Core Structure Research Articles

Access to 2,4-Disubstituted Pyrrole-Based Polymer with Long-Wavelength and Stimuli-Responsive Properties via Copper-Catalyzed [3+2] Polycycloaddition.

Pyrrole-based polymers (PBPs), a type of fascinating functional polymers, play a crucial role in materials science. However, efficient synthetic strategies of PBPs with diverse structures are mainly focused on conjugated polypyrroles and still remain challenging. Herein, an atom and step economy protocol is described to access various 2,4-disubstituted PBPs by in situ formation of pyrrole core structure via copper-catalyzed [3+2] polycycloaddition of dialkynones and diisocyanoacetates. A series of PBPs is prepared with high molecular weight (Mw up to 18 200 Da) and moderate to good yield (up to 87%), which possesses a fluorescent emission located in the green to yellow light region. Blending the PBPs with polyvinyl alcohol, the stretchable composite films exhibit a significant strengthening of the mechanical properties (tensile stress up to 59 MPa, elongation at break >400%) and an unprecedented stress-responsive luminescence enhancement that over fourfold fluorescent emission intensity is maintained upon stretching up to 100%. On the basis of computational studies, the unique photophysical and mechanical properties are attributed to the substitution of carbonyl chromophores on the pyrrole unit.

Energy absorption and low-velocity impact responses of the sandwich panels with lattice truss core

This study investigates the dynamic energy absorption performance of composite sandwich panels with two different configurations of lattice truss core. Two types of core structures were designed and created using polyamide 12 through the selective laser sintering (SLS) additive manufacturing method. These structures, with uniform and graded cell topologies, were created by changing the geometry and layer density of the body-centered cubic (BCC) unit cell. The cores were used to fabricate composite sandwich panels, which were made with E-glass/epoxy face sheets. Then, their ability to absorb energy during low-velocity impact and quasi-static compressive strength was tested using both experimental and numerical methods. It was found that the graded structure absorbed 10, 5, and 3% more energy than the uniform structure for the energy levels of 12.4, 16.5, and 17.9 J, respectively. It was also found that both structures could absorb at least 90% of the impact energy. In terms of strength, the uniform structure was able to tolerate 1.15 times larger impact loads, indicating its higher strength than the graded structure. The uniform structure had 8% more compressive strength.

Study on Influence of Core Structure on Catalytic Converter Performance Using CFD

In recent years, as the automotive industry is growing, one of the major hope for future vehicles is to meet emissions regulations. Automobiles pollute the air, and clean-air laws have made Catalytic Converters a legal requirement because they convert harmful pollutants from an engine's exhaust into cleaner emissions. The device works with the principle of a catalyst, something that causes or speeds up a chemical reaction without itself being changed. But the presence of a catalytic converter increases the exhaust back pressure which has an indirect effect on the engine efficiency ie engine efficiency decreases, thus increasing fuel consumption. The performance of a catalytic converter is substantially affected by the flow distribution inside the substrate, a uniform flow distribution can increase its efficiency, lower the pressure drop and optimize engine performance. The flow distribution in a catalytic converter assembly 15 is governed by the geometry configurations of the inlet and outlet cone section, the substrate, and exhaust gas compositions, and therefore a better design of the catalytic converter is very important. This Project deals with the fundamental understanding and study of complex processes taking place involving fluid flow, pressure, and velocity profiles in the catalytic converter using ANSYS WORKBENCH 2022 R1. The main objective of our analysis is to determine the most effective and optimum design of a Catalytic Converter

Synthesis, structure and electrochemical properties of Co-MOF containing pyridine polycarboxylic acid

Metal-organic frameworks (MOFs) have been widely used in filed of electrochemistry. Compared with traditional inorganic porous materials, the polyvalent pyridinecarboxylic acid ligands have many advantages which contains more active sites, flexible coordination mode, adjustable structure. Therefore, it becomes good choice for constructing MOFs materials with excellent performance. In this paper, a novel MOF was synthesized by pyridine polycarboxylic acid ligand and CoCl2·6H2O using solvothermal method. The physicochemical properties were characterized by FT-IR, powder diffraction and thermogravimetry. Single crystal X-ray diffraction reveal that MOF-1 crystallizes in monoclinic system with P21/C space group. The central Co2+ ions have a dual core structure with 5 and 6 coordination, respectively. The carboxyl groups show two kinds of coordination modes μ2: η1: η1 and μ2: η1: η2, and the pyridine N atoms also coordinate to form a three-dimensional network structure. Electrochemical experiments show that MOF-1 has a lower overpotential (339.4 mV) and Tafel slope (65.3 mV·dec−1) with higher ECSA and better OER kinetics. A large number of exposed active sites indicate that the MOF has higher potential as catalyst for oxygen evolution reaction.

Achieving exceptional combination of strength and ductility in α+β diphase brass with harmonic structure

Heterogeneous structures are an effective way to give materials excellent combined strength-ductility properties. In this study, Cu–Zn–Al–Fe alloys were prepared by homogenizing and hot rolling-annealing, and an α+β diphase brass with harmonic structure was obtained by adjusting the content of Zn. The microstructure and mechanical properties of Cu-xZn-4Al-2.8Fe (x = 14, 20, 22.5, 24, wt%) were systematically investigated. The Cu–Zn–Al–Fe alloy has an α single-phase matrix at 14 wt% Zn and an α+β diphasic matrix at 20, 22.5, and 24 wt% Zn, all uniformly distributed with nano β(FeAl). A large amounts of twins are produced after rolling in α phase that has a low stacking fault energy. The Cu–20Zn–4Al-2.8Fe alloy exhibits a unique harmonic structure of the α-phase soft cores embedded in α+β biphasic hard shells. This alloy exhibits an excellent strength-ductility combination at room temperature, possessing an ultimate tensile strength of 473.7 MPa while maintaining a total elongation of 50.7%. Increases total elongation by 30.3% while maintaining high strength compared to homogeneous alloys (22.5 wt% Zn). While α single-phase alloy (14 wt% Zn) exhibits excellent plasticity (total elongation of 58.0%), their strength is not satisfactory (ultimate tensile strength of 419.7 MPa). In contrast, too much Zn (24 wt% Zn) produces a high proportion of β phase, which exhibits high strength (ultimate tensile strength of 507.9 MPa) and relatively poor plasticity (total elongation of 22.8%). Overall, the Cu–20Zn–4Al-2.8Fe alloy with a harmonic structure achieves excellent overall mechanical properties due to twinning, precipitation strengthening, and hetero-deformation induced (HDI) strengthening. This study provides an essential reference for designing heterogeneous structures of brass alloys.

An optimised protocol for the expression and purification of adenovirus core protein VII

Adenovirus protein VII (pVII) is a highly basic core protein, bearing resemblance to mammalian histones. Despite its diverse functions, a comprehensive understanding of its structural intricacies and the mechanisms underlying its functions remain elusive, primarily due to the complexity of producing a good amount of soluble pVII. This study aimed to optimise the expression and purification of recombinant pVII from four different adenoviruses with a simple vector construct. This study successfully determined the optimal conditions for efficiently purifying pVII across four adenovirus species, revealing the differential preference for bacterial expression systems. The One Shot BL21 Star (DE3) proved favourable over Rosetta 2 (DE3) pLysS with consistent levels of expression between IPTG-induced and auto-induction. We demonstrated that combining chemical and mechanical cell lysis is possible and highly effective. Other noteworthy benefits were observed in using RNase during sample processing. The addition of RNase has significantly improved the quality and quantity of the purified protein as confirmed by chromatographic and western blot analyses. These findings established a solid groundwork for pVII purification methodologies and carry the significant potential to assist in unveiling the core structure of pVII, its arrangement within the core, DNA condensation intricacies, and potential pathways for nuclear transport.

Physical Correlations and Predictions Emerging from Modern Core-collapse Supernova Theory

In this paper, we derive correlations between core-collapse supernova observables and progenitor core structures that emerge from our suite of 20 state-of-the-art 3D core-collapse supernova simulations carried to late times. This is the largest such collection of 3D supernova models ever generated and allows one to witness and derive testable patterns that might otherwise be obscured when studying one or a few models in isolation. From this panoramic perspective, we have discovered correlations between explosion energy, neutron star gravitational birth masses, 56Ni and α-rich freezeout yields, and pulsar kicks and theoretically important correlations with the compactness parameter of progenitor structure. We find a correlation between explosion energy and progenitor mantle binding energy, suggesting that such explosions are self-regulating. We also find a testable correlation between explosion energy and measures of explosion asymmetry, such as the ejecta energy and mass dipoles. While the correlations between two observables are roughly independent of the progenitor zero-age main-sequence (ZAMS) mass, the many correlations we derive with compactness cannot unambiguously be tied to a particular progenitor ZAMS mass. This relationship depends on the compactness/ZAMS mass mapping associated with the massive star progenitor models employed. Therefore, our derived correlations between compactness and observables may be more robust than with ZAMS mass but can nevertheless be used in the future once massive star modeling has converged.

Multi‐Platform Observations of Severe Typhoon Koinu

AbstractSevere Typhoon Koinu passed south of Hong Kong on 8 and 9 October 2023, triggering the issuance of the Increasing Gale or Storm Signal No. 9, the second highest tropical cyclone (TC) warning signal in Hong Kong. Koinu was a difficult case for TC warning service due to its compact size and rather erratic movement over the coastal waters of Guangdong. To monitor Koinu's movement and wind structure, the Hong Kong Observatory utilized various observational platforms, including meteorological aircraft, ocean radar, and synthetic aperture radar on polar orbiting satellites. The paper presents major observations derived from these measurements. The aircraft probe and dropsonde data suggested boundary layer inflow, warm core structure, eyewall updraft, and high turbulence in the eyewall of the typhoon. The weather radar observations indicated the occurrence of a waterspout in the vicinity of the typhoon. Additionally, the study highlights the forecasting performance of the AI‐based Pangu‐Weather model, which could outperform the conventional global numerical weather prediction models in forecasting TC track in the region. The documentation of these observations aims to provide valuable references for weather forecasters and stimulate further research on forecasting this type of tropical cyclone.

The Production of Hollow Nanofibers from PBS / TPU Blends by Coaxial Electrospinning Method

In this study, the production of hollow Polybutylene Succinate (PBS)/Thermoplastic Polyurethane (TPU) nanofibers as biodegradable nanomaterials with improved mechanical properties were carried out by coaxial electrospinning method. The polymer solutions of pure PBS, pure TPU, and PBS/TPU blends (60/40, 40/60, 20/80 w/w) (as the shell) versus pure Polyvinylpyrrolidone (PVP) (as core) were put together for bi-component nanofibers production. The core structure of nanofibers was dissolved in distilled water. Thus, hollow nanofibers were obtained with the removal of PVP from the structure. Characterization studies (SEM, FTIR, and Tensile tests) of hollow nanofibers were performed. The morphological properties of PBS/TPU blends in ratios of 60/40 and 20/80 were observed as homogeneous and non-adhered fiber structures. It was determined that the hollow PBS/TPU (60/40) mat has the thinnest nanofibers. New bond formations within the interactions of substances as studied in the chemistry of blended electrospun webs were examined with FTIR analysis. Therewithal, this test showed the removal of PVP in the core of all nanofibers. It was observed that the adhered fibers increased the tensile stress and decreased the tensile strain at mechanical test results that were verified also by SEM views. It is suggested that the hollow nanofibers produced by this study can be used in the biomedical field as a biodegradable and breathable wound dressing.

The behavior of 12⟨111⟩ screw dislocations in W–Mo alloys analyzed through atomistic simulations

Analyzing plastic flow in refractory alloys is relevant to many different commercial and technological applications. In this study, screw dislocation statics and dynamics were studied for various compositions of the body-centered cubic binary alloy tungsten–molybdenum (W–Mo). The core structure did not appear to change for different alloy compositions, consistent with the literature. The pure tungsten and pure molybdenum samples had the lowest plastic flow, while the highest dislocation velocities were observed for equiatomic, W0.5Mo0.5 alloys. In general, dislocation velocities were found to largely align with a well-established dislocation mobility phenomenological model supporting two discrete dislocation mobility regimes, defined by kink-pair nucleation and migration and phonon drag, respectively. Velocities were observed to increase with temperature and applied shear stress and with decreasing kink-pair formation energies. The 50 at. % W alloy was found to possess the lowest kink-pair formation energy, consistent with its higher dislocation velocity. Furthermore, molybdenum segregation to the dislocation line was found to be thermodynamically favorable specifically at low temperatures and was observed to significantly delay the onset of dislocation glide and then generally enhance dislocation velocities thereafter. This behavior was explained by examining the energy landscape of dislocation glide. Furthermore, a segregation/de-segregation phase transition was observed to occur around 2500 K beyond which no preferential segregation to the dislocation was found. Overall, our findings suggest strong dependencies of plastic flow in W–Mo alloys on composition and elemental segregation, in agreement with the available literature, and may provide useful information to guide the design of next generation structural materials.

Magnetic porous microspheres enhancing the anaerobic digestion of sewage sludge: Synergistic free and attached methanogenic consortia

The addition of exogenous materials is a commonly reported method for promoting the anaerobic digestion (AD) of sludge. However, most exogenous materials are nano-sized and their use encounters problems relating to a need for continuous replenishment, uncontrollability and non-recyclability. Here, magnetic porous microspheres (MPMs), which can be controlled by magnetic forces, were prepared and used to enhance the methanogenesis of sludge. It was observed that the MPMs were spherical particles with diameters of approximately 100 µm and had a stable macroporous hybrid structure of magnetic cores and polymeric shells. Furthermore, the MPMs had good magnetic properties and a strong solid–liquid interfacial electron transfer ability, suggesting that MPMs are excellent carriers for methanogenic consortia. Experimental results showed that the addition of MPMs increased methane production and the proportion of methane in biogas from AD by 100.0 % and 21.2 %, respectively, indicating the MPMs notably enhanced the methanogenesis of sludge. Analyses of variations in key enzyme activities and electron transfer in sludge samples with and without MPMs in AD revealed that the MPMs significantly enhanced the activities of key enzymes involved in hydrolysis, acidification and methanation. This was achieved mainly by enhancing the extracellular electron transfer to strengthen the proton motive force on the cell membrane, which provides more energy generation for methanogenic metabolism. A careful examination of the variations in the morphology, pore structure and magnetism of the MPMs before and after AD revealed that the MPMs increased the prevalence of many highly active anaerobes, and that this did not weaken the magnetic performance. The microbial community structure and metatranscriptomic analysis further indicated that the acetotrophic methanogens (i.e., Methanosaeta) were mainly in a free state and that CO2-reducing methanogens (i.e., Methanolinea and Methanobacterium) mainly adhered to the MPMs. The above synergistic metabolism led to efficient methanogenesis, which indicates that the MPMs optimised the spatial ecological niche of methanogenic consortia. These findings provide an important reference for the development of magnetic porous materials promoting AD.

Library Synthesis of Cyclobutanol Derivatives by Hyperbaric [2+2] Cycloaddition Reactions

AbstractCyclobutanes are attracting a growing interest in medicinal chemistry because of their unique structure and potentially advantageous pharmacological properties. Specifically, 1,3‐disubstituted cyclobutanes have been explored as conformationally restricted propyl isosteres in drug development. In this study, a concise two‐diversification‐point library of 3‐amino‐3‐[(arenesulfonyl)methyl]cyclobutanols was synthesized through a hyperbaric [2+2] cycloaddition reaction between sulfonyl allenes and benzyl vinyl ether as the key step. Three different sulfonyl allenes were used for synthesizing the core structures that were further derivatized by the addition of up to seven amines. The amino groups were incorporated in a moderate to excellent diastereoselectivity through conjugate addition to the four‐membered‐ring scaffolds. Overall, this synthesis process demonstrates the potential for further chemical expansion and fragment growth in drug development.

Fluid based sandwich panel core structure for blast load mitigation

Researchers have extensively explored various approaches to enhance the blast resistance of structures, concentrating on optimizing structural designs and employing a wide range of materials. This research investigates the impact of incorporating water as a fluid within the core of tubular sandwich panels on blast mitigation effectiveness. The study systematically analyzes various panel configurations by altering key design parameters: the thickness of the face sheets, spacing between the core elements, and proportion of fluid within the core. These variables are scrutinized through metrics such as elastic strain energy, the amount of work applied externally, and the movement of the panel. Utilizing finite element analysis, 27 distinct numerical experiments were conducted to gather data. The findings demonstrate that panels with a water-filled core exhibit superior blast resistance compared to their non-fluid counterparts. Specifically, panels with completely filled cores showed the lowest levels of panel displacement and external work, whereas those with half-filled cores recorded the highest elastic strain energy. Furthermore, regression analysis revealed that plate thickness predominantly influences panel displacement and external work, whereas the fluid volume fraction within the core most significantly affects elastic strain energy. This study contributes to the understanding of fluid-structure interactions in blast-resistant design, offering valuable insights for optimizing structural defenses against blast impacts.

PTSA‐Catalyzed [3+2] Cycloaddition of in Situ Generated 3‐Ylidene Oxindoles with Coumarin‐Based N‐Phenyl Enamine Derivatives

AbstractBrønsted acid mediated [3+2] cycloaddition of coumarin‐based enamines with 3‐ylidene oxindoles generated in situ from 3‐hydroxy‐3‐aroylmethyl oxindoles enabled the synthesis of polyheterocyclic compounds with a pyrrolocoumarin core structure in a highly regioselective manner. The synthetic procedure is highly efficient and metal‐free, and no chromatographic purification of the products is required. The chromenopyrrole derivatives bearing an oxindole moiety formed as rapidly interconverting rotamers.

Prebiotic effect of galacto-N-biose on the intestinal lactic acid bacteria as enhancer of acetate production and hypothetical colonization.

Specific members of lactic acid bacteria, which are commonly used as probiotics, possess therapeutic properties that are vital for human health enhancement by producing immunomodulatory metabolites such as exopolysaccharides, short-chain fatty acids, and bacteriocins. The long residence time of probiotic lactic acid bacteria in the GI tract prolongs their beneficial health effects. Moreover, the colonization property is also desirable for the application of probiotics in mucosal vaccination to provoke a local immune response. In this study, we found that GNB could enhance the beneficial properties of intestinal lactic acid bacteria that inhabit the human GI tract, stimulating acetate production and promoting intestinal colonization. Our findings provide a rationale for the addition of GNB to lactic acid bacteria-based functional foods. This has also led to the development of therapeutics supported by more rational prebiotic and probiotic selection, leading to an improved healthy lifestyle for humans.

Selective Manipulation of Well-Defined Trinuclear Pd(II)-Complexes.

Several strategies are available to design well-defined multimetallic molecular entities bearing functional ligands. Substoichiometric exchange reactions in the coordination sphere of pre-existing multinuclear precursors are relatively underexploited in this context. Palladium(II) acetate is not a mononuclear compound in the solid state but rather exists as a trimer, i. e. [Pd3(OAc)6]. Although this material is ubiquitously used to synthesize mononuclear Pd species, it may principally also lend itself to selective exchange of some of the edge-sharing acetate units in its triangular motif, whilst keeping the overall multinuclear architecture intact. Strikingly, little is known about the controlled manipulation and substoichiometric substitution chemistry of this well-defined conglomerate. We herein conclusively demonstrate that, for the first time, the targeted exchange of two or four acetate units from the Pd3(acetate)6 platform is possible, thereby installing either one or two new tridentate ligands onto this trinuclear architecture. Follow-up exchange and substitution chemistry is available without disrupting the multimetallic nature of the core structure. New complexes 2-7 are all conclusively characterized using multinuclear NMR spectroscopy, UV-vis and IR spectroscopy as well as X-ray diffraction analysis.

Molecular Targets of the 5-Amido-Carboxamide Bumped Kinase Inhibitor BKI-1748 in Cryptosporidium parvum and HCT-8 Host Cells.

Cryptosporidium parvum is an apicomplexan parasite causing persistent diarrhea in humans and animals. Issuing from target-based drug development, calcium-dependent protein kinase 1 inhibitors, collectively named bumped kinase inhibitors (BKIs), with excellent efficacies in vitro and in vivo have been generated. Some BKIs including BKI-1748 share a core structure with similarities to the first-generation antiprotozoal drug quinine, which is known to exert notorious side effects. Unlike quinine, BKI-1748 rapidly interfered with C. parvum proliferation in the human colon tumor (HCT) cell line HCT-8 cells and caused dramatic effects on the parasite ultrastructure. To identify putative BKI targets in C. parvum and in host cells, we performed differential affinity chromatography with cell-free extracts from non-infected and infected HCT-8 cells using BKI-1748 and quinine epoxy-activated sepharose columns followed by mass spectrometry. C. parvum proteins of interest were identified in eluates from columns coupled to BKI-1748, or in eluates from both BKI-1748 and quinine columns. However, no C. parvum proteins could be identified binding exclusively to BKI-1748. In contrast, 25 BKI-1748-specific binding proteins originating from HCT-8 cells were detected. Moreover, 29 C. parvum and 224 host cell proteins were identified in both BKI-1748 as well as in quinine eluates. In both C. parvum and host cells, the largest subset of binding proteins was involved in RNA binding and modification, with a focus on ribosomal proteins and proteins involved in RNA splicing. These findings extend previous results, showing that BKI-1748 interacts with putative targets involved in common, essential pathways such as translation and RNA processing.

Dynamic modeling and experimental study of multi-coil composite core energy harvester

To improve the output performance and working bandwidth of the magnetic levitation energy harvester, a new structure of multi-coil composite core energy harvester was proposed and verified by numerical simulation and experiment. Firstly, the working mechanism of the energy harvester was analyzed. The dynamics model and COMSOL Multiphysics finite element analysis model were established to study the influence of magnetic field and coil position on the output characteristics of the energy harvester. Then, an experimental platform was built to verify the proposed new energy harvester, and the influence of coil position on the output power of the energy harvester was explored. Three kinds of coil thicknesses, two kinds of coil winding directions, six kinds of coil connection modes and two kinds of magnet distribution experiments were designed. Finally, the influence of suspended core mass on output performance was analyzed, and the energy harvester with or without magnetic liquid was tested by sweeping frequency to evaluate its output performance. The experimental results show that the magnetic field near the coil can be enhanced effectively, and the output performance of the whole system can be improved by the magnet mutual repulsion energy harvester with coil connection mode CM1 in a consistent coil direction. With the increase of composite core mass, the output voltage and power of the energy harvester also increase, but the peak frequency decreases. Compared with the energy harvester without magnetic liquid, the output power performance of the designed multi-coil composite core energy harvester is significantly improved by 29%, and the frequency bandwidth growth rate is 73%. The normalized power density can reach 134.26 μWcm−3g−2. The new structure of the multi-coil composite core provides important reference significance for designing a more efficient magnetic levitation energy harvester.

Amphiphilic block copolymers of poly(N-vinyl pyrrolidone) and poly(isobornyl methacrylate). Synthesis, characterization and micellization behaviour in selective solvents

Block copolymers of N-vinyl pyrrolidone (NVP) and isobornyl methacrylate (IBMA), PIBMA-b-PNVP, were prepared employing the RAFT polymerization technique. IBMA was polymerized first followed by the polymerization of NVP in the presence of a suitable fluoroalcohol to accelerate the crossover reaction. The copolymers were characterized by Size Exclusion Chromatography (SEC) and NMR spectroscopy. The thermal stability of these copolymers was studied via Thermogravimetric Analysis (TGA) and Differential Thermogravimetry (DTG), showing unique characteristics compared to the respective PIBMA and PNVP homopolymers. The micellization behavior was studied in THF, which is a selective solvent for the PIBMA blocks. The corresponding statistical copolymers, PNVP-stat-PIBMA were also examined to elucidate the effect of the macromolecular architecture on the micellar properties. Furthermore, the self-assembly behavior in aqueous solutions was studied for the PIBMA-b-PNVP block copolymers. Water is a selective solvent for the PNVP blocks. Static (SLS) and dynamic light scattering (DLS) were employed to study the micellar assemblies. The encapsulation of the hydrophobic compound curcumin within the micellar core of the micellar structures in aqueous solutions was investigated by UV–Vis spectroscopy and DLS measurements.

Combined effect of interstitial-substitutional elements on dislocation dynamics in nitrogen-added austenitic stainless steels

Combined addition of interstitial-substitutional elements has been acknowledged to contribute to the increase in the strengths of steels. For further improvements in mechanical properties, their atomic-scale interaction mechanisms with dislocations are required to be examined. In this study, both high-resolution transmission electron microscopy and atom-probe tomography were used to correlate interstitial-substitutional elements with dislocation characteristics in austenitic stainless steels. Three types of dislocation core structures are identified and associated with their strain fields as well as N and Cr atoms in the N-added steels. It is revealed that N atoms interact elastically with the dislocations, followed by the segregation of Cr atoms via the chemical interaction between N and Cr atoms. This insight significantly improves the understanding of the multiple alloying mechanism in metallic materials such as interstitial alloys and high-entropy alloys.