Magnetic Measurements Research Articles

A bis-Phenolate Carbene-Supported bis-μ-Oxo Iron(IV/IV) Complex with a [FeIV(μ-O)2FeIV] Diamond Core Derived from Dioxygen Activation.

The diiron(II) complex, [(OCO)Fe(MeCN)]2 (1, MeCN = acetonitrile), supported by the bis-phenolate carbene pincer ligand, 1,3-bis(3,5-di-tert-butyl-2-hydroxyphenyl)benzimidazolin-2-ylidene (OCO), was synthesized and characterized by single-crystal X-ray diffraction, 1H nuclear magnetic resonance, infrared (IR) vibrational, ultraviolet/visible/near-infrared (UV/vis/NIR) electronic absorption, 57Fe Mössbauer, X-band electron paramagnetic resonance (EPR) and SQUID magnetization measurements. Complex 1 activates dioxygen to yield the diferric, μ-oxo-bridged complex [(OCO)Fe(py)(μ-O)Fe(O(C═O)O)(py)] (2) that was isolated and fully characterized. In 2, one of the iron-carbene bonds was oxidized to give a urea motif, resulting in an O(CNHC═O)O binding site, while the other Fe(OCO) unit remained unchanged. When the reaction is performed at -80 °C, an intensively colored, purple intermediate is observed (INT, λmax = 570 nm; ε = 5600 mol L-1 cm-1). INT acts as a sluggish oxidant, reacting only with easily oxidizable substrates, such as PPh3 or 2-phenylpropionic aldehyde (2-PPA). The identity of INT can be best described as a dinuclear complex containing a closed diamond core motif [(OCO)FeIV(μ-O)2FeIV(OCO)]. This proposal is based on extensive spectroscopic [UV/vis/NIR electronic absorption, 57Fe Mössbauer, X-band EPR, resonance Raman (rRaman), X-ray absorption, and nuclear resonance vibrational (NRVS)] and computational studies. The conversion of the diiron(II) complex 1 to the oxo diiron(IV) intermediate INT is reminiscent of the O2 activation process in soluble methane monooxygenases (sMMO). Most importantly, the low reactivity of INT supports the consensus that the [FeIV(μ-O)2FeIV] diamond core in sMMO is kinetically inert and needs to open up to terminal FeIV═O cores to react with the strong C-H bonds of methane.

Hofmann Clathrates: A "Blue Box" Approach to Modulate Spin-Crossover Properties.

Hofmann coordination polymers (CPs) with cationic ligands provide an innovative strategy for recognizing π-electron-rich aromatic molecules - similar to the "little blue box". In this study, we demonstrate that hydroquinone molecules can be incorporated into these coordination polymers when redox-active bipyridinium derivatives are used as axial ligands. The insertion leads to a significant structural modification, resulting in a shift of the spin transition by 150 K and an approximate 23 % increase in volume, caused by the strong donor-acceptor π-π stacking interaction formed between the ligands and the guest molecule. These findings have been confirmed through temperature-dependent single crystal X-ray diffraction, magnetic measurements and optical reflectivity measurements.

Hofmann Clathrates: A “Blue Box” Approach to Modulate Spin‐Crossover Properties

AbstractHofmann coordination polymers (CPs) with cationic ligands provide an innovative strategy for recognizing π‐electron‐rich aromatic molecules – similar to the “little blue box”. In this study, we demonstrate that hydroquinone molecules can be incorporated into these coordination polymers when redox‐active bipyridinium derivatives are used as axial ligands. The insertion leads to a significant structural modification, resulting in a shift of the spin transition by 150 K and an approximate 23 % increase in volume, caused by the strong donor‐acceptor π‐π stacking interaction formed between the ligands and the guest molecule. These findings have been confirmed through temperature‐dependent single crystal X‐ray diffraction, magnetic measurements and optical reflectivity measurements.

Analysis of interference fringes in a long-wave infrared full Stokes polarimeter based on rotating waveplates

In the long-wave infrared (LWIR, 8–15 µm) band, the interference effect of polarization elements becomes an issue in polarimetry due to defects in the anti-reflective coatings. The paper describes an analysis and optimization method for the rotating-waveplates-based Stokes polarimeter, to eliminate interference fringes and improve polarization measurement accuracy in LWIR. An interference model was established based on the theory of polarized light and thin-film optics. Different modulation schemes were simulated and analyzed to obtain an optimized Stokes polarimeter, reducing the instrumental polarization to less than 1E-3. Furthermore, experimental validation was conducted by the Accurate Infrared Magnetic Field Measurements of the Sun (AIMS) telescope. The result shows that the instrumental polarization was less than 2E-3, consistent with the simulation.

Retinol-binding protein 4 is a potential biomarker of changes in lean mass in postmenopausal women.

Identifying biomarkers can help in the early detection of muscle loss and drive the development of new therapies. Research suggests a potential link between retinol-binding protein 4 (RBP4) and muscle mass, particularly in postmenopausal women. This study aimed to examine the association between baseline RBP4 levels and changes in appendicular lean mass (ALM), an indicator of muscle mass, in postmenopausal women. A 12-month follow-up period (n=153) included baseline and 12-month ALM assessments using DXA. ALM was normalized to squared height (ALMI). Baseline evaluations encompassed insulin resistance via HOMA-IR and immunoassay magnetic bead panel measurements of RPB4, IL-6, TNF-α, and IL-10. Postmenopausal women were categorized into higher (n=77) and lower (n=76) RPB4 groups based on baseline RPB4 values. Their changes in ALMI were compared using Mann-Whitney tests. General linear model was employed to evaluate the predictive power of baseline RBP4 for ALMI changes, adjusting for confounding variables: age, physical activity, smoking status, body fat, HOMA-IR, inflammatory markers (TNF-α and IL-6), and anti-inflammatory factor (IL-10). The higher RBP4 group exhibited a more pronounced reduction in ALMI compared to the lower RBP4 group (Higher RBP4 = -0.39kg/m2, 95% CI: -0.48 to -0.31kg/m2vs. Lower RBP4 = -0.24kg/m2, 95% CI: -0.32 to -0.15kg/m2, P=0.011). After adjusting for confounding factors, the association between baseline RBP4 changes and ALMI remained (b = -0.008, SE=0.002, P<0.001), indicating higher baseline RBP4 values linked to greater ALMI reduction. Our findings support RBP4 as a potential biomarker for changes in muscle mass in postmenopausal women.

Fermi surface and Lifshitz transitions of a ferromagnetic superconductor under external magnetic fields

Lifshitz transitions are being increasingly recognized as significant in a wide variety of strongly correlated and topological materials, and understanding the origin and influence of Lifshitz transitions is leading to deeper understanding of key aspects of magnetic, transport, or quantum critical behavior. In the ferromagnetic superconductor UCoGe, a magnetic field applied along the c axis has been shown to induce a series of anomalies in both transport and thermopower that may be caused by Lifshitz transitions. The need to understand the subtleties of the relationship between magnetism, superconductivity and a heavy-electron Fermi surface in the ferromagnetic superconductors makes it important to explore if and why a series of magnetic-field-induced Lifshitz transitions occurs in UCoGe. Here we report magnetic susceptibility measurements of UCoGe, performed at temperatures down to 45 mK and magnetic fields (μ0H||c) up to 30 T. We observe a series of clearly defined features in the susceptibility, and multiple sets of strongly field-dependent de Haas-van Alphen oscillations, from which we extract detailed field dependence of the quasiparticle properties. We complement our experimental results with density functional theory band structure calculations, and include a simple model of the influence of magnetic field on the calculated Fermi surface. By comparing experimental and calculated results, we determine the likely shape of the Fermi surface and identify candidate Lifshitz transitions that could correspond to two of the features in susceptibility. We connect these results to the development of magnetization in the system. Published by the American Physical Society 2024

Anion and Cation Dynamics in Mixed-Anion Hydroborate Na3(BH4)(B12H12): 1H, 11B, and 23Na NMR Studies

Sodium borohydride-closo-hydroborate Na3(BH4)(B12H12) exhibits high room-temperature ionic conductivity and high electrochemical stability. To study the dynamical properties of this mixed-anion compound at the microscopic level, we have measured the 1H, 11B, and 23Na nuclear magnetic resonance spectra and nuclear spin-lattice relaxation rates over the temperature range of 8–573 K. Our 1H and 11B spin-lattice relaxation measurements have revealed two types of reorientational jump motion. The faster motional process attributed to reorientations of the [BH4]− anions is characterized by an activation energy of 159 meV, and the corresponding reorientational jump rate reaches ~108 s−1 near 130 K. The slower process ascribed to reorientations of the larger [B12H12]− anions is characterized by an activation energy of 319 meV, and the corresponding reorientational jump rate reaches ~108 s−1 near 240 K. The results of the 23Na nuclear magnetic resonance measurements are consistent with the fast long-range diffusion of Na+ ions in Na3(BH4)(B12H12). The diffusive jump rate of Na+ is found to reach ~104 s−1 at 300 K and ~8 × 108 s−1 at 530 K. A comparison of these jump rates with the ionic conductivity data suggests the importance of correlations between diffusing ions.

Ta4SBr11: A Cluster Mott Insulator with a Corrugated, Van der Waals Layered Structure.

The compound Ta4SBr11 was prepared by a comproportionation reaction of tantalum bromide with tantalum and elemental sulfur. The crystal structure, as refined by single-crystal X-ray diffraction, is composed of clusters with Ta4S cores, arranged in corrugated van der Waals layers. Individual layers appear to be displaced relative to each other along one direction. Successful crystal growth in a melt of CsBr yielded black platelets of Ta4SBr11, which were used to investigate the electrical properties of the compound. The electronic structure was studied by diffuse reflectance infrared Fourier transform (DRIFT) spectroscopy and by density functional theory (DFT) band structure calculations, revealing this material to be a small-gap semiconductor. DFT results, in combination with magnetic susceptibility measurements, suggest that metallicity originating from the one unpaired Ta d electron per cluster is most likely suppressed by electronic correlations, forming a cluster Mott insulator.

Synthesis, structural study, antimicrobial activity and theoretical treatment of Cr(III), Ni(II), Pt(IV) and Zn(II) complexes with 2-hydroxy-4-Nitro phenyl piperonalidene

The complexes of the 2-hydroxy-4-Nitro phenyl piperonalidene with metal ions Cr(III), Ni(II), Pt(IV) and Zn(II) were prepared in ethanolic solution. These complexes were characterized by spectroscopic methods, conductivity, metal analyses and magnetic moment measurements. The nature of the complexes formed in ethanolic solution was study following the molar ratio method. From the spectral studies, monomer structures proposed for the nickel (II) and Zinc (II) complexes while dimeric structures for the chromium (III) and platinum (IV) were proposed. Octahedral geometry was suggested for all prepared complexes except zinc (II) has tetrahedral geometry, Structural geometries of these compounds were also suggested in gas phase by using hyper chem-8 program for the molecular mechanics and semi-empirical calculations. The heat of formation and binding energy for the prepared compounds was calculated by using PM3 and AMBER methods. The method of PM3 was used for evaluate the vibration spectra for the imine and starting material as authentic compound. Preliminary in vitro tests for antibacterial and antifungal activity show that most of the prepared compounds display good activity to (Staphylococcus aureus), (Escherichia coli) and (Candida albicans).

Effect of charge-discharge with higher capacitance performance of Ni-substituted CoFe2O4 magnetic nanoparticles for energy storage

In this work, we synthesized NixCo1-xFe2O4 (0 ≤ x ≤ 0.8) magnetic nanoparticles (MNPs) by using ultrasonication-assisted reverse chemical co-precipitation method. The X-ray diffraction (XRD) patterns confirm the single-phase with mixed spinel structure of the NixCo1-xFe2O4 (0 ≤ x ≤ 0.8) MNPs with the crystallite size range between 12 nm - 17 nm. The molecular dynamics and oleic acid coated Ni-substituted CoFe2O4 magnetic nanoparticles were confirmed by FTIR measurements. The surface composition of NixCo1-xFe2O4 (0 ≤ x ≤ 0.8) MNPs (Ni, Co, Fe and O) and their oxidation states were estimated using X-ray photoelectron spectroscopy. The NixCo1-xFe2O4 (0 ≤ x ≤ 0.8) MNPs are spherical in shape and polycrystalline in nature, confirmed by FESEM and HRTEM measurements. The Ni-substituted CoFe2O4 MNPs with higher zeta potential (ζ) from −24 mV to -41 mV with an increase in Ni concentration, signifies the stable colloidal stability due to the electrostatic repulsion between MNPs. The DC magnetization (M-vs-H) measurements reveal the ferrimagnetic behavior of NixCo1-xFe2O4 (0 ≤ x ≤ 0.8) MNPs, which suppress the saturation magnetization (MS) from 48.6 emu/g to 5.3 emu/g with the enhanced coercivity (HC) from 335 Oe to 1700 Oe with the substitution of Ni2+ ions is in corroboration with electron paramagnetic resonance (EPR) measurements. The enhanced EPR resonance field (Hres = 2335 Oe - 3261 Oe) with the substitution of Ni2+ ions is attributed to the generation of oxygen vacancies and defects, which are predominant in Ni0.8Co0.2Fe2O4, resulting in significantly enhanced electrochemical performance. Therefore, the three-electrode system was utilized to investigate the electrochemical properties of NixCo1-xFe2O4 (0 ≤ x ≤ 0.8) MNPs. The Ni-substituted CoFe2O4 MNPs have demonstrated significantly enhanced capacity retention of 77 % even after 5000 cycles in 1 M H2SO4 electrolyte solution. NixCo1-xFe2O4 (0 ≤ x ≤ 0.8) MNPs exhibit an excellent specific capacity (Cs) of 794.5 F/g at a current density of 1 A/g, signifies the rate of redox reaction at surface electrolyte interface (SEI) is greatly influenced by the surface to volume ratio. Thus, with the enhancement of Ni2+ ions, redox reaction kinetics might become more efficient resulting in the enhanced charge storage capacity.

Observing the evolution of the Sun's global coronal magnetic field over 8 months.

The magnetic field in the Sun's corona stores energy that can be released to heat plasma and drive solar eruptions. Measurements of the global coronal magnetic field have been limited to several snapshots. In this work, we present observations, using the Upgraded Coronal Multi-channel Polarimeter, that provide 114 magnetograms of the global corona above the solar limb spanning ~8 months. We determined the magnetic field distribution with altitude in the corona and monitored the evolution at different latitudes over multiple solar rotations. The field strength between 1.05 and 1.60 solar radii varies from <1 to ~20 gauss. A signature of active longitudes appears in the coronal magnetic field measurements. Coronal models are generally consistent with our observations, though they have larger discrepancies in high-latitude regions.

Investigation of structural and magnetic properties of Mg0.946Cu2.054O3 compound

The crystal structure of synthesized Mg0.946Cu2.054O3 compound was examined using Rietveld refinement of powder X-ray diffraction (XRD), revealing the presence of antisite defects in the form of substitution occupation of Mg atomic sites by Cu atoms upto ∼9 %. Detailed investigation by magnetic measurements around antiferromagnetic Néel transition around 95 K and below hints at the existence of paramagnetic component and short-range order due to presence of antisite defects, which is further supported by specific heat measurements.

UWB distance estimation errors in (non-)line of sight situations within the context of 3D analysis of human movement

Abstract Integrated Ultrawideband (UWB) and Magnetic Inertial Measurement Unit (MIMU) sensors are becoming popular for indoor localization applications, as a higher accuracy can be achieved than with just MIMU sensors. These integrated sensors could extend stability and accuracy in the field of 3D analysis of human movement (3D AHM) if they can deliver position estimates with an accuracy close to 1 cm. Achieving this high accuracy of 1 cm remains challenging, with most studies reporting position estimation errors around 5 cm, often due to Non-Line of Sight (NLOS) conditions and systematic UWB sensor distance estimation errors. Studying the distance error characteristic of UWB in situations of 3D AHM is essential to deal with these errors. While research on UWB distance errors in Line of Sight (LOS) and NLOS situations exists, few studies focus on the NLOS errors caused by the human body and were not in the relevant scenarios of 3D AHM. Therefore, this article examines UWB sensor performance and distance error characteristics in LOS and NLOS situations typical for the 3D AHM. Both the LOS and NLOS situations were studied in the typical 3D AHM distance range of 0.2 m to 2 m. The NLOS situations were studied first with a human subject as NLOS causing object and then with simulated human body segments (PVC pipes filled with water) of varying diameters. In LOS situations, consistent systematic bias errors were observed, along with incidental errors at specific positions in the room. In NLOS scenarios caused by the human and simulated body segments, a consistent and reproducible overestimation of distances was found. The reproducibility of these errors based on relative node and object positions suggests that systematic mitigation methods could significantly reduce errors, enabling more accurate and reproducible 3D human movement analysis.

Synthesis, Characterization and Identification of Mononuclear Transition Metals Complexes 1, 3-Bis-((5-methyl-1H-Imidazol-4-yl) Methyleneamino) Propan-2-ol Ligand

The ligand 1,3-bis-((5-methyl-1H-imidazol-4-yl)methyleneamino)propan-2-ol (H3L) derived from 1,3-diaminopropan-2-ol and 5-methyl-1H-imidazole-4-carbaldehyde has been synthetized and used to prepare five complexes in which the ligand acts in tetradentate fashion. Complexes formulated as [Mn(H3L)(H2O)2].2SCN (1), [(Co(H3L)].2SCN (2), [(Ni(H3L)].2SCN (3), [(Cu(H3L)(NO3)].(NO3).2H2O (4), and [(Zn(H3L)].2SCN (5) were synthesized by mixing an equimolar amount of an methanol solution containing the appropriate nitrate salt and KSCN, in 1:2 ratio, in the case of 1, 2, 3 and 5 and an ethanol solution containing the appropriate ligand H3L. The complex 4 has been synthetized in the absence of KSCN. In all the complexes the ligand acts in its neutral form and in tetradentate fashion, its hydroxy group remaining free and non-deprotonated. The ligand is coordinated to metal ion through two azomethine nitrogen atoms and two pyrazole sp2 nitrogen atoms. The complexes are characterized by elemental analysis, conductance and room temperature magnetic moments measurements, UV–Vis and IR spectroscopic studies. The structure of the copper(II) complex 4 is confirmed by X-ray diffraction. 4 crystallizes in the monoclinic space group P21/c with unit cell dimensions a = 8.5459 (3) Å, b = 10.9177 (3) Å, c = 22.4562 (6) Å, b = 96.954 (3)°, V = 2079.79 (11) Å3, Z = 4, R1 = 0.050 and wR2 = 0.131. The CuII cation in N4O inner is situated in a distorted square pyramidal environment.

Magnetic field measurement with temperature compensation based on a fiber ring microwave photonic filter and Vernier effect.

We proposed, a novel, to the best of our knowledge, magnetic field measurement with temperature compensation based on a fiber ring microwave photonic filter (FR-MPF) and a Vernier effect. The sensing head is made up by attaching the fiber Bragg grating (FBG) on the magnetostrictive material. Based on the wavelength division multiplexing, two FR-MPFs with different optical carriers can eliminate the influence of the temperature. The Linear chirped FBG (LCFBG) in the FR can transfer the magnetic field variation to the time delay change as well as the frequency shift. Two FR-MPFs with close free spectral ranges can implement the Vernier effect, which can improve the sensitivity. The experimental results show the sensitivity is 58.3 kHz/Oe and the magnification factor is 214. The proposed sensor has merits of high resolution, high sensitivity and low cross-sensitivity, which has potential applications requiring high precision detections.

Multifaceted insights into Cu(II) complexes with bis(benzimidazole) ligands: Structural investigation, theoretical studies, cytotoxicity evaluation, and antioxidant summarizing

In this study, the synthesized two new ligands, namely bis(1H-benzo[d]imidazole-1-yl) methane [L1] and 1,2-bis(1H-benzo[d]imidazole-1-yl) ethane [L2], from benzimidazole. They chose 1,2-dibromomethane and 1,2-dibromoethane as they are widely used in environmental catalysis and as ligands in conjugated configurations. The researchers were able to synthesize the Cu(II) complexes, [Cu(L1)2]Cl2 or [1] and [Cu(L2)2]Cl2 or [2], at room temperature. They used several analytical techniques, including elemental analysis, magnetic moment measurement, UV–visible spectroscopy, FT-IR spectroscopy, FT-Raman spectroscopy, NMR spectroscopy (including 1H, 13C, DEPT-135, HSQC, and HMBC techniques), ESI-MS analysis, thermogravimetric analysis, and ESR spectroscopy, to characterize the synthesized compounds. They found that the ESR spectra of complexes [1] and [2] suggest that both metal complexes have square planar coordination spheres. In the DFT study of the geometrical optimization of both complexes, the central plane consists of the Cu metal atom connected to four nitrogen atoms. The Cu–N bond lengths are measured at 2.194 Å for [1] and 2.176 Å for [2] whereas the FMO theory's slight reduction in the HOMO-LUMO gap for [2] suggests that it is more reactive and less stable compared to [1]. In addition, the researchers tested the effect of these compounds on human cervical cancer cell lines (HeLa) which showed significant cytotoxic effects under laboratory conditions. Complex [2] had a significant inhibitory impact on the growth of cancer cells. The researchers also assessed the antioxidant effects of the ligands and metal complexes using DPPH, OH, and NO assays and found that [2] had the most potent inhibitory effect on the radicals, with IC50 values of 36.11 μM (DPPH), 28.18 μM (OH), and 26.20 μM (NO).

Slow magnetic relaxation in rare μ2[sbnd]O-Bridged Holmium(III) and Erbium(III) chain compounds

Lanthanide chain compounds with slow relaxation of the magnetization (SRM) behavior have garnered wide attention due to their rich physical phenomena and wide applications. However, the study with non-Dy3+ ions are still rare, mainly due to the challenges in balancing single-ion magnetic anisotropy and intrachain exchange couplings. In this work, two new μ2O-bridged homospin chain compounds: [Ln(L)2(phen)(μ2OH)(μ2H2O)]n (Ln = Ho(1), Er(2), HL = 4-nitrobenzoic acid, phen = 1,10-phenanthroline), were synthesized under solvothermal conditions and fully characterized. Both compounds exhibit weak but effective intrachain couplings transmitted by single-O bridges, leading to Ising-like chain behavior. Dynamic magnetic measurements within the temperature range revealing this special chain behavior indicate that both compounds also exhibit SRM behavior. Such results suggest they could be categorized to the family of single-chain magnets, which are rarely reported for lanthanide compounds with non-radical ligands and non-Dy3+ systems.

A structural, magnetic and colloidal stability study of uncoated and silica coated iron oxide samples prepared in two different surfactants

The discovery of new magnetic materials of interest in the biomedicine field is a relevant topic in current research. For years, our research group has been investigating the obtaining and study of nanostructured magnetic samples that behave superparamagnetically to enable their transport in living organisms. We present here a study that summarizes the structural characteristics, magnetic behavior and stability of two Fe3O4 samples synthesized by coprecipitation that were dispersed using two different surfactants (oleylamine, OL, and oleic acid, OA), and two others prepared from the previous ones by reaction with tetraethyl orthosilicate (TEOS). The relationships between the surfactant used in the synthesis, the presence of a certain maghemite (γ-Fe2O3) content, the influence of silica shell thickness and magnetic behaviour of all samples were systematically studied by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), Mössbauer spectroscopy and H vs. M loops. Rietveld refinements of the XRD profiles confirmed a partial oxidation of the non-silica-coated samples and FTIR spectra of the uncoated samples showed a very strong broad metal-oxygen band and additional sets of bands from the different organic chains of the two surfactants. Individual particles with a mean diameter of 7 and 9 nm were distinguished in TEM images of uncoated magnetic samples. Mössbauer data indicated the presence of non-stoichiometric magnetite in all samples, in agreement with XRD refinements. Magnetic measurements confirmed the superparamagnetic behavior of all the samples. Highest negative zeta potential values are found for the silica covered samples in both acidic and basic medium, being Fe3O4-AO@SiO2 the best suited for the purposes of its dispersibility in future applications. Low polydispersity index (PDI) values confirmed the best stability and dispersibility of all samples investigated in tetrahydrofuran (THF).

Critical current density and AC magnetic susceptibility of high-quality FeTe0.5Se0.5 superconducting tapes

Iron telluride-selenium superconducting materials, known for their non-toxicity, ease of preparation, simple structure, and high upper critical fields, have attracted much research interest in practical application. In this work, we conducted electrical transport measurements, magneto-optical imaging, and AC magnetic susceptibility measurements on FeTe0.5Se0.5 superconducting long tapes fabricated via reel-to-reel pulsed laser deposition. Our transport measurements revealed a high critical current density that remains relatively stable even with increasing external magnetic fields, reaching over 1 × 105 A/cm2 at 8 K and 9 T. The calculated pinning force density indicates that normal point pinning is the primary mechanism in these tapes. The magneto-optical images demonstrated that the tapes show homogeneous superconductivity and uniform distribution of critical current density. The AC magnetic susceptibility measurements also confirmed their strong flux pinning nature of withstanding high magnetic field. Based on these characteristics, FeTe0.5Se0.5 superconducting tapes show promising prospects for applications under high magnetic field.

Microwave-Assisted, Preparation, Characterization, and Biological Activities of Schiff Bases Derived from 4-Aminoantipyrine with Acetonyl Acetone for Some New Rare-Earth Metals

Five new lanthanide complexes based on azomethine (Schiff bases) ligands have been synthesized, including La, Nd, Er, Gd, and Dy. Complexes were synthesized using the azomethine Schiff bases resulting from condensation reactions between 4-aminoantipyrine and acetonylacetone. The structural characteristics of azomethine obtained are characterized quantitatively and qualitatively through various techniques, including elemental analyses, magnetic susceptibility measurement, molar conductivity, infrared, ultraviolet absorption, GC-mass, and 1H- and 13C-NMR spectroscopy studies. The structural characteristics of Ln+3 complexes indicate that the complexes possess a composition of a specific type. Based on the elemental analyses, magnetic susceptibility measurement, molar conductivity, and ultraviolet absorption spectroscopy data, it can be inferred that the central metal ion is surrounded by a coordination number of 10, the general formula of [Ln(L)2(NO3)]·nNO3nH2O. The physical measurements confirmed that the synthesized complexes exhibit non-electrolyte behavior and paramagnetic properties. The antibacterial activity of the compounds was assessed in vitro against 4 pathogenic strains: E. coli, S. aureus, K. pneumoniae, and S. mutans. The evaluation was conducted using the agar disc spreading method. The results demonstrated that certain complexes exhibited significant antibacterial efficacy in comparison to the biological activity of the ligand.