Stability Of Configurations Research Articles

Exploring thin-shell dynamics in regular charged black hole through T-duality

We present a thin-shell in the background of a regular charged static black hole solution in the presence of T-duality effects for the Einstein–Maxwell system. The thin-shell are developed by matching the inner and outer manifolds through the well-known Visser’s cut-and-paste approach. We produce three types of thin-shells with an outer regular charged black hole from T-duality and different choices of inner manifolds named: 1. Thin-shell (inner flat spacetime), 2. Thin-shell Garvastars (inner de Sitter spacetime), and 3. Thin-shell wormholes (inner regular charged black hole from T-duality) We evaluate the surface stresses of a thin layer of matter contents at a thin-shell through Lanczos equations and also develop equations of motion of these constructed configurations. We also explore thin-shell stability through linearized radial perturbations at equilibrium shell radius with barotropic and generalized Chaplygin equations of state. We show that the stability of respective configurations enhances in the presence of exterior charged BH from T-duality. We conclude that thin-shell Garvastars are more stable than thin-shell and thin-shell wormholes.

Organocatalytic hydrogen bond donor/Lewis base (HBD/LB) synthesis and chiroptical properties of thiabridged [5]helicenes.

Thiabridged [5]helicenes are obtained from thioaryl-N-phthalimido benzo[a]phenothiazines using a hydrogen bond donor/Lewis base organocatalytic approach. Resolution of [5]helicenes using either (1S)-(-)-camphanic acid as a chiral auxiliary or CSP-HPLC is reported. Thiabridged [5]helicenes show an exceptional configurational stability with racemization energy barriers higher than 40 kcal mol-1. Electronic circular dichroism and TD-DFT calculations permit the assignment of the absolute configuration, demonstrating that the sign of optical rotation is not easily related to the M or P structure. Separated enantiomers show circularly polarized luminescence with high dissymmetry ratio.

The stability of CsPb(BrxCl1-x)3 all-inorganic mixed halide perovskites.

The use of mixed halide perovskites in the preparation of blue light-emitting diodes (LEDs) is considered to be the most effective and direct approach. However, the introduction of chlorine (Cl) element might raise stability issues in the system and lead to low efficiency, thereby impeding the development of deep blue light-emitting diodes with high efficiency and stability. Determining the alloy concentration and the atomic distribution of bromine-chlorine (Br-Cl) mixed systems is essential for further application of deep blue light-emitting diodes. In this work, we have systematically investigated the stability of bromine-chlorine (Br-Cl) mixed alloy systems in various substitution configurations using high-throughput theoretical calculations. Based on this, we have examined the relationship between configuration stability and three aspects: the type of octahedra, the orientation of the octahedra and the Pb-X-Pb distortion angle in the configuration.

Helically chiral multiresonant thermally activated delayed fluorescent emitters and their use in hyperfluorescent organic light-emitting diodes.

Chiral multiresonant thermally activated delayed fluorescence (MR-TADF) materials show great potential as emitters in circularly polarized (CP) organic light-emitting diodes (CP-OLEDs) owing to their bright and narrowband CP emission. Here, two new chiral MR-TADF emitters tBuPh-BN and DPA-tBuPh-BN possessing intrinsically helical chirality have been synthesized and studied. The large steric interactions between the tert-butylphenyl groups not only induce the helical chirality but also provide a notable configurational stability to the enantiomers. Racemic mixtures of tBuPh-BN and DPA-tBuPh-BN show narrowband emission at 490 and 477 nm with full-width at half maximum (FWHM) of 25 and 28 nm and photoluminescence quantum yields, Φ PL, of 85 and 54% in toluene. The separated enantiomers of tBuPh-BN and DPA-tBuPh-BN show symmetric circularly polarized luminescence (CPL) with respective dissymmetry factors |g PL| values of 1.5 × 10-3 and 0.9 × 10-3. The hyperfluorescence organic light-emitting diodes (HF-OLEDs) with tBuPh-BN and DPA-tBuPh-BN acting as terminal emitters and 2,3,4,5,6-penta-(9H-carbazol-9-yl)benzonitrile (5CzBN) as their assistant dopant exhibited, respectively, maximum external quantum efficiencies (EQEmax) of 20.9 and 15.9% at 492 and 480 nm with FWHM of 34 and 38 nm. This work demonstrates a strategy for developing intrinsically helically chiral MR-TADF emitters possessing significant configurational stability, which can be used in HF-OLEDs.

Stochastic migrations of Marangoni surfers between two lobes of a dumbbell-shaped confinement.

We report an experimental investigation on the stochastic migration dynamics of Marangoni surfers (camphor-infused paper disks) between the two lobes of a dumbbell-shaped chamber. We characterize the migration dynamics using survival analysis of a configuration, wherein a configuration represents a distinct distribution of disks between the lobes. We observe that a configuration's stability decreases with increasing pairwise interactions. Consequently, the configuration with equal partitioning of disks between the lobes-that is exactly one-half of disks in each lobe for even-numbered systems but with one extra disk in either of the lobes for odd-numbered systems-has the lowest pairwise interactions, thus is always the most stable configuration. Furthermore, all configurations exhibit a stretched exponential decay with time, which is ascribed to a disk's activity decay with time or "aging"-a phenomenon validated by modeling a camphor disk as a chiral active particle (CAP) as initially proposed by Cruz et al.

Revealing the structure and electronic characteristics of Te-rich threshold switching materials for high-density integration

Most Ge-centered tetrahedrons in amorphous GeTe6 are formed by stable Ge–Te bonds, ensuring the stability of amorphous configurations.

Comparison of double chevron-cut and biplanar distal femoral osteotomy techniques: A biomechanical study.

This study aimed to compare the stability and mechanical properties of the double chevron-cut (DCC) and biplanar (BP) distal femoral osteotomy (DFO) techniques, along with analyzing their respective contact surface areas. Biomechanical testing was performed using sawbone and 3D modeling techniques to assess axial and torsional stability, torsional stiffness, and maximum torque of both osteotomy configurations. Additionally, 3D models of the sawbone femur were created to calculate and compare the contact surface area of the DCC, BP, and conventional single-plane DFO techniques. Axial stiffness and maximum strength did not significantly differ between the two osteotomy techniques. However, in terms of torsional properties, the DCC technique exhibited superior torsional stiffness compared to the BP group (27 ± 7.7 Nm/° vs. 4.5 ± 1.5 Nm/°, p = 0.008). Although the difference in maximum torque did not reach statistical significance (63 ± 10.6 vs. 56 ± 12.1, p = 0.87), it is noteworthy that the DCC group sawbone model exhibited fracture in the shaft region instead of at the osteotomy site. Therefore, the actual maximum torque of the DCC construct may not be accurately reflected by the numerical values obtained in this study. The contact surface area analysis revealed that the BP configuration had the largest contact surface area, 111% larger than that of the single-plane configuration. but 60% of it relied on the less reliable axial cut. Conversely, the DCC osteotomy offered a 31% larger contact surface area than the single-plane configuration, with both surfaces being weight-bearing. The DCC osteotomy exhibited superior mechanical stability, showing improved rotational stiffness and maximum torque when compared to the BP osteotomy. Although the BP osteotomy resulted in a larger contact surface area than the DCC osteotomy, both were larger than the conventional single-plane configuration. In clinical practice, both the DCC and BP techniques should be evaluated based on patient-specific characteristics and surgical goals.

Stability, electronic properties and CO adsorption properties of bimetallic PtAg/Pt(111) surfaces.

Aiming at a better fundamental understanding of the chemistry of bimetallic PtAg/Pt(111) surfaces, we have investigated the stability, electronic properties and CO adsorption properties of bimetallic PtAg surfaces, including pseudomorphic Ag film covered Pt(111) surfaces and PtxAg1-x/Pt(111) monolayer surface alloys, using periodic density functional theory calculations. The data provide detailed insights into the relative stabilities of different surface configurations, as indicated by their formation enthalpies and surface energies, and changes in their electronic properties, i.e., in the projected local densities of states and shifts in the d-band center. The adsorption properties of different Ptn ensembles were systematically tested using CO as a probe molecule. In addition to electronic ligand and strain effects, we were particularly interested in the role of different adsorption sites and of the local COad coverage, given by the number of CO molecules per Pt surface atom in the Ptn ensemble. Different from PdAg surfaces, variations in the adsorption energy with adsorption sites and with increasing local coverage are small up to one COad per Pt surface atom. Finally, formation of multicarbonyl species with more than one COad per Pt surface atom was tested for separated Pt1 monomers and can be excluded at finite temperatures. General trends and aspects are derived by comparison with comparable data for PdAg bimetallic surfaces. Fundamental insights relevant for applications of bimetallic Pt catalysts, specifically PtAg catalysts, are briefly discussed.

Dissection of Targeting Molecular Mechanisms of Celastrol-induced Nephrotoxicity via A Combined Deconvolution Strategy of Chemoproteomics and Metabolomics.

Celastrol (Cel), derived from the traditional herb Tripterygium wilfordii Hook. f., has anti-inflammatory, anti-tumor, and immunoregulatory activities. Renal dysfunction, including acute renal failure, has been reported in patients following the administration of Cel-relative medications. However, the functional mechanism of nephrotoxicity caused by Cel is unknown. This study featured combined use of activity-based protein profiling and metabolomics analysis to distinguish the targets of the nephrotoxic effects of Cel. Results suggest that Cel may bind directly to several critical enzymes participating in metabolism and mitochondrial functions. These enzymes include voltage-dependent anion-selective channel protein 1 (essential for maintaining mitochondrial configurational and functional stability), pyruvate carboxylase (involved in sugar isomerization and the tricarboxylic acid cycle), fatty acid synthase (related to β-oxidation of fatty acids), and pyruvate kinase M2 (associated with aerobic respiration). Proteomics and metabolomics analysis confirmed that Cel-targeted proteins disrupt some metabolic biosynthetic processes and promote mitochondrial dysfunction. Ultimately, Cel aggravated kidney cell apoptosis. These cumulative results deliver an insight into the potential mechanisms of Cel-caused nephrotoxicity. They may also facilitate development of antagonistic drugs to mitigate the harmful effects of Cel on the kidneys and improve its clinical applications.

Theoretical insights into the adsorption and gas sensing performance of Fe/Cu-adsorbed graphene.

The binding mechanism of gas molecules on material surfaces is essential for understanding adsorption and sensing performance. In the present study, we examine the interaction of some volatile organic compounds (VOCs), including HCHO, C2H5OH, and CH3COCH3, on pristine graphene and its Fe/Cu-adsorbed surfaces using first-principles calculations. The results indicate that the adsorption of these molecules on graphene is regarded as physisorption, while chemisorption is observed for Fe/Cu attached surfaces. The binding of sites on molecules and surfaces primarily involves hydrogen bonds for the pure form of graphene. In contrast, stable interactions occur at functional groups such as >CO, -OH with Fe/Cu atoms, as well as CC bonds of π-rings on modified structures of graphene. It is noticeable that stronger adsorption is observed in the case of Fe addition (Gr-Fe) compared to Cu (Gr-Cu), enhancing the gas adsorption and sensing performance on graphene. Remarkably, the graphene surfaces supported by Fe and Cu improved selectivity in detecting VOC molecules, particularly C2H5OH and CH3COCH3 for Gr-Fe, and HCHO for Gr-Cu. Quantum chemical analyses reveal that the Fe/Cu⋯O/C contacts are covalent interactions, contributing significantly to the stability of configurations and sensing properties of Fe/Cu-adsorbed graphene. In summary, the observed improvements in selectivity, enhanced adsorption strength, and the identification of crucial interactions at the surface offer valuable insights into designing highly efficient gas sensors and developing advanced sensing materials.

Studies on the Configurational Stability of Tropolone-Ketone-, Ester-, and Aldehyde-Based Chiral Axes.

Recent studies have revealed that tropolone-amide aryl C-C(O) rotational barriers are dramatically higher than those of analogous benzamide-based systems, and as a result, they have an increased likelihood of displaying high configurational stability. Studies on other tropolone-based chiral axes are important to assess the generality of this phenomenon. Herein, we describe a series of studies on the rotational barriers of tropolone-ketone, tropolone-ester, and tropolone-aldehyde chiral axes. These studies are complemented with computational modeling of the dynamics of these and analogous benzenoid variants to illuminate the impact that tropolone may have on aryl-C(O) configurational stability.

Enantioselective Synthesis of N-N Amide-Pyrrole Atropisomers via Paal-Knorr Reaction.

The catalytic asymmetric construction of monoheteroaryl N-N axially chiral compounds and chiral five-membered aryl-based scaffolds remains challenging. Herein, we present a highly efficient enantioselective synthesis of monoheteroaryl N-N atropisomers via an asymmetric Paal-Knorr reaction, affording a diverse array of N-N amide-pyrrole atropisomers with excellent enantioselectivities. Gram-scale synthesis and post-transformations of the product demonstrated the synthesis utility of this method. Racemization experiments confirmed the configurational stability of these N-N axially chiral products. This study not only provides the first de novo cyclization example for accessing an asymmetric monoheteroaryl N-N scaffold but also offers a new member of the N-N atropisomer family with potential synthetic and medicinal applications.

Dynamic quantitative phase imaging using calcite crystal-based temporally stable interferometer

This paper describes the development of a common path off-axis quantitative phase microscope (QPM), enabling high-speed quantitative measurements of sub-cellular dynamics in a live cell. The proposed 4f optical system consists of a polarizer, lenses, calcite crystal, pinhole and analyser, attached to the output port of an optical microscope converting it into a temporally stable QPM. The temporal phase stability of this optical configuration is measured to be equal to ∼20 mrad without a vibration isolation table. The utility of the microscope is demonstrated by conducting experiments on a polystyrene sphere (dia. 12 μm) and human red blood cells (RBCs). Furthermore, the developed system is implemented to study temporal membrane fluctuation in human RBCs over ∼30s and mouse embryonic fibroblast cell dynamics over 2 hours. Therefore, the system offers an energy-efficient and simple solution for generating object and reference beams for common-path QPM, making it an attractive alternative to existing approaches.

Bespoke Tailoring of Graphenoid Sheets: A Rippled Molecular Carbon Comprising Cyclically Fused Nonbenzenoid Rings.

The incorporation of nonbenzenoid rings into the hexagonal networks of graphenoid nanostructures is of immense importance for electronic, magnetic, and mechanical properties, but the underlying mechanisms of nonbenzenoid ring fusion are rather unexplored. Here, we report the synthesis and characterization of a rippled C84 molecular carbon, which contains 10 nonbenzenoid rings (five-, seven-, and eight-membered rings) that are contiguously fused to give a cyclic geometry. The fused nonbenzenoid rings impart high solubility, configurational stability, multiple reversible redox behaviors, unique aromaticity, and a narrow band gap to the system. Moreover, this carbon nanostructure allows for further functionalization via electrophilic substitution and metalation reactions, enabling access to finely tuned derivatives. Interestingly, both the bowl-shaped and planar conformations of the core in molecular carbon are observed in the solid state. Additionally, this molecular carbon displays ambipolar transport characteristics.

New 5-Substituted SN38 Derivatives: A Stability Study and Interaction with Model Nicked DNA by NMR and Molecular Modeling Methods.

The new 5-substituted SN-38 derivatives, 5(R)-(N-pyrrolidinyl)methyl-7-ethyl-10-hydroxycamptothecin (1) and its diastereomer 5(S) (2), were investigated using a combination of nuclear magnetic resonance (NMR) spectroscopy and molecular modeling methods. The chemical stability, configuration stability, and propensity to aggregate as a function of concentration were determined using 1H NMR. The calculated self-association constants (Ka) were found to be 6.4 mM-1 and 2.9 mM-1 for 1 and 2, respectively. The NMR experiments were performed to elucidate the interaction of each diastereomer with a nicked decamer duplex, referred to as 3. The calculated binding constants were determined to be 76 mM-1 and 150 mM-1 for the 1-3 and 2-3 complexes, respectively. NMR studies revealed that the interaction between 1 or 2 and the nicked decamer duplex occurred at the site of the DNA strand break. To complement these findings, molecular modeling methods and calculation protocols were employed to establish the interaction mode and binding constants and to generate molecular models of the DNA/ligand complexes.

O-Hydroxyarylphosphanes: Strategies for Syntheses of Configurationally Stable, Electronically and Sterically Tunable Ambiphiles with Multiple Applications.

o-Hydroxyarylphosphanes are fascinating compounds by their multiple-reactivity features, attributed to the ambident hard and soft Lewis- and also Brønstedt acid-base properties, wide tuning opportunities via backbone substituents with ±mesomeric and inductive, at P and in o-position to P and O also steric effects, and in addition, the configurational stability at three-valent phosphorus. Air sensitivity may be overcome by reversible protection with BH3 , but the easy oxidation to P(V)-compounds may also be used. Since the first reports on the title compounds ca. 50 years ago the multiple reactivity has led to versatile applications. This includes various P-E-O and P=C-O heterocycles, a multitude of O-substituted derivatives including acyl derivatives for traceless Staudinger couplings of biomolecules with labels or functional substituents, phosphane-phosphite ligands, which like the o-phosphanylphenols itself form a range of transition metal complexes and catalysts. Also main group metal complexes and (bi)arylphosphonium-organocatalysts are derived. Within this review the various strategies for the access of the starting materials are illuminated, including few hints to selected applications.

The Pseudo Jahn-Teller effect and NBO analysis for untangling the symmetry breaking in the planar configurations of M2X4+ (M = Si, Ge and X = Cl, Br, I): effect on electronic structure and chemical properties.

The Pseudo Jahn- Teller effect is a significant tool for evaluating molecular distortion and symmetry breaking. The PJT effect associated with NBO analysis can be a powerful method for studying the structural properties variations arising from D2h → C2h distortions. The theoretical studies on Si2X4+ and Ge2X4+ radical cations have been rare. The calculations have shown that C2h non-planar structures are more stable than planar structures with D2h symmetry. The [Formula: see text] PJTE problem of M2X4+ compounds is a result of the coupling between the ground B3u state and the exited B1u state in the Qb2g direction causes. Also, the difference in M and X atoms can affect the PJT instability of compounds. The findings of this work show that the energy gap between the ground and excited states that have D2h symmetry decreases from M2Cl4+ to M2I4+ and increases from Si2X4+ to Ge2X4+. In fact, there is a significant relationship between instability of high-symmetry configurations, geometric parameters, electron delocalization, chemical hardness, electronegativity, electrophilicity index, and PJT stabilization energies. These results may serve to evaluate the distortion of similar systems. The structures of Si2X4+ and Ge2X4+ are optimized by LC-BLYP, M06-2X, and B3LYP methods with def2-TZVPP basis set in GAMESS software. The details of the excited states of compounds are studied by the TD-DFT method. NBO analysis for planar and non-planar structures is carried out at B3LYP/def2-TZVPP level by the NBO 5. G program that demonstrates HOMO, LUMO, ED, bonding and antibonding orbital occupancies, bond order, and E2.

Drive-specific selection in multistable mechanical networks.

Systems with many stable configurations abound in nature, both in living and inanimate matter, encoding a rich variety of behaviors. In equilibrium, a multistable system is more likely to be found in configurations with lower energy, but the presence of an external drive can alter the relative stability of different configurations in unexpected ways. Living systems are examples par excellence of metastable nonequilibrium attractors whose structure and stability are highly dependent on the specific form and pattern of the energy flow sustaining them. Taking this distinctively lifelike behavior as inspiration, we sought to investigate the more general physical phenomenon of drive-specific selection in nonequilibrium dynamics. To do so, we numerically studied driven disordered mechanical networks of bistable springs possessing a vast number of stable configurations arising from the two stable rest lengths of each spring, thereby capturing the essential physical properties of a broad class of multistable systems. We found that there exists a range of forcing amplitudes for which the attractor states of driven disordered multistable mechanical networks are fine-tuned with respect to the pattern of external forcing to have low energy absorption from it. Additionally, we found that these drive-specific attractor states are further stabilized by precise matching between the multidimensional shape of their orbit and that of the potential energy well they inhabit. Lastly, we showed evidence of drive-specific selection in an experimental system and proposed a general method to estimate the range of drive amplitudes for drive-specific selection.

Analysis of beam ion driven Alfvén eigenmode stability induced by Tungsten contamination in EAST

Alfvén eigenmodes (AE) activity is observed in the EAST high β N and low BT discharge 93910, operation scenario dedicated to explore the ITER baseline scenario. AEs are triggered after the plasma is contaminated by Tungsten that causes an abrupt variation of the thermal plasma and energetic particles (EPs) profiles. The aim of the present study is to analyze the AE stability in the 93910 discharge using the gyro-fluid code FAR3d, identifying the AE stability trends by comparing the plasma before and after the Tungsten contamination. Tungsten contamination causes the destabilization of Toroidal AEs (TAE) and Energetic particle modes (EPMs) in the same frequency range and radial location with respect to the experimental observation and M3D-K/GTAW code results. Next, a set of parametric studies are performed to analyze the effect of the thermal plasma and EP parameters on the AE stability. The analysis indicates a lower EP β threshold for the AEs destabilization if the EP energy increases, an improved AE stability of on-axis NBI configurations due to the stronger continuum damping in the inner plasma region as well as a large enhancement of the EP drive as the thermal ion density increases due to a higher ratio of the EP and Alfven velocities. Consequently, the simulations indicate the increment of the thermal ion density after the Tungsten contamination could be the main cause of the AE/EPM destabilization.

Stability of coorbital planets around binaries

In previous hydrodynamical simulations, we found a mechanism for nearly circular binary stars, such as Kepler-413, to trap two planets in a stable 1:1 resonance. Therefore, the stability of coorbital configurations becomes a relevant question for planet formation around binary stars. For this work, we investigated the coorbital planet stability using a Kepler-413 analogue as an example and then expanded the parameters to study a general n-body stability of planet pairs in eccentric horseshoe orbits around binaries. The stability was tested by evolving the planet orbits for 105 binary periods with varying initial semi-major axes and planet eccentricities. The unstable region of a single circumbinary planet is used as a comparison to the investigated coorbital configurations in this work. We confirm previous findings on the stability of single planets and find a first order linear relation between the orbit eccentricity ep and pericentre to identify stable orbits for various binary configurations. Such a linear relation is also found for the stability of 1:1 resonant planets around binaries. Stable orbits for eccentric horseshoe configurations exist with a pericentre closer than seven binary separations and, in the case of Kepler-413, the pericentre of the first stable orbit can be approximated by rc,peri = (2.90 ep + 2.46) abin.