Bromides via C-S Bond Activation.

We report here a step-economic and cost-effective cross-electrophile coupling of aryl thianthrenium salts with widely available aryl bromides, which proceeded effectively via C-S bond activation at ambient temperature in THF in the presence of a palladium catalyst, magnesium turnings, and lithium chloride to enable the facile assembly of a wide array of structurally diverse biaryls in modest to good yields with good functional group compatibility. In addition, the gram-scale reaction could also be realized.

Proteomic and metabolomic analysis of plasma for pain at different labor stages.

Labor pain has an important impact on maternal labor experience, mood, and postpartum depression. It is of great emotional significance to pay attention to the pain stress response of pregnant women and take necessary intervention measures in the labor process to weaken the sense of delivery experience and reduce the risk of complications. To better understand the molecular alteration of pain and stress changes during the delivery, we analyzed the metabolomic and proteomic of the plasma collected during the labor process at different stages, revealing the significant changes in metabolites and proteins and the key regulatory pathways.

Protocol for hydroxylating aryl chlorides catalyzed by photouranium with water under ambient conditions.

Here, we present a protocol for the hydroxylation of aryl chlorides catalyzed by photouranium with water under ambient conditions. We describe steps for gram-scale hydroxylation of 2'-chloroacetophenone using our self-designed continuous-flow photoreactor. We then detail procedures for obtaining 2'-hydroxyacetophenone using our self-designed rapid separation and purification instrument.

Catalyst-Free [4+1] Annulation of α-Imidoyl Sulfoxonium Ylides and Diazo Compounds Enabling the Modular Synthesis of 2-Indanones and 3(2)-Furanones.

A novel substrate-regulated [4+1] annulation of α-imidoyl sulfoxonium ylides with diazoketones under catalyst-free conditions is described. The reaction proceeds through a coupling of sulfoxonium ylides and in situ-generated ketenes to form the key reactive zwitterionic intermediates, followed by selective formation of C-C or C-O bonds to achieve five-membered ring systems. The cascade reaction permits the direct synthesis of synthetically useful 2-indanones and 3(2)-furanones, which expands the reaction pattern of sulfoxonium ylides in annulation transformation.

Interfacial Anion-Induced Dispersion of Active Species for Efficient Electrochemical Baeyer-Villiger Oxidation.

Degradable polymers are an effective solution for white plastic pollution. Polycaprolactone is a type of degradable plastic with desirable mechanical and biocompatible properties, and its monomer, ε-caprolactone (ε-CL), is often synthesized by Baeyer-Villiger (B-V) oxidation that demands peroxyacids with low safety and low atom-efficiency. Herein, we devised an electrochemical B-V oxidation system simply driven by HO for the efficient production of ε-CL.

Achieving Tunable Monomeric TADF and Aggregated RTP via Molecular Stacking.

Organic emitters with both thermally activated delayed fluorescence (TADF) and room-temperature phosphorescence (RTP) have attracted widespread interest for their intriguing luminescent properties. Herein, a series of triphenylamine-substituted isoquinoline derivatives possessing monomeric TADF and aggregated RTP properties are reported. As the molecules exhibited various forms of π-π and charge transfer (CT) stacking with different intensities, inter/intramolecular CT can be meticulously modulated to achieve tunable TADF-RTP.

Mechanistic insights into NH-assisted selective reduction of NO on CeO: a first-principles microkinetic study on selectivity and activity.

To understand the activity- and selectivity-limiting factors of selective catalytic reduction of NO with NH (NH-SCR) catalyzed by CeO-based oxides, a molecular-level mechanistic exploration was performed on CeO(110) using a first-principles microkinetic study. Herein, the favored reaction pathway for N formation on CeO(110) is unveiled, which includes three key subprocesses. (i) NH adsorbs on the Ce site and dissociates into *NH assisted by O; (ii) *NH preferentially couples with NO adsorbed on O (ONO#), forming *NHNO on the Ce site; (iii) *NHNO undergoes dehydrogenation into *NHNO, which can be easily anchored by O and can then decompose into N.