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Delocalized radical systems are appealing for controlling stereoselectivity in organic synthesis. Here the authors report on a Co(II)-based enantioselective radical system for the dearomative 1,7-conjugate amination of readily available 4-vinylphenols with aryl azides.

Experiments under upper-tropospheric conditions map the chemical formation of isoprene oxygenated organic molecules (important molecules for new particle formation) and reveal that relative radical ratios control their composition

A post-translational backbone extension acyl rearrangement (BEAR) reaction has now been developed that converts a ribosomal protein product into a new product containing a β-peptide, γ-peptide or δ-peptide backbone. BEAR reactions represent a general strategy to install extended backbones into genetically encoded proteins and peptides expressed in cells.

Battery recyclability presents a sustainability challenge in materials design. Now it has been shown that aramid amphiphile self-assembly yields solid-state electrolytes with fast ion conductivity and electrochemical stability, which disassemble to the monomeric state upon solvent exposure, enabling inherently recyclable, molecularly engineered battery designs.

The authors advance the foundations of exciton-polariton transport based on a field-theoretical approach. This provides microscopic insight on the experimentally observed group velocity renormalization effect.

Self-assembled multidomain supramolecular peptide hydrogels that engage in dynamic covalent bonding with small-molecule drugs and biologics are shown to offer sustained release, extend the activity, and maintain safe and potent drug levels in vivo.

While Bell inequalities have been violated several times—mostly in photonic systems—their violations within particle physics experiments are less explored. Here, the BESIII Collaboration showcases Bell-violating nonlocal correlations between entangled hyperon pairs.

The authors perform heating experiments using femtosecond X-ray free electron laser pulses to explore the phase stability of superionic H₂O. The absence of a face-centered cubic phase below 50 GPa, where superionic ice forms from the melt, is attributed to the short heating time and may help understanding the stability of superionic phases in ice-rich planets.

Perovskite manganites exhibit intriguing but poorly understood properties, including multiferroicity. Here, the authors synthesize a Ce₃Mn₈ cluster that structurally resembles a perovskite repeat unit, and use this molecular analogue to elucidate mechanisms driving bulk perovskite properties.

Entanglement was observed in top–antitop quark events by the ATLAS experiment produced at the Large Hadron Collider at CERN using a proton–proton collision dataset with a centre-of-mass energy of √s  = 13 TeV and an integrated luminosity of 140 fb⁻¹.

The cleavage of C–C bonds in hydrocarbons is traditionally entrusted to precious metal catalysts, whereas common non-reducible oxides are considered unreactive. Now, the authors report nanostructured silica-embedded zirconia nanoparticles that are competent for the hydrogenolysis of polyethylene with remarkable performance.

Glutathione-capped copper–indium–selenium nanotubes that display phosphorescence in acidic environments facilitate enhanced tumour-specific imaging in the second near-infrared spectral window.

Enantioselective C–H amination is an attractive strategy for the synthesis of chiral amines. Now, a combined radical and ionic approach has been developed for 1,2-difunctionalization of alcohols by merging enantioselective radical C–H amination with stereospecific nucleophilic ring-opening, enabling synthesis of β-functionalized chiral amines.

Electrocatalytic CO₂ reduction into multicarbon products offers a means to close the anthropogenic carbon cycle using renewable electricity. Here, the authors report a cascade AgCu single-atom and nanoparticle electrocatalyst with favorable properties to improve the selectivity of multicarbon products.

The semileptonic decay channels of the Λc baryon can give important insights into weak interaction, but decay into a neutron, positron and electron neutrino has not been reported so far, due to difficulties in the final products’ identification. Here, the BESIII Collaboration reports its observation in e+e- collision data, exploiting machine-learning-based identification techniques.

Surface dynamics play a central role in the biological function of natural supramolecular structures. Here, the authors investigate the nanoscale dynamics at the surface of synthetic nanostructure using binding affinity to surface bound chelators.

A new methodology for the discovery of chalcogenides by tuning the temperature and flux ratios of systems using mixed fluxes is demonstrated, leading to the synthesis of 30 new and unreported compounds or compositions.

Preparing two-dimensional heterolayers by vertically stacking chemically different layers with multiple anions remains challenging. Now, a general approach for the synthesis of heterolayered oxychalcogenides using molten hydroxides as unconventional solutions for the rapid stacking of oxide and chalcogenide layers with precise composition control is demonstrated.

Investigating the inner structure of baryons is important to further our understanding of the strong interaction. Here, the BESIII Collaboration extracts the absolute value of the ratio of the electric to magnetic form factors and its relative phase for e + e − → J/ψ → ΛΣ decays, enhancing the signal thanks to the vacuum polarisation effect at the J/ψ peak.

Effective band-gap engineering of armchair graphene nanoribbons calls for control over both width and edge structure. Here, the authors report a modular synthesis of narrow N = 6 armchair graphene nanoribbons whose edges can be unsymmetrically modified with heteroarenes, introducing a simple way to tune band gap.

Cobalt(II) complexes of porphyrins have dominated the development of metalloradical catalysts. Now it has been shown that five-coordinate iron(III) complexes of porphyrins with an axial ligand are also potent metalloradical catalysts for olefin cyclopropanation. They are shown to react with different classes of diazo compounds via a stepwise radical mechanism.

An Ni-electrocatalytic system can couple two different carboxylates using doubly decarboxylative cross-coupling, tolerating a range of functional groups, being scalable, used for the synthesis of 32 known compounds and reducing overall step counts by 73%.

Olivine iron phosphate (FePO₄) is widely proposed for electrochemical lithium extraction, but particles with different physical attributes demonstrate varying Li preferences. Here, the authors characterize the electrochemical lithiation and sodiation behavior of a series of FePO₄ particles with different morphology to identify critical features that enhance Li selectivity.

Single-atom catalysts demonstrate enhanced catalytic properties, but most systems only explore combinations of a few different metals. Here, a library of 37 different elements is investigated, and it is shown that loading 12 metallic atoms in one system presents improved electrochemical activity.

Controlling various selectivities in radical reactions presents both formidable challenges and great opportunities. Now, Co(II)-based metalloradical catalysis has enabled the concurrent control of multiple convergences and selectivities in intermolecular radical allylic C−H amination. The reaction provides access to valuable chiral α-tertiary amines directly from an isomeric mixture of alkenes.

Catalysis with non-precious metals presents many advantages including ease of availability, security of supply and low cost. Here, the authors report a metal–organic framework with cobalt or iron sites for use as single-site solid catalysts in a number of chemoselective reactions.

Synthesizing superstructures with precisely controlled nanoscale building blocks is challenging. Here the assembly of superstructures is reported from atomically precise Ce₂₄O₂₈(OH)₈ and other rare-earth metal-oxide nanoclusters and their multicomponent combinations. A high-temperature ligand-switching mechanism controls the self-assembly.

Topological spin textures, such as skyrmions and antiskyrmions are of interest for use in information storage, owing to their inherent robustness. Critical to this use is the ability to manipulate these spin textures. Here, Yasin et al. demonstrate heat current driven transformation of a topological spin texture in a ferromagnet at room temperature.

Machine learning is a powerful tool for screening electrocatalytic materials. Here, the authors reported a seamless integration of machine-learned physical insights with the controlled synthesis of structurally ordered intermetallic nanocrystals and well-defined catalytic sites for efficient nitrate reduction to ammonia.

In laser-driven inertial fusion, finding optimal driving pressure is a major challenge. Here, the authors use a 100 kJ SG laser and a hybrid-drive scheme to demonstrate such driving pressure with the help of the direct-drive laser such that the indirect-drive radiation ablation pressure is turned into a well-smoothed hybrid-drive pressure much greater than the radiation ablation pressure.

The transport behavior of the carriers residing in the lowest Landau level is hard to observe in most topological materials. Here, Liu et al. report a surprising angular dependence of the interlayer magnetoresistivity and Hall conductivity arising from the lowest Landau level under high magnetic field in type II Weyl semimetal YbMnBi₂.

Studying the nature of actinide-actinide bonds is important for understanding the electronic structure of the 5f elements, but the synthesis of these chemical bonds remains extremely challenging. Here, the authors report a strong covalent Th-Th bond formed between two rarely accessible Th³⁺ ions, stabilized inside a fullerene cage.

The inclusion of platinum-group metals for CO2 reduction electrocatalyst design may trigger the unwanted hydrogen evolution reaction. However, here the authors show that single-atom Pd and Pt on facet-selective Cu can selectively boost CO2 to CH4 or C2H4 conversion through dual-site pathways.

Strategies for biological membrane engineering have been proposed to enhance their anti-clearance efficiency and improve their clinical translation potential. Here the authors design nanoparticles coated with low-cholesterol membranes from T cells overexpressing PD1, showing reduced clearance in the blood and improved anti-tumor efficacy when loaded with a STING agonist and a photothermal agent.

The ATLAS experiment at the Large Hadron Collider reports a search for charged-lepton-flavour violation in decays of Z bosons into a τ lepton and an electron or muon of opposite charge.

Self-assembled nanoribbons with extensive and collective intermolecular interactions exhibit robust mechanical properties, enabling their translation to macroscopic solid-state threads.

The ATLAS Collaboration reports the observation of the electroweak production of two jets and a Z-boson pair. This process is related to vector-boson scattering and allows the nature of electroweak symmetry breaking to be probed.

The ATLAS Collaboration reports a measurement of the ratio of the decay rates of W bosons to τ leptons and muons, in agreement with universal lepton couplings as postulated in the standard model of particle physics.

A new family of tunable microwave dielectrics with unparalleled performance at frequencies up to 125 GHz at room temperature has been created, using dimensionality to add and control a local ferroelectric instability in a system with exceptionally low dielectric loss.

Symmetry breaking in colloidal crystals is achieved with DNA-grafted programmable atom equivalents and complementary electron equivalents, whose interactions are tuned to create anisotropic crystalline precursors with well-defined coordination geometries that assemble into distinct low-symmetry crystals.

Quantum electrodynamics predicts a rare process in which light is scattered by light. The ATLAS Collaboration reports signs of this elusive effect in the collisions of ultra-relativistic lead ions.

Many aspects of materials chemistry rely on singlet–triplet spin conversion, but spin–vibronic effects are shown to accelerate the process when vibronic coupling causes the quantum-mechanical mixing of spin states.

Macrocycles are molecular structures extensively used in the design of catalysts, therapeutics and supramolecular assemblies but synthesis procedures that can produce macrocycles in high yield under high reaction concentrations are rare. Here the authors report the use of dynamic hindered urea bond for the construction of urea macrocycles with high efficiency.

Silicon microring resonator plays crucial role in optical computing owing to the compact footprint and energy-efficiency, yet existing modulators require >2 V to drive it. Here, the authors present a solution to this by using metal-oxide-semiconductor capacitor microring that brings down the driving voltage to 0.8 V.

Experimental work and computational modeling together reveal a suite of catalytic roles of the GlcN6P cofactor in the glmS ribozyme, including activation of the nucleophile, electrostatic stabilization, and alignment of the active site.

Understanding mechanisms of PLpro substrate selectivity offers new ways to decouple substrate activities and will inform new therapeutic strategies. Here, the authors use multi-disciplinary approaches to uncover how PLpro from SARS-CoV-2 can discriminate between different substrates.