Metal Cations Research Articles

Strengthening cationic repulsion on graphene oxide membrane to boost water desalination

BackgroundAs a hydrophilic two-dimensional material with oxygen-containing groups on its basal planes, graphene oxide (GO) has been used for the fabrication of GO-based membranes to purify/desalinate water. However, promoting salt rejection of GO-based membranes is challenging while maintaining high water permeability. MethodsFirst, the mercaptoethylamine-modified Ag NWs (Ag-MA) were prepared by mixing Ag NWs and MA to form Ag—S bonds. Then, Ag-MA was deposited on the GO membrane under externally assisted filtration to achieve the GO/Ag-MA membrane, which ensures the well-stacking of GO sheets and the even coating of GO membrane. Therefore, the delicately fabricated membrane possesses great electropositive cations and high swelling-tolerance in water solution. Significant findingsWe found that a high electrostatic repulsive interaction between the amino group and metal cations in GO/Ag-MA membrane aided the promotion of rejection rates, which was up to 75 % for both K+ and Mg2+, surpassing that of the previously reported values. This work highlights a new approach for enhancing the electrostatic repulsion with metal cations near the surface/interface of GO-based membranes and their application in the development of water desalination and purification.

Removal of heavy metal ions (Pb2+, Cu2+, Cr3+, and Cd2+) from multimetal simulated wastewater using 3-aminopropyl triethoxysilane grafted agar porous cryogel

In this study, we have developed agar, a seaweed derived polysaccharide based green adsorbent for the removal of heavy metal ions (Pb2+, Cu2+, Cr3+ and Cd2+) from multimetal solution. Porous cryogels of agar grafted with 3-aminopropyl triethoxysilane (APTES) were prepared by freeze-drying. The adsorption capacity and selectivity of the optimized APTES-agar cryogel for heavy metal ions (Cu2+, Cr3+, Pb2+, Cd2+) were investigated in multimetal solutions. >95 % of all the cationic metal ions were removed from 400 mg/L multimetal metal solutions having equal concentrations of each metal at pH 5.5. The experimental adsorption capacities of Cr3+, Cu2+, Pb2+, and, Cd2+ were changed from 39.14, 39.0, 39.20, 37.93 mg/g, to 52.58, 52.70, 45.53, 31.10 mg/g, respectively, for the 400 mg/L and 800 mg/L multimetal solutions suggesting competitive adsorption of the metal ions for active sites. The competitive adsorption studies showed that Cd ions had lower affinity than other metal ions for active sites on APTES grafted agar surface, and adsorption followed in the order of Cu2+ ≈ Cr3+ > Pb2+ > Cd2+. The developed seaweed-derived agar-based porous adsorbent exhibits promise in the removal of several heavy metal ions from wastewater, and this approach would increase the use of natural polysaccharides that are sustainable.

Removal of heavy metals from aqueous solutions by adsorption on zeolites synthesized from aluminum saline slags

Three heavy metals (Cu2+, Cd2+ and Pb2+) were removed from aqueous solutions using zeolites prepared from saline slags, a very important waste generated during aluminum recycling. Zeolites were characterized by powder X-ray diffraction, thermal analysis, Fourier transform infrared spectroscopy, X-ray microfluorescence, element chemical analysis, nitrogen adsorption at −196 °C and electron microscopy. The textural and structural properties of X-type faujasite zeolite convert it in a promising adsorbent in aqueous streams. Removal of the heavy metals was evaluated in batch mode, studying the adsorbent dose, the initial concentration of the heavy metal, the selectivity of the solid in case of mixtures with various metal cations and the recyclability of the solid. The kinetic and equilibrium results were evaluated using both pseudo-first- and pseudo-second-order kinetics, and Langmuir, Freundlich and Toth equation isotherms for the equilibrium. The time needed to reach equilibrium was between 10 and 20 min. Faujasite was highly effective in removing Cu2+, Cd2+ and Pb2+ from aqueous solutions, much higher than analcime and pollucite, other two zeolites recently synthesized by us from aluminum slags, and used in this work for comparison purposes. The maximum adsorption capacity was 591 mg/g for Pb2+, 304 mg/g for Cu2+ and 279 mg/g for Cd2+.

Melanin in the Retinal Epithelium and Magnetic Sensing: A Review of Current Studies.

Coming in a variety of forms, melanin is one of the most abundant, stable, diverse, and evolutionarily ancient pigments found in living things in nature. These pigments often serve protective functions, typically well-adapted to their specific roles. One such protective function is metal chelation and cation exchange, which help regulate and buffer metal concentrations within cells. By binding to certain metals, melanin can acquire magnetic properties. Because of this, it may play a role in magnetic effects and possibly in the response of organisms to external magnetic fields and magnetic sensing. While there is melanin in plants, microbes, fungi, and invertebrates, certain types of melanin are specifically associated with the retina in vertebrates, including migrating bird and fish species. In this review, we examine studies focusing on the properties of melanin in these parts of the body and their possible association with magnetic sensing, and generally, magnetic sensing in the retina.

Influence of Pseudomonas aeruginosa-based biopolymer on mitigating soil erosion and heavy metal dispersion

Extreme weather phenomena caused by climate change have exacerbated soil erosion and the subsequent dispersion of pollutants. Pseudomonas aeruginosa is known to contribute to the remediation of polluted water and reduce the geochemical mobility of heavy metals in contaminated soil. However, studies on the influence of biopolymers produced by soil microbes and P. aeruginosa on physical soil properties and soil erosion are limited. We aimed to investigate the influence of soil microbes on the mitigation of soil erosion and geochemical dispersion of heavy metals using a naturally occurring microbial substance, P. aeruginosa-based biopolymer (PBB). The PBB comprised carboxyl, hydroxyl, and amine surface functional groups; consequently, the biopolymer effectively sequestered Cd (maximum sorption capacity qm = 45.7 mg/g), Cu (qm = 26.7 mg/g), Pb (qm = 64.9 mg/g), and Zn (qm = 26.1 mg/g) in the solution. The PBB amendment of the soil improved the physical properties associated with soil erosion, increasing soil aggregation stability and shear strength by 41.6 % and 36.8 %, respectively. The extraction of heavy metals from soil via synthetic precipitate leaching decreased by 54.2 % following the PBB amendment, and a negative correlation was observed between soil aggregate stability and heavy metal extraction, indicating that this microbial substance could immobilize pollutants by adsorbing cationic metal ions and inhibiting water-induced disaggregation. In the soil erosion experiments, soil loss and heavy metal extraction decreased by 70.9 % and 43.8 %, respectively, following the PBB amendment. These aggregation and sorption effects of the PBB underscore the potential of soil microbes to mitigate soil erosion and immobilize the geochemical dispersion of heavy metals, thereby contributing to the conservation of soil and water quality in areas surrounding contaminated slopes and heavy metal-contaminated areas, such as cut slopes, agricultural fields, mine dumps, and dams.

The Heteropolyacid-Catalyzed Conversion of Biomass Saccharides into High-Added-Value Products and Biofuels

The industrial processes used to produce paper and cellulose generate many lignocellulosic residues. These residues are usually burned to produce heat to supply the energy demands of other processes, increasing greenhouse gas emissions and resulting in a high environmental impact. Instead of burning these lignocellulosic residues, they can be converted into saccharides, which are feedstock for high-value products and biofuels. Keggin heteropolyacids are efficient catalysts for obtaining saccharides from cellulose and hemicellulose and converting them into bioproducts or biofuel. Furfural, 5-hydroxymethylfurfural, levulinic acid, and alkyl levulinates are important platform molecules obtained from saccharides and raw materials in the biorefinery processes used to produce fine chemicals and biofuels. This review discusses the significant progress achieved in the development of the processes based on heteropolyacid-catalyzed reactions to convert biomass and their residues into furfural, 5-hydroxymethylfurfural, levulinic acid, and alkyl levulinates in homogeneous and heterogeneous reaction conditions. The different modifications that can be performed to a Keggin HPA structure, such as the replacement of the central atom (P or Si) with B or Al, the doping of the heteropolyanion with metal cations, and a proton exchange with metal or organic cations, as well as their impact on the catalytic activity of HPAs, are detailed and discussed herein.

Metal-Exchanged Phosphomolybdic Acid Salts-Catalyzed Esterification of Levulinic Acid

We examined the effectiveness of metal-exchanged phosphomolybdic acid salts in converting levulinic acid, derived from biomass, into valuable products (alkyl levulinate). We prepared salts of phosphomolybdic acid using different metals (Fe3+, Al3+, Zn2+, Cu2+, Mn2+, Ni2+, and Co2+). The influence of metal cations on the conversion and selectivity of the reactions was assessed. We found that the salts prepared with iron and aluminum phosphomolybdate were the most effective catalysts for the esterification of levulinic acid with methanol, with the conversion and selectivity tending towards 100% after 6 h of reaction at a temperature of 323 K. The effect of catalyst loading and its recovery and reuse was evaluated; the results from the reaction using aluminum phosphomolybdate remained similar for four cycles of use. The influence of temperature on conversion and selectivity was investigated between 298 and 353 K. The reactivity of different alcohols with a carbon chain size of C1-C4 was assessed and conversions above 65% were obtained for all alcohols tested under the conditions evaluated, except for tert-butyl alcohol. These catalysts are a promising alternative to the traditional soluble and corrosive Brønsted acid catalysts. The superior performance of these catalysts was ascribed to the higher pH decline triggered by the hydrolysis of these metal cations.

Application of Hard and Soft Acid‐base Theory to Construct Heterometallic Materials with Metal‐oxo Clusters

AbstractHeterometallic cluster‐based materials offer the potential to incorporate multiple functionalities, leveraging the aggregation effects of clusters and translating this heterogeneity and complexity into unexpected properties that are more than just the sum of their components. However, the rational construction of heterometallic cluster‐based materials remains challenging due to the complexity of metal cation coordination and structural unpredictability. This minireview provides insights into a general synthetic strategy based on Hard and Soft Acids and Bases (HSAB) theory, summarizing its advantages in the designed synthesis of discrete heterometallic clusters (intracluster assembly) and infinite heterometallic cluster‐based materials (intercluster assembly). Furthermore, it emphasizes the potential to exploit the intrinsic properties of mixed components to achieve breakthroughs across a broad range of applications. The insights from this review are expected to drive the progress of heterometallic cluster‐based materials in a controllable and predictable manner.

Why is binding of a divalent metal cation to a structural motif containing four carboxylate residues not accompanied by a conformational change?

We earlier showed that Torpedo californica acetylcholinesterase (AChE) contains a cluster of four conserved aspartates that can strongly bind divalent cations, which we named the 4D motif. Binding of the divalent metal cations greatly increases its thermal stability. Here we systematically examined all available crystallographic structures of T. californica AChE. Two additional metal-binding sites were identified, both composed of acidic and histidine residues. Relative binding to the 4D and additional sites was studied using metadynamics simulations. It was observed that in crystal structures devoid of metal ions in the 4D site, the conformation of T. californica AChE is almost identical to that in structures in which it is occupied by a divalent metal ion. Closer examination of the 4D motif reveals that three of the four acidic residues form ion pairs with conserved basic residues surrounding them. We named this new motif the 4A/3B motif. Molecular dynamics with quantum potential simulations was used to quantify the 4D motif's binding strength compared with that of the metal-binding site in the protein fXIIIa, which consists of four aspartates, but is devoid of adjacent cationic residues. Whereas fXIIIa's 4D site, in the absence of a metal cation, expanded significantly in the simulation, that of Torpedo AChE displayed only minor periodic changes in size. Furthermore, the energy of metal ion unbinding from the two sites differs by ca. 10 kcal/mol. We identified several other proteins in the PDB that contain the 4A/3B motif, whose conformations are identical in the presence or absence of a metal ion. An animated Interactive 3D Complement (I3DC) is available in Proteopedia at https://proteopedia.org/w/Journal:Protein_Science:4.

Computational Evidence for Bisartan Arginine Blockers as Next-Generation Pan-Antiviral Therapeutics Targeting SARS-CoV-2, Influenza, and Respiratory Syncytial Viruses

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), influenza, and respiratory syncytial virus (RSV) are significant global health threats. The need for low-cost, easily synthesized oral drugs for rapid deployment during outbreaks is crucial. Broad-spectrum therapeutics, or pan-antivirals, are designed to target multiple viral pathogens simultaneously by focusing on shared molecular features, such as common metal cofactors or conserved residues in viral catalytic domains. This study introduces a new generation of potent sartans, known as bisartans, engineered in our laboratories with negative charges from carboxylate or tetrazolate groups. These anionic tetrazoles interact strongly with cationic arginine residues or metal cations (e.g., Zn2+) within viral and host target sites, including the SARS-CoV-2 ACE2 receptor, influenza H1N1 neuraminidases, and the RSV fusion protein. Using virtual ligand docking and molecular dynamics, we investigated how bisartans and their analogs bind to these viral receptors, potentially blocking infection through a pan-antiviral mechanism. Bisartan, ACC519TT, demonstrated stable and high-affinity docking to key catalytic domains of the SARS-CoV-2 NSP3, H1N1 neuraminidase, and RSV fusion protein, outperforming FDA-approved drugs like Paxlovid and oseltamivir. It also showed strong binding to the arginine-rich furin cleavage sites S1/S2 and S2′, suggesting interference with SARS-CoV-2’s spike protein cleavage. The results highlight the potential of tetrazole-based bisartans as promising candidates for developing broad-spectrum antiviral therapies.

Formamidinium Incorporates into Rb-based Non-Perovskite Phases in Solar Cell Formulations.

Organic-inorganic hybrid perovskite materials, such as formamidinium lead iodide (FAPbI3), are among the most promising emerging photovoltaic materials. However, the spontaneous phase transition from the photoactive perovskite phase to an inactive non-perovskite phase complicates the application of FAPbI3 in solar cells. To remedy this, alkali metal cations, most often Cs+, Rb+ or K+, are included during perovskite synthesis to stabilize the photoactive phase. The atomic-level mechanisms of stabilization are complex. While Cs+ dopes directly into the perovskite lattice, Rb+ does not, but instead forms an additional non-perovskite phase, and the mechanism by which Rb confers increased stability remains unclear. Here, we use 1H-87Rb double resonance NMR experiments to show that FA+ incorporates into the Rb-based non-perovskite phases (FAyRb1-yPb2Br5 and δ-FAyRb1-yPbI3) for both bromide and iodide perovskite formulations. This is demonstrated by changes in the 1H and 87Rb chemical shifts, 1H-87Rb heteronuclear correlation spectra, and 87Rb{1H} REDOR spectra. Simulation of the REDOR dephasing curves suggests up to ~60 % FA+ incorporation into the inorganic Rb-based phase for the bromide system. In light of these results, we hypothesize that the substitution of FA+ into the non-perovskite phase may contribute to the greater stability conferred by Rb salts in the synthesis of FA-based perovskites.

Formamidinium Incorporates into Rb‐based Non‐Perovskite Phases in Solar Cell Formulations

AbstractOrganic‐inorganic hybrid perovskite materials, such as formamidinium lead iodide (FAPbI3), are among the most promising emerging photovoltaic materials. However, the spontaneous phase transition from the photoactive perovskite phase to an inactive non‐perovskite phase complicates the application of FAPbI3 in solar cells. To remedy this, alkali metal cations, most often Cs+, Rb+ or K+, are included during perovskite synthesis to stabilize the photoactive phase. The atomic‐level mechanisms of stabilization are complex. While Cs+ dopes directly into the perovskite lattice, Rb+ does not, but instead forms an additional non‐perovskite phase, and the mechanism by which Rb confers increased stability remains unclear. Here, we use 1H−87Rb double resonance NMR experiments to show that FA+ incorporates into the Rb‐based non‐perovskite phases (FAyRb1‐yPb2Br5 and δ‐FAyRb1‐yPbI3) for both bromide and iodide perovskite formulations. This is demonstrated by changes in the 1H and 87Rb chemical shifts, 1H−87Rb heteronuclear correlation spectra, and 87Rb{1H} REDOR spectra. Simulation of the REDOR dephasing curves suggests up to ~60 % FA+ incorporation into the inorganic Rb‐based phase for the bromide system. In light of these results, we hypothesize that the substitution of FA+ into the non‐perovskite phase may contribute to the greater stability conferred by Rb salts in the synthesis of FA‐based perovskites.

Synergistic Regulation of DNA Morphology by Metal Cations and Low pH.

As a flexible biomolecule, the spatial structure of DNA is variable. The effects of concentration, metal cations, and low pH on DNA morphology were studied. For the high concentration of DNA, the cross-linked branch-like or network structures were formed. For the low concentration of DNA, isolated, random and freely loose linear DNA chains were presented. These phenomena were related to the intermolecular interactions. Branch-like DNA structures were reformed with the addition of metal cations to the low concentration of DNA at pH 7-4, suggesting the negative charges of DNA were neutralized, thus transforming the spatial structure of DNA into a low charge density morphology and presenting the hypochromic effect. Compared to the monovalent alkaline metal cations, more negative charges of DNA were screened by the alkaline-earth metal cations. Distinct DNA morphologies were observed for pH 3. The linear and condensed DNA structures were simultaneously observed, which was met regardless of the solution with or without the addition of metal cations. This was further confirmed by the absorbance of DNA. Compared to the pure DNA, bulky and aggregated DNA collapsed structures were formed when the sodium and magnesium cations were added to the reaction solution. In addition, it was verified that the condensed DNA structures failed to revert back to the chain structure by neutralizing acidic solutions with alkali, but the compacted DNA spheres became loose. The conductivities of various DNA morphologies were measured. They were morphology-dependent. This study provides guidance forthe behavior of DNA in the acidic solutions and further promotes the application of DNA in DNA-based nano-optoelectronic devices.

Effects of copper and lead on the sorption and desorption behaviors of benzene onto humic acids and black carbons

ABSTRACT Due to rapid urbanization and industrialization, combined pollution caused by BTEX (benzene, toluene, ethylbenzene, and xylene) and heavy metals has become ubiquitous in soils, which would pose serious health risks to humans. However, the effects of heavy metals on the sorption and desorption behaviors of BTEX have not been fully elucidated. In this study, the effects of Cu2+ and Pb2+ ions on the sorption and desorption of benzene onto humic acids and black carbons were investigated. The results showed that Cu2+ and Pb2+ ions significantly reduced the sorption capacity, slowed down the sorption rate, and made the desorption less hysteretic of benzene on both humic acids and black carbons. Furthermore, the inhibitory effects by Pb2+ were significantly stronger than those of Cu2+. By combining the results of Fourier transform infrared spectroscopy and the site energy distribution model, it can be speculated that the hydration shells of Cu2+ and Pb2+ ions partially cover the surface of humic acids and black carbons, blocking their micropores and shielding sorption sites, consequently inhibiting the sorption of benzene. This study highlights that coexisting metal cations can significantly influence the fate of BTEX in soils.

The influence of metal cations on the dissolution and transformation of biotite

The influence of metal cations on the dissolution and transformation of biotite

Soil and plant cations as affected by application of wood ash, biochar, and papermill biosolids

AbstractRecycling woody biomass for application to croplands is one option to divert materials from landfills and simultaneously improve degraded soil properties. Considering the diversity of materials that vary widely in characteristics, an understanding of the comparative effects of a single or combined application of these byproducts is missing with regards to soil C accumulation and availability of base and metallic cations. A field study was conducted in Québec City, QC, Canada, to assess the effects relative to untreated control of wood ash (10 and 20 Mg dry wt. ha−1), pine biochar (10 Mg dry wt. ha−1), papermill biosolids (12 Mg PB dry wt. ha−1), and a combination of wood ash and PB on soil C, pH, and cations in a circumneutral loamy soil. The site was cropped to a corn (Zea mays L.)–soybean [Glycine max (L.) Merr.] rotation. All materials were applied before corn planting and the effects of treatment were followed over two growing seasons. Applying wood ash resulted in the statistically largest increases (p < 0.01) in soil pH, percentage base saturation, and Mehlich‐3 K, Ca, Mg, Zn, and Cd. Wood ash also increased K concentration in straw and total K accumulation for both plants, but its effect on plant metallic cations was limited. With a single application, PB only increased Mehlich‐3 Ca with no further effect when combined with wood ash, while pine biochar was limited to sequester soil C. Therefore, this study indicated that wood ash could benefit a corn–soybean rotation by enhancing soil quality and crop yield.

Sorption-desorption of rare earth metal cations by ferromanganese crusts of Govorov’s guyote of the Magellanic Mountains of the Pacific Ocean

The article presents the results of experimental studies on the sorption and desorption of rare earth metal (REM) cations by cobalt-rich ferromanganese crusts (CMC) of Govorov’s guyot. It has been established that the sorption of REM cations occurs on the ore minerals KMK – Fe-vernadite, vernadite, Mn-feroxygite, goethite. The crusts are characterized by a high exchange capacity – 1.78–3.57 mg-eq/g, which increases in a series: (Dy Gd Lu Sm Nd Y, La Eu) Ce. The sorption of REM cations proceeds by an ion exchange equivalent irreversible mechanism. The exchange complex of ore minerals consists of Na+, K+, Ca2+, Mg2+ cations, which contribute 97‒98% to their total capacity. The crusts are characterized by the group sorption of REM cations from multicomponent aqueous solutions of metal salts. The selectivity of ore manganese and ferruginous minerals of crusts to REM cations is significantly higher than to the main cations of ocean water. From experimental data on the desorption of sorbed REM cations with NaCl solution, their irreversible absorption by ore minerals follows, and the strengthening of the chemical bond of sorbed REM cations with the main structural elements of these minerals over time. An important property of ore minerals, primarily manganese minerals, is their chemical and structural stability in aqueous solutions of electrolytes. This suggests the repeated use of ferromanganese crusts as sorbents of REM cations.

Control of sensitivity in metal oxide electrolyte gated field-effect transistor-based glucose sensor by electronegativity modulation

In this study, the sensitivity of electrolyte-gated field-effect transistor-based glucose sensors using oxide semiconductor materials was controlled via electronegativity modulation. By controlling the enzymatic reaction between glucose and glucose oxidase, which is affected by the surface potential, the sensitivity of the glucose sensor can be effectively adjusted. To evaluate the sensitivity characteristics of the glucose sensor according to electronegativity control, devices were fabricated based on InO through Ga and Zn doping. The results confirmed that the specific sensitivity range could be adjusted by increasing the electronegativity. In addition, density functional theory calculations, confirmed that the attachment energy of the surface-functionalized material and the enzyme binding energy in the surface-functionalized thin film can be modulated depending on the electronegativity difference. The dissociation constant was controlled in both directions by doping with metal cations with larger(Ga, 1.81) or smaller(Zn, 1.65) electronegativities in InO(In, 1.78). We expect that this study will provide a simple method for the gradual and bidirectional control of the glucose sensitivity region.

Thermogenic Adipocytes Promote M2 Macrophage Polarization through CNNM4-Mediated Mg Secretion.

M2 macrophages promote adipose tissue thermogenesis which dissipates energy in the form of heat to combat obesity. However, the regulation of M2 macrophages by thermogenic adipocytes is unclear. Here, it is identified magnesium (Mg) as a thermogenic adipocyte-secreted factor to promote M2 macrophage polarization. Mg transporter Cyclin and CBS domain divalent metal cation transport mediator 4 (CNNM4) induced by ADRB3-PKA-CREB signaling in thermogenic adipocytes during cold exposure mediates Mg efflux and Mg in turn binds to the DFG motif in mTOR to facilitate mTORC2 activation and M2 polarization in macrophages. In obesity, downregulation of CNNM4 expression inhibits Mg secretion from thermogenic adipocytes, which leads to decreased M2 macrophage polarization and thermogenesis. As a result, CNNM4 overexpression in adipocytes or Mg supplementation in adipose tissue ameliorates obesity by promoting thermogenesis. Importantly, an Mg wire implantation (AMI) approach is introduced to achieve adipose tissue-specific long-term Mg supplement. AMI promotes M2 macrophage polarization and thermogenesis and ameliorates obesity in mice. Taken together, a reciprocal regulation of thermogenic adipocytes and M2 macrophages important for thermogenesis is identified, and AMI is offered as a promising strategy against obesity.

Structures and NMR Solution Dynamics of Diorganotin Complexes with Bulky Quadridentate Salen‐ and Salphen‐Type Schiff Bases (N2O2) Incorporating Diazenylpyridyl Side Arms

AbstractA series of six complexes [n‐Bu2Sn(L1)]⋅S (S=Benzene/toluene, mixed/partial) (1), [Ph2Sn(L1)]n⋅S (S=Benzene) (2), [Bz2Sn(L1)] (3), [n‐Bu2Sn(L2)]n (4), [Ph2Sn(L2)] (5) and [Bz2Sn(L2)] (6) were synthesized using diorganotin(IV) oxide precursors and two new bis‐Schiff bases containing N2O2 donor atoms. The Schiff bases, H2L1 and H2L2, were prepared by reacting ethane‐1,2‐diamine or benzene‐1,2‐diamine with 2‐hydroxy‐5‐(pyridin‐3‐yldiazenyl)benzaldehyde in absolute ethanol. Compounds 1–6 were characterized by IR and NMR spectroscopies, as well as by solid‐state single‐crystal X‐ray diffraction (except for 3 and 6). In all the complexes the bis‐Schiff bases occupy the equatorial positions and the R groups are in axial sites. However, while 1 and 5 are discrete molecules where the tin atoms adopt distorted octahedral geometries, 2 and 4 are monoperiodic polymers with the metal cations in pentagonal bipyramidal environments. Although solid state crystallographic results revealed asymmetrical molecular configurations, solution NMR studies proved symmetric arrangements for all the compounds. Tin NMR spectroscopy confirmed that all complexes are six‐coordinate in solution, despite variations in solid‐state coordination. Further analysis using Hirshfeld surface and fingerprint plots provided insights into intermolecular interactions in compounds 1, 2, 4, and 5. This comprehensive study underscores the structural diversity and solution‐state dynamics of organotin(IV) complexes synthesized using novel Schiff bases.