Complex Ions Research Articles

Sensitive Detection and Visual Recognition of Jatrorrhizine Based on a Fluorescent Eu Coordination Polymer Probe

ABSTRACTBased on 4‐([2,2′:6′,2″‐terpyridin]‐4′‐yl) benzoic acid ligand (Htpba), a fluorescent lanthanide coordination polymer was successfully synthesized, namely, [Eu (tpba)3]n (1). The single‐crystal diffraction analysis shows that Eu3+ ions in complex 1 are alternately connected with tpba3− ligands to form a one‐dimensional chain structure, which further constitutes a three‐dimensional supramolecular architecture through the π···π interactions. Complex 1 demonstrated excellent stability of thermogravimetry; and displayed good fluorescence intensity in aqueous solution with a wide pH range. In this work, complex 1 was used as a fluorescence sensor for the detection of jatrorrhizine molecule (JAT). It was found that complex 1 had high sensitivity with the detection limit of 1.02 × 10−8 M, and simultaneously displayed specific selectivity and reutilization for the exploration of JAT molecule. The static quenching, the absorption competition, the electrostatic interactions, and the photo‐induced electron transfer process are responsible for the recognition mechanism of complex 1 with sensing JAT. It is worth mentioning that a fluorescent film based on complex 1 and a light‐emitting diode device coated with the powder of complex 1 were successfully fabricated, which could rapidly recognize JAT molecule with the naked eye further.

Effect of ANSA as an additive on electrodeposited Sn-Ag-Cu alloy coatings in deep eutectic solvent

This study investigates the electrodeposition of Sn-Ag-Cu ternary solder coating in a choline chloride-ethylene glycol DES using 1-amino-2-naphthol-4-sulfonic acid (ANSA) as an additive. The mechanism of ANSA was evaluated through UV–visible absorption spectroscopy, infrared spectroscopy, and CV. The results demonstrate that ANSA, as a multifunctional organic compound, influences the electrodeposition process through its sulfonic acid, amino, and naphthyl groups. When the ANSA concentration is below 600 ppm, its primary action is through an interfacial adsorption mechanism, where lone pairs of electrons on nitrogen and oxygen atoms adsorb onto the electrode surface, and the bulky naphthyl ring inhibits the formation of large deposits. As the ANSA concentration exceeds 600 ppm, complexation becomes the dominant mechanism, competing with the complexation of chloride ions (Cl−) in the choline chloride electrolyte. SEM analysis indicates that as the ANSA concentration increases, the deposited coatings become smoother, denser, and exhibit finer grain sizes. The Scharifker-Hills model was employed to analyze the CA curves before and after the addition of ANSA, revealing that the nucleation mechanism of Sn-Ag-Cu alloy deposition gradually transitions from instantaneous nucleation to progressive nucleation with increasing ANSA concentration.

Second order Rayleigh–Schrödinger perturbation theory for the Grasp2018 package: Core–core correlations

GRASP package is based on the relativistic configuration interaction in which accurate calculations, accounting for valence, valence–valence, core–valence, core and core–core electron correlations, often rely on massive CSF expansions. This paper presents a further development of the method based on the second-order perturbation theory for finding the most important CSFs that have the greatest influence on the core–valence, core and core–core correlations. This method is based on a combination of the relativistic configuration interaction method and the stationary second-order Rayleigh–Schrödinger many-body perturbation theory in an irreducible tensorial form [G. Gaigalas, P. Rynkun, and L. Kitovienė, Second-order Rayleigh–Schrödinger perturbation theory for the GRASP2018 package: Core–valence correlations, Lith. J. Phys. 64(1), 20–39 (2024), https://doi.org/10.3952/physics.2024.64.1.3, and G. Gaigalas, P. Rynkun, and L. Kitovienė, Second-order Rayleigh–Schrödinger perturbation theory for the GRASP2018 package: Core correlations, Lith. J. Phys. 64(2), 73–81 (2024), https://doi.org/10.3952/physics.2024.64.2.1]. In this extension, the perturbation theory takes into account electron core–valence, core and core–core correlations, where an atom or ion has any number of valence electrons, for calculation of energy spectra and other properties. Meanwhile, the rest of the correlations are taken into account in a traditional way. This allows a significant reduction of the space of the configuration state function for complex atoms and ions. We also demonstrate how this method works for calculations of the energy structure and E1 transition properties of Fe XV ion.

Photoresponsive protamine ionic complex towards a smart hemostatic biomaterial

Protamine (PA) is the only licensed antidote for reversing heparin anticoagulation by electrostatically binding with heparin. Efforts have been made on designing various heparin-scavengers, while, it remains a great challenge for gaining the external-stimuli responsive PA-release material. In this study, a generic strategy is developed for fabricating photoresponsive protein materials with the designed azobenzene-containing surfactant. For the first time, based on the isomerization of azobenzene, both cationic and anionic proteins could be phase change biomaterials which are capable of transiting to isotropic state under UV irradiation at room temperature. The formation of isotropic state could set the proteins free from the binding state, activating their intrinsic biological functions. Employing this mechanism, one smart PA material for inhibiting heparin is developed, which could effectively photo-modulate the heparin concentration by turning on-and-off the free state of PA from the binding state. With good biocompatibility, the PA material addresses photoresponsive hemostatic activity in biological studies, confirming its great potential clinical values. This work provides a new designing strategy for gaining photocontrollable hemostasis materials, also opening new opportunities for developing photoresponsive protein drugs and biomedical materials.

Ultrasmall Metal TPZ Complexes with Deep Tumor Penetration for Enhancing Radiofrequency Ablation Therapy and Inducing Antitumor Immune Responses.

Radiofrequency ablation (RFA) is one of the most common minimally invasive techniques for the treatment of solid tumors, but residual malignant tissues or small satellite lesions after insufficient RFA (iRFA) are difficult to remove, often leading to metastasis and recurrence. Here, Fe-TPZ nanoparticles are designed by metal ion and (TPZ) ligand complexation for synergistic enhancement of RFA residual tumor therapy. Fe-TPZ nanoparticles are cleaved in the acidic microenvironment of the tumor to generate Fe2+ and TPZ. TPZ, an anoxia-dependent drug, is activated in residual tumors and generates free radicals to cause tumor cell death. Elevated Fe2+ undergoes a redox reaction with glutathione (GSH), inducing a strong Fenton effect and promoting the production of the highly toxic hydroxyl radical (•OH). In addition, the ROS/GSH imbalance induced by this treatment promotes immunogenic cell death (ICD), which triggers the release of damage-associated molecular patterns, macrophage polarization, and lymphocyte infiltration, thus triggering a systemic antitumor immune response and noteworthy prevention of tumor metastasis. Overall, this integrated treatment program driven by multiple microenvironment-dependent pathways overcomes the limitations of the RFA monotherapy approach and thus improves tumor prognosis. Furthermore, these findings aim to provide new research ideas for regulating the tumor immune microenvironment.

Adsorption of silver ions onto chitosan hydrogel: Structural studies

Chitosan indicate a significant potential in the field of water treatment due to polymer high porosity, large specific surface area and its ability to bind strongly heavy metal ions form aqueous solutions. Therefore, chitosan based hydrogels have been fabricated by physical crosslinking of the polymer chains via sol–gel method using sodium β-glycerophosphate (β-GP) for silver ions (Ag) removal from water solutions. The aim of this study was to provide experimental studies under batch conditions to perform adsorption isotherm and evaluate the effect of silver adsorption onto chitosan hydrogel morphological and structural changes using SEM, XRD, FTIR and EDX analyses. Obtained results provides the data on the structural changes in the chitosan hydrogels under Ag adsorption process. The FTIR spectra confirmed that the C-NH2 and OH groups contribute to the formation of chitosan - silver ion complexes. The presence of adsorbed Ag in the samples < 0.8 gAgL−1 were evidenced by the characteristic peak at 2θ = 46.35°. Regarding to EDX analysis the adsorption efficiency toward Ag ions, rises with an increase in Ag initial concentration, resulting in L-type isotherm. The percentage removal of silver ions efficiency obtained 34 % for the highest Ag initial concentration (10 gAg L−1). SEM micrographs after Ag adsorption performed morphology as homogeneous porous network and reveals Ag present in the structure resulting from effective Ag adsorption. This study verified structural changes resulted from silver ions adsorption and confirmed the potential for thermosensitive chitosan hydrogels to applied as an adsorbent for water treatment applications.

Design, synthesis, and evaluation of some metal ion complexes of mannich base derived from 2-Mercaptobenzimidazole as potential antimicrobial agents

This study aims to prepare new compounds and investigate them spectroscopically and biologically against selected types of positive and negative bacteria and fungi to demonstrate their biological effectiveness. The prepared ligand combining formaldehyde, indole, sulfa benzamide, and 2-mercapto benzimidazole, a Mannich base ligand (L) was synthesized. The six metal ions including Cobalt (II), Nickel (II), Copper (II), Palladium (II), Platinum (IV), and gold (III) have interacted with the ligand and formed new complexes. Different spectroscopic methods, including C.H.N.S., FTIR, UV- Range visible, 1HNMR, 13CNMR, mass spectra, magnetic moment, and molar conductivity were used to suggest the new geometry of the complexes. The result from the infrared spectrum showed that the ligand behaves as tridentate with all prepared complexes. Conductivity analysis revealed the electrolytic nature of palladium, platinum, and gold ions complexes and non-electrolytes. The antibacterial activity of the compounds that were produced was tested using an agar-well diffusion procedure towards two strains of gram-positive as well as two strains of gram-negative bacteria and fungi (Staphylococcus, Streptococcus, Escherichia coli, Pseudomonas aeruginosa, and Candida albicans) respectively at 0.02M. The standard (∆Eo) and (∆Hfo) of ligand and six complexes were calculated using the program Hyper chem 8.0.7. The research established that complexes are more stable than ligands. Calculated HOMO and LUMO and vibration frequencies using (parametric method 3 (PM3)) to find out the active sites in the ligand showed that they can coordinate and note the extent to which the results of theoretical vibrational frequencies are close to the process when calculating the vibrational frequency of the active aggregates.

Preparation, Identification And Biological Activity Of Some Metals Complexes With A New Ligand (4-Nitro-N-((6-Oxo-6,9-Dihydro-1H-Purin-2-Yl)Carbamothioyl)Benzamid)

This study aimed to synthesize and characterize a novel guanine derivative, namely ( 4-nitro-N-((6-oxo-6,9-dihydro-1H-purin-2-yl)carbamothioyl)benzamid) (abbreviated as NPBL4). This compound possesses an intriguing chemical structure, consisting of a guanine moiety (a bicyclic heterocyclic base) linked to a benzamide group through a carbamothioyl linker. The synthesis of this nitrogenous base derivative involved two steps. Firstly 4-nitro-N-thioformylbenzamide was synthesized by reacting 4-nitrobenzoyl chloride with ammonium thiocyanate in acetone. Subsequently, the obtained 4-nitro-N-thioformylbenzamide was reacted with guanine to yield the desired ligand. In addition to the ligand synthesis, the study focused on preparing complexes of various metal ions (Mn+2, Co+2, Ni+2, Cu+2, Zn+2, Cd+2, and Pd+2) with the prepared guanine derivative. The ligand and complexes were subjected to comprehensive characterization using techniques such as infrared spectra, ultraviolet-visible spectra, 1H-NMR, 13C-NMR spectra, elemental analysis (C.H.N.S.), molar conductivity measurement, magnetic susceptibility, atomic absorption, melting point determination, and study the biological activity for the complexes. The results of these characterization studies led to the determination of the general formulas for the prepared complexes, which were found to be [MCl2(NPB)2], where M represents the respective metal ion (Mn+2, Co+2, Ni+2, Cu+2, Zn+2, Cd+2, and Pd+2). Notably, the geometric shape of all the prepared complexes was determined to be an octahedron. In summary, this study successfully synthesized and characterized a novel guanine derivative (NPB) and investigated its complexes with various metal ions. The findings provided valuable insights into the chemical properties and structural features of these compounds.

Investigation of solution behavior of Differential Equations by Sumudu methods of random complex Partial Differential Equations

In this study, solutions of random complex partial differential equations were found using the two-dimensional Sumudu transformation method(STM). The initial conditions of a deterministic equation or the non-homogeneous part of the equation are transformed into random variables to obtain a random complex partial differential equation. With the help of the properties of two-dimensional Sumudu and inverse Sumudu transformation, an approximate analytical solution of a complex partial differential equation with random constant coefficients was obtained by selecting a random variable with an initial condition of Normal and Gamma distribution. The probability characteristics of the resulting solutions, such as expected value and variance, were obtained and graphically shown with the help of the Maple package program.

Tailored proton conductive membranes of PVdF-co-HFP: Investigating the synergistic effects of ammonium tetrafluoroborate and phosphoric acid dopants on dielectric characteristics

This study investigates the structural, thermal, and dielectric properties of pure PVdF-co-HFP matrix and its composite electrolytes, PVdF-co-HFP/NH4BF4[x], both before and after PA doping, using FTIR, SEM, TGA, and dielectric analyses. FTIR spectra reveal characteristic vibrational bands, confirming the presence of various functional groups and phases. SEM images display a smooth and homogeneous surface morphology for pure PVdF-co-HFP, while the composite electrolytes exhibit irregular dispersion of NH4BF4 salt and rougher surfaces upon PA doping. TGA analysis shows that the onset of thermal degradation occurs at approximately 370 ℃ for pure PVdF-co-HFP, while PA-doped samples demonstrate higher decomposition temperatures, exceeding 400 ℃ due to hydrogen bonding and ionic complex formation. The presence of NH4BF4 and PA doping also affects the crystallinity of the PVdF-co-HFP matrix, notably shifting the transition temperatures of the alpha and beta phases. Ionic conductivity measurements indicate that PA doping significantly enhances conductivity by increasing charge carrier concentration and facilitating ion transport. PA-doped PVdF-co-HFP/NH4BF4[10] showed the highest conductivity reaching 1.68 × 10−3 S.cm−1 at 1 MHz and 400 K. Dielectric studies reveal frequency-dependent behavior, with dielectric constant (ε') and loss (ε") showing distinct trends influenced by salt concentration and PA doping. The dielectric tangent loss (tanδ) of PA-doped PVdF-co-HFP/NH4BF4 composite membranes exhibits frequency and temperature dependence. At higher temperatures, tanδ increases with frequency, showing a resonance peak that shifts towards higher frequencies. The study elucidates the impact of PA doping on the structural, thermal, and electrochemical performance of PVdF-co-HFP/NH4BF4 composites, providing insights for their potential applications in advanced electrolyte systems.

Inaccuracy principle and dissolution mechanism of lithium iron phosphate for selective lithium extraction from brines

The electrochemical lithiation/delithiation (ELD) method with the typical active materials being LiFePO4 and LiMn2O4, is the next generation technique for the selective lithium extraction from slat-lake brines owning to the advantages of high selectivity and excellent capacity and feasibility. However, the dissolution of LiFePO4/FePO4 (LFP/FP) during the ELD is seldom studied and an inaccurate measurement method for dissolution may result in obtaining an incorrect feasible application range for LFP/FP. Here, electrochemical workstation-electrochemical quartz crystal microbalance (EW-EQCM) is first utilized in the brine system to acquire the in-situ dissolution behavior of LFP/FP redox couple and verify the inaccuracy principle of the dissolution measurement. Both experimental results and thermodynamic calculations demonstrated that the accurate dissolution ratios can only be obtained by iron ions and phosphates at pH < 2.7 and pH < 5.3, respectively, which is induced by the narrow soluble range of iron ions and the formation of Ca5(PO4)3OH and Mg3(PO4)2 precipitation. In addition, the stable pH range of LFP and FP is 4 to 10 and 3 to 5, respectively, and the dissolution is caused by the formation of thermodynamically more stable metal ions, metal ion complexes, and metal ion hydroxides. At the optimum pH, the capacity can maintain 35 mg/g with average dissolution ratios of the cathode and anode lower than 0.1 %. This research sheds light on the accurate dissolution measurement range and method, dissolution mechanism and feasible application range of the LFP/FP redox couple.

Elucidation of DNA binding properties of transition metal ion complexes of curcumin: An In Vitro study

Introduction: The present work aims to synthesize, characterize, and DNA binding properties of copper, nickel, zinc, and iron complexes of a well-known polyphenol drug curcumin. The metal ion complexes of curcumin's synthesized transition metal ion complexes were characterized by UV-vis spectroscopy and FTIR. Method: The complexation of curcumin with transition metal ion complexes changes the color of the curcumin based on the metal incorporated. Moreover, the shift in the absorption maxima of curcumin metal ion complexes may confirm the formation of coordination complexes. Then, FTIR results indicated that the coordination of curcumin with metal ions in the ketone group of curcumin confirms the formation of 1:2 (M: L) complexes. Results: Then, we evaluated the DNA binding properties of synthesized metal ion complexes of curcumin using electronic absorption spectra and agarose gel electrophoresis. The results indicated that the curcumin zinc complex exhibited less DNA binding constant among the four metal ion complexes than all the other compounds tested, confirming its weak interaction. Conclusion: Moreover, all the compounds degrade plasmid DNA, confirming their DNA cleavage activity. From our findings, these compounds will pave the way for developing new anticancer drugs with less toxicity.

Chemically Reversible Translational Moiré Superlattice Formations in the Two-Dimensional Films of the Zinc Phthalate Complex.

The exciting electronic properties of two-dimensional layered materials introduced by twist angle and lattice mismatch between two consecutive layers are well-recognized. The major challenge lies in the control over the moiré periodicity. Herein, we report a chemically directed way to achieve the desired precision over moiré periodicity of the assembly of a complex of zinc ions and o-phthalic acid utilizing soft bonds. The reaction of o-phthalic acid with zinc ions in the aqueous medium at 80 °C for 1 h followed by preserving the reaction mixture at ambient temperature (35 °C) resulted in translational moiré superlattices with precise periods. Those lattices are further stacked angularly to give rotational super-moiré lattices. Further, the role of the π-zinc ion interaction in the origin of moiré fringes was examined with the reaction with 8-hydroxyquinoline-5-sulfonic acid (HQS) that also established the reversible nature of the superlattices. The present observations also suggest the formation of moiré superlattice through ion insertion in a chemical lattice.

Preparation and Biochemical Activity of Copper-Coated Cellulose Nonwoven Fabric via Magnetron Sputtering and Alginate-Calcium Ion Complexation.

Alginate-based materials have gained significant recognition in the medical industry due to their favorable biochemical properties. As a continuation of our previous studies, we have introduced a new composite consisting of cellulose nonwoven fabric charged with a metallic copper core (CNW-Cu0) covered with a calcium alginate (ALG-Ca2+) layer. The preparation process for these materials involved three main steps: coating the cellulose nonwoven fabric with copper via magnetron sputtering (CNW → CNW-Cu0), subsequent deposition with sodium alginate (CNW-Cu0 → CNW-Cu0/ALG-Na+), followed by cross-linking the alginate chains with calcium ions (CNW-Cu0/ALG-Na+ → CNW-Cu0/ALG-Ca2+). The primary objective of the work was to supply these composites with such biological attributes as antibacterial and hemostatic activity. Namely, equipping the antibacterial materials (copper action on representative Gram-positive and Gram-negative bacteria and fungal strains) with induction of blood plasma clotting processes (activated partial thromboplastin time (aPTT) and prothrombin time (PT)). We determined the effect of CNW-Cu0/ALG-Ca2+ materials on the viability of Peripheral blood mononuclear (PBM) cells. Moreover, we studied the interactions of CNW-Cu0/ALG-Ca2+ materials with DNA using the relaxation plasmid assay. However, results showed CNW-Cu0/ALG-Ca2+'s cytotoxic properties against PBM cells in a time-dependent manner. Furthermore, the CNW-Cu0/ALG-Ca2+ composite exhibited the potential to interact directly with DNA. The results demonstrated that the CNW-Cu0/ALG-Ca2+ composites synthesized show promising potential for wound dressing applications.

Enhancing electrochromic performance and stability: A novel ionic complex based on carbon dots

Electrolytes are crucial in electrochemical applications such as rechargeable batteries, supercapacitors, fuel cells, and electrochromic devices (ECDs). Therefore, developing new electrolytes with high ionic conductivity, electrochemical stability, and environmental friendliness is essential for advancing next-generation electrochemical systems. Herein, we developed a novel type of ionic complexes composed of multivalent carbon dot polyanions (C dot) and equivalent alkali cations such as Li+ (Li-C dot), Na+ (Na-C dot), and K+ (K-C dot). As an electrolyte, the K-C dot demonstrated superior electrochromic behavior of Prussian blue (PB)–a promising electrochromic material for ECDs–compared to commercially available KCl. The PB thin films exhibit high coloration efficiency (η) of 103.5 cm2 C−1, good optical density (OD) of 0.90, and fast color switching time (1.5 and 2.6 s for the bleaching and coloring processes, respectively). Furthermore, the PB thin films exhibit long-term stability, retaining 97 % of the initial optical contrast (ΔT) even after 1,000 color switching cycles. The electrochromic performance of PB is influenced by counter cations such as Li+, Na+, and K+, which occupy the interstitial cavities in the lattice of PB during the electrochromic process. These results suggest that to improve the electrochromic performance of PB thin films in ECDs, it is essential to balance the migration of counter cations into and out of the lattice channels of the PB structure with the electron transfer between the PB thin film and the electrode substrate to maintain the charge neutrality of PB. We anticipate that our study will enhance the understanding of the electrochromic process in ECDs and provide new insights into the design of electrolytes for electrochemical systems.

Henkel‐like Decarboxylation Produces Mononuclear Arylalkalis, [4‐(CH3)3N(C6H4)M]+ which Hydrolyse and Undergo Surprising SN2 Reactions Between Alkali Hydroxides and (CH3)3NC6H5+

AbstractBenzoate substituted with a cationic quaternary ammonium group at the para‐position, [4‐(CH3)3N(C6H4)CO2], forms mononuclear alkali metal ion complexes, [4‐(CH3)3N(C6H4)CO2M]+ (M=Li, Na, K, Rb and Cs), which are observed by electrospray‐ionisation mass spectrometry. When mass selected and subjected to collision‐induced dissociation each of these complexes undergoes decarboxylation to produce the mononuclear arylalkali complex cations, [4‐(CH3)3N(C6H4)M]+, which subsequently react with water via hydrolysis to yield the quaternary ammonium cation, (CH3)3NC6H5+. The unexpected product ions, [M((CH3)2NC6H5)]+, [M(CH3OH)]+, and M+, which are associated with the hydrolysis pathway, suggest an unusual reaction occurring within the exit channel ion‐molecule complex, [(CH3)3NC6H5+MOH]+. DFT calculations were used to examine the: decarboxylation reaction of [4‐(CH3)3N(C6H4)CO2M]+, which readily proceeds via a four‐centred transition state; the hydrolysis and SN2 reactions accounting for formation of products in the exit channel, which are connected via a roaming mechanism in which the metal hydroxide moiety migrates from the para‐hydrogen of (CH3)3NC6H5+ to one of the methyl groups.

A multifunctional leather composite with good antibacterial and hygrothermal management capabilities

If not removed in a timely manner, the large amount of sweat produced by overheated human skin can cause thermal discomfort and health problems. Development of fabrics with cooling and dehumidifying capabilities is advantageous to improving the quality of human life. In this work, a natural leather-based Zn-monoethanolamine@lignin (Zn-MEA@lignin-leather) composite fabric with personal hygrothermal management properties was fabricated by infiltrating the permeable 3D network microstructure of the natural leather collagen fiber bundles with adhering moisture-absorbent hydrogel containing photothermal lignin. Due to the efficiency of the composite hydrogel in trapping water molecules, the fabric can promote evaporation of sweat from overheated skin surfaces. Compared to the conventional textiles, the composite leather fabric can reduce the humidity of simulated skin surface by about 40 % and accelerate the evaporation of sweat from the skin surface to promote reduction in temperature of the overheated body. Thanks to the good photothermal conversion efficiency of lignin, the hydrated composite fabric exhibits a favorable evaporation regeneration rate (0.498 kg m−2 h−1). In addition, the presence of zinc ions in the coordination complex imparts good antimicrobial efficiency to the composite fabric, with inactivation rates approaching 99.99 % for both Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli). Thus, the composite leather fabric holds great promise to personal hygrothermal management and healthcare.

A novel chitosan-based hydrogel microspheres for efficient heavy metal-ion adsorption

Pb (II) and Cu (II) are the most critical metal ion pollutants commonly found in wastewater, and prolonged exposure to these metal ions can pose serious risks to human health. Therefore, the removal of these pollutants from wastewater is of particular importance. In this study, soy hull nanocellulose/sodium alginate/chitosan (SHNC/SA/CS) hydrogel microspheres were prepared using the ion crosslinking method, and they were used to adsorb Pb (II) and Cu (II) present in wastewater. The SHNC/SA/CS hydrogel microspheres exhibited excellent toughness (18.67 MPa) and hydrophilicity (21.43° ± 0.65°), which improved their reuse rate. Furthermore, hydroxyl, carboxyl and amino groups served as excellent chelating groups and considerably improved the adsorption efficiency of the SHNC/SA/CS hydrogel microspheres. The SHNC/SA/CS hydrogel microspheres exhibited an ultrahigh adsorption rate and an outstanding adsorption capacity for Pb (II) and Cu (II), with an equilibrium adsorption period of 50 min. The equilibrium adsorption capacities for Pb (II) and Cu (II) reached 116.62 and 94.32 mg/g, respectively. Furthermore, the SHNC/SA/CS hydrogel microspheres maintained a removal rate of up to 80 % for Pb (II) and Cu (II) after 10 adsorption–desorption cycles, demonstrating their potential for reuse. The SHNC/SA/CS hydrogel microspheres demonstrated an adsorption performance superior to that reported for CS-based adsorption materials. Moreover, X-ray photoelectron spectroscopy revealed that the adsorption mechanisms of SHNC/SA/CS hydrogel microspheres for Pb (II) and Cu (II) included ion exchange, pore filling, complexation and electrostatic attraction. Moreover, a synergistic coordination effect existed between carboxyl and amino groups.

Experimental study on Na+ conductivity in NaAlBr4 and atomic-scale investigation of Na+ conduction

AbstractThe ionic conduction properties of Li/Na metal halides have been extensively studied, with recent attention turning towards Al-based systems. However, limited studies have focused on alkali Al bromides. In this study, we explored the Na+ conduction properties of NaAlBr4. Conductivity measurements at 30 °C revealed a Na+ conductivity of 1.2 × 10−5 S/cm, surpassing that of isostructural NaAlCl4 threefold. Molecular dynamics (MD) simulations to elucidate the conduction mechanisms revealed that Na+ conduction was not observed in stoichiometric NaAlBr4, which has high formation energies of Na+ vacancies and interstitials (0.88 eV and 0.73 eV, respectively). Nevertheless, a conductivity of 1.2 × 10−5 S/cm was observed. The activation energy for ion conduction was experimentally determined as 0.43 eV, and the migration energies were calculated as 0.26 eV (Na+ vacancies) and 0.16 eV (Na+ interstitials) by MD simulations. These discrepancies in ion conduction were partially explained by the role of transient defects enriched via ball milling in facilitating Na+ conduction on the particle surface, offering insights into the complex ion conduction of ball-milled NaAlBr4.

Synthesis, diagnosis as well as Biological activity studies of some metal ion complexes of Schiff Bases Derived from 4-aminoantipyrine

قواعد شيف متعددة السن ذوات الصيغة L1= اورثو هايدروكسي انيلين -٤ - امینو انتبيرين N',N) بنزیلیدین) تم تحضيرها من تكثيف البنزايل و٤-امينو انتيبرين مع ۲-امينو فينول -۲،۱ امينو ٤ كلورو فينول بنسبة مولية (١:١:١) لكل مكون . واستخدمت هذه الليكاندات لتحضير المعقدات ذوات الصيغة [ML1 Cl]Cl و [ML2]Cl2 حيث ان Zn(II) M= Mn(II), Co(II), Ni(II),. تم استخدام التقنيات التالية لتشخيص الليكاندات والمعقدات: مطيافية الاشعة فوق البنفسجية والاشعة تحت الحمراء - المرئية وطيف الرنين النووي المغناطيسي للبروتون 1HNMR والتحليل الدقيق لايونات العناصر والكاربون والهيدروجين والنتروجين بالاضافة الى التوصيلية الكهربائية المولارية وقياسات الحساسية المغناطيسية. دلت القياسات التي تم الحصول عليها من التوصيلية الكهربائية المولارية والتي تم اجراؤها بمحلول DMSO ان جميع معقدات (L1) كانت الكتروليتية بنسبة (١:١) بينما معقدات (L2) كانت الكتروليتية بنسبة (1:2). كما اظهرت نتائج القياسات المستخدمة في هذه الدراسة ان مواقع التناسق لليكاند (L1) مع الأيون المركزي كانت من خلال ذرة الاوكسجين الفينولية وذرتين نيتروجين لمجموعتي الازوميثين اما بالنسبة لـ (L2)فبالاضافة للذرات المانحة المذكورة سابقا يتم التناسق مع ذرة الاوكسجين لمجموعة الكاربونيل الطرفية. جميع المعقدات اظهرت التناسق الرباعي بشكل هندسي رباعي السطوح ايضا تمت دراسة الفعالية البايولوجية للمركبات المحضرة ضد البكتريا موجبة الكرام (+)Staphylococcus aurous وسالبة الكرام (-) Klebsiella pneumonia.