Isolation and characterization of a triplet nitrene.

Nitrene radical compounds are short-lived intermediates in a variety of nitrogen-involved transformations. They feature either a singlet or a triplet ground state, depending on the electronic properties of the substituents. Triplet nitrenes are highly reactive and their isolation in the condensed phase under ambient conditions is challenging.

Truncating the C terminus of formate dehydrogenase leads to improved preference to nicotinamide cytosine dinucleotide.

Formate dehydrogenase (FDH) is widely applied in regeneration of redox cofactors. There are continuing interests to engineer FDH for improved catalytic activity and cofactor preference. In the crystal structure of FDH from Pseudomonas sp.

How Carbene Ligands Transform AuAg Alloy Nanoclusters for Electrocatalytic Urea Synthesis.

Metal nanoclusters stabilized by N-heterocyclic carbene (NHC) ligands have attracted increasing interest for their special structures and diverse applications. However, developing synthetic strategies and extending the database of NHC-protected nanoclusters are still challenging tasks. In this work, a novel and rapid synthetic method is developed to prepare AuAg alloy nanocluster ligated by carbene based on the reactivity of nanoclusters.

6-Trifluoromethylnicotinamide Bilaterally Anchored All Cations Implementing Efficient and Humidity-Stable Perovskite Solar Cells.

For organic-inorganic hybrid perovskite solar cells (PSCs), the volatilization of organic components and the presence of undercoordinated Pb ions are the primary causes of device stability imbalance. These factors also serve as significant determinants that restrict the commercialization scale of PSCs. Here, 6-trifluoromethylnicotinamide (TNA) molecules, featuring amide and trifluoromethyl groups at both ends, were introduced as Lewis additives into the precursor solution of perovskite to anchor all cation defect sites and optimize the crystallization process of perovskite.

Experimental Spin-Orbit State-Resolved Differential Cross Sections of the S(D) + D → SD(Π) + D Reaction at Collision Energies of 266.2 and 206.5 cm.

The S(D) + D → SD + D reaction is a prototype insertion chemical reaction that involves spin-orbit interactions in the exit channel. In this work, we report spin-orbit state-resolved differential cross sections (DCSs) of this reaction obtained by crossed beam experiments at collision energies of 266.2 and 206.

Dual activation of soybean resistance against Phytophthora sojae by pectin lyase and degraded pectin oligosaccharides.

Phytophthora pathogens secrete numerous apoplastic effectors to manipulate host immunity. Herein, we identified a polysaccharide lyase 1 protein, PsPL1, which acts as an essential virulence factor of P. sojae infection in soybean.

Dynamic Self-Healing of the Reconstructed Phase in Perovskite Oxides for Efficient and Stable Electrocatalytic OER.

Neither electrocatalytic activity nor structural stability is inconsequential in water electrolysis. Unfortunately, they have to be compromised in practice, especially in the anodic redox chemistry of lattice oxygen. Herein, the discovery of a La CeFeO perovskite is presented which shows both good stability and high catalytic activity.

Photodissociation dynamics of H2S+ via the A2A1 (0, 8, 0) state.

The photodissociation dynamics of the hydrogen sulfide cation (H2S+) (X2B1) were investigated using the time-sliced velocity map ion imaging technique. S+ (4Su) product images were measured at four photolysis wavelengths around 393.70 nm, corresponding to the excitation of the H2S+ (X2B1) cation to the A2A1 (0, 8, 0) state.

Diagnosis and prognosis prediction of gastric cancer by high-performance serum lipidome fingerprints.

Early detection is warranted to improve prognosis of gastric cancer (GC) but remains challenging. Liquid biopsy combined with machine learning will provide new insights into diagnostic strategies of GC. Lipid metabolism reprogramming plays a crucial role in the initiation and development of tumors.

Stereoselective Radical Acylfluoroalkylation of Bicyclobutanes via N-Heterocyclic Carbene Catalysis.

Cyclobutanes are prominent structural components in natural products and drug molecules. With the advent of strain-release-driven synthesis, ring-opening reactions of bicyclo[1.1.

Co-infiltration and dynamic formation of PdZnC intermetallic carbide by syngas boosting selective hydrogenation of acetylene.

Transition metal carbide shows excellent performance in selective hydrogenation of acetylene, however, the carburization of Pd-based intermetallic compounds remains infeasible. Here we report the successful synthesis of an unprecedented PdZnC intermetallic carbide, via co-infiltration of zinc and carbon in one-step carburization by syngas. Utilizing state-of-the-art in situ characterizations and theoretical calculation, we unveil the dynamic evolution of PdZnC during carburization, forming a PdZn like cubic phase carbide structure.

Spontaneously Blinkogenic Probe for Wash-Free Single-Molecule Localization-Based Super-Resolution Imaging in Living Cells.

Single-molecule localization super-resolution fluorescence imaging relies on the fluorescence ON/OFF switching of fluorescent probes to break the diffraction limit. However, the unreacted or nonspecifically bound probes cause non-targeted ON/OFF switching, resulting in substantial fluorescence background that significantly reduces localization precision and accuracy. Here, we report a blinkogenic probe HM-DS655-Halo that remains blinking OFF until it binds to HaloTag, thereby triggering its self-blinking activity and enabling its application in direct SMLM imaging in living cells without wash-out steps.

2D Nano-Photosensitizer Facilitates Proximity Labeling for Living Cells Surfaceome Deciphering.

Photocatalytic proximity labeling has shown great promise for mapping the spatiotemporal dynamics of surfaceome. Although cell-surface targeting photosensitizers relying on antibodies, lipid molecules, and metabolic labeling have gained effects, the development of simpler and stable methods that avoid complex chemical synthesis and biosynthesis steps is still a huge challenge. Here, the study has introduced 2D nanomaterials with the ability of cell surface engineering to perform the in situ anchoring of photosensitizer on living cell surface.

Modular synthesis of triphenylphosphine-derived cage ligands for rhodium-catalyzed hydroformylation applications.

Four new triphenylphosphine-derived cage ligands were modularly synthesized dynamic imine chemistry (DIC), and their absolute structures were characterized by single crystal X-ray diffraction (SXRD), nuclear magnetic resonance (NMR) and high resolution mass spectroscopy (HRMS). In contrast to small-molecule analogues, cage ligands demonstrate superior activity and selectivity. The Rh/Cage-L2 catalyst exhibits remarkable performance with an aldehyde selectivity of 89%, accompanied by a TOF value of 2665 h and an / ratio of 2.

Carbazolyl-Decorated Metal-Organic Framework with a High Fluorescent Quantum Yield for Detection and Photocatalytic Degradation of Organic Contaminants.

A carbazolyl-based fluorescent metal-organic framework with deep-blue light emission and a high quantum yield (88%) has been screened out by changing the ratio of mixed ligands, named Cz-MOF-2, which was constructed by ZrO(OH) clusters, 3-(9-ethyl-9-carbazol-3-yl)-4-methylthieno[2,3-]thiophene-2,5-dicarboxylate (HECMTDC) and 3,4-dimethyl-dihydrothieno[2,3-]thiophene-2,5-dicarboxylate (HDMTDC). Cz-MOF-2 has excellent sensitivity in fluorescent sensing of 2,6-dichloro-4-nitroaniline (DCN), nitrofurazone (NZF), and nitrofurantoin (NFT) with detection limits of 3.37 × 10, 1.

Inorganic Salt Solution-Based Aerosols for Fabricating Honeycomb-Patterned Porous Membranes.

Porous membranes with uniform pore sizes have shown potential applications. Although the breath figure method is renowned for its simplicity, it requires high humidity conditions, presenting challenges in energy consumption and safety, especially in arid climates. This study introduces an approach that uses inorganic salt-based aerosols to successfully fabricate honeycomb-patterned porous membranes at low humidity levels, where pure water vapor cannot produce such structures.

Investigation on the combustion mechanism for NF/H in DF/HF chemical lasers: a new perspective based on deep potential molecular dynamics simulations.

Combustion-driven deuterium fluoride/hydrogen fluoride (DF/HF) lasers are a crucial type of chemical lasers. Their chemical efficiency mainly depends on the production efficiency of atomic fluorine in the combustion chamber, where NF serves as the fluorine resource, and H acts as the reducing agent. However, due to the complex combustion process, high reaction temperatures, and potent corrosiveness of the products, the combustion mechanism of NF/H in the combustion chamber is still not fully revealed, including the chemical details of F atom generation.

Ion osmolarity-driven sequential concentration-enrichment for the scale-up isolation of extracellular vesicles.

Extracellular vesicles (EVs) carry a variety of bioactive molecules and are becoming a promising alternative to cell therapy. Scale-up EV isolation is necessary for their functional studies and biological applications, while the traditional methods are challenged by low throughput, low yield, and potential damage. Herein, we developed an ion osmolarity-driven sequential concentration-enrichment strategy (IOSCE) for the EV isolation.

Engineering organoids-on-chips for drug testing and evaluation.

Organoids-on-chips is an emerging innovative integration of stem cell-derived organoids with advanced organ-on-chip technology, providing a novel platform for the in vitro construction of biomimetic micro-physiological systems. The synergistic merger transcends the limitations of traditional drug screening and safety assessment methodologies, such as 2D cell cultures and animal models. In this review, we examine the prevailing challenges and prerequisites of preclinical models utilized for drug screening and safety evaluations.

Achieving Dendrite-Free Lithium Metal Batteries by Constructing a Dense Lithiophilic CuSe/CuO Heterojunction Tip.

Lithium (Li) metal batteries (LMBs) have garnered widespread attention due to their high specific capacity. However, the growth of lithium dendrite severely limits their practical applications. Herein, a novel strategy is proposed to regulate the overall potential strength and lithium ions (Li) concentration on the surface of the current collector by utilizing densely distributed tip effects.