Complex Formation Research Articles

Tetrafunctionalized Azocalix[4]resorcinarene Dye: A Chromogenic Supramolecule Used for the Selective Liquid-Liquid Extraction and Spectrophotometric Determination of Cu(II)

Background: The detection and extraction of trace metal ions, particularly copper(II), are critical for environmental monitoring and industrial processes. Calixresorcinarene, with its unique cavity structure, offers excellent platforms for designing selective chemosensors and extractants. Functionalization of calixresorcinarene with azo groups can enhance their chromogenic properties, enabling both extraction and detection in a single step. Objective: This study aimed to evaluate its (Azocalix[4]resorcinaren) efficacy as a selective chemosensor for the liquid-liquid extraction and spectrophotometric determination of Cu(II) ions. Methods: Application in Extraction and Detection: The ability of the dye to selectively extract Cu(II) ions from aqueous solutions was investigated via liquid-liquid extraction experiments. The dye-Cu(II) complex formation was monitored by UV-Vis spectrophotometry, with systematic optimization of experimental conditions, including pH, solvent system, and extraction duration. Results: The synthesized azocalix[4]resorcinarene dye exhibited a pronounced selectivity towards Cu(II) ions, forming a stable, colored complex. The complexation induced a distinct bathochromic shift in the absorption spectrum, allowing for precise spectrophotometric detection. Optimal extraction was achieved at a specific pH and solvent combination, with the method demonstrating a low detection limit and high sensitivity. The dye showed minimal interference from other metal ions, confirming its selectivity for Cu(II). Conclusion: The tetrafunctionalized azocalix[4]resorcinarene dye is a highly effective chromogenic agent for the selective extraction and detection of Cu(II) ions. Its robust performance in both extraction efficiency and spectrophotometric detection underscores its potential utility in environmental analysis and industrial applications where trace metal detection is crucial.

Effect of glyceryl monopalmitate on the gelatinization, rheological and retrogradation properties of Japonica rice starch.

Starch-based food is easy to retrograde during cold storage after gelatinization, which leads to quality fission and a relatively short shelf life. Some lipids can effectively enhance the storage stability of starch gels by the formation of starch-lipid complexes. The present study aimed to investigate the effects of glyceryl monopalmitate (GMP) on gelatinization, rheological and retrogradation properties of Japonica rice starch (JS) at different conditions and to analyze the correlation between the physical-chemical properties and structural characteristics of the JS-GMP complex. The addition of GMP to JS could retard the process of starch gelatinization through forming JS-GMP complexes. The resulting JS-GMP pastes were typical pseudoplastic fluids with shear thinning, and their solid-like properties were prominent (tan δ < 1). In addition, the retrogradation of JS-GMP complex was more inhibited during storage at -18 than at 4 °C. The added amount of GMP was negatively and highly associated with the minimum viscosity, consistency coefficient, hardness and elasticity, whereas it was positively and highly correlated with the breakdown value, fluid characteristic index and relative crystallinity. The relative crystallinity of JS was affected by GMP in an approximate dose-dependent manner. The addition of GMP can influence the gelatinization properties, rheological properties and retrogradation characteristics of JS, and the formation of JS-GMP complex could improve the quality and storage stability of starch gel, which provides ideas for the quality control of starch-based food. © 2024 Society of Chemical Industry.

CD36 deficiency protects lipopolysaccharide-induced sepsis via inhibiting CerS6-mediated endoplasmic reticulum stress

The type 2 scavenger receptor CD36 functions not only as a long chain fatty acid transporter, but also as a pro-inflammatory mediator. Ceramide is the simple N-acylated form of sphingosine and exerts distinct biological activity depending on its acyl chain length. Six ceramide synthases (CerS) in mammals determine the chain length of ceramide species, and CerS6 mainly produces C16-ceramide. Endotoxin-induced septic shock shows high mortality, but the pathophysiologic role of sphingolipids involved in this process has been hardly investigated. This paper aims to highlight the different role of CerS isoforms in endotoxin-induced inflammatory responses and the regulatory role of CD36 in CerS6 protein degradation with an emphasis as the potential therapeutic candidates in humans. Lipopolysaccharide (LPS), the endotoxin of the Gram-negative bacterial cell wall, was treated to induce endotoxin-induced inflammation both in vitro and in vivo. CerS6-derived C16-ceramide propagated LPS-induced inflammatory responses activating various intracellular signaling pathways, such as mitogen-activated protein kinase and nuclear factor-κB, resulting in the formation of inflammasome complex and pro-inflammatory cytokines. Mechanistically, CerS6-derived C16-ceramide augmented inflammatory responses via endoplasmic reticulum stress, and CerS6 protein stability was regulated by CD36. Finally, CerS6 protein expression and LPS-induced lethality were strikingly reduced in CD36 knockout mice. Collectively, our findings show that CerS6-derived C16-ceramide plays a pivotal role in endotoxin-induced inflammation and suggest CerS6 and its regulator CD36 as possible targets for therapy under life-threatening inflammation such as septic shock.

N-doped silicon QDs: facile synthesis and application as sensor for discrimination and selective detection of oxytetracycline, tetracycline, and chlortetracycline in foods.

Nitrogen-doped silicon quantum dots (N-SiQDs) with a quantum yield of up to 37.8% were simply synthesized using inexpensive and readily available silica as the silicon source. Based on the internal filter effect (IFE), both oxytetracycline (OTC) and tetracycline (TC) can effectively and rapidly quench the fluorescence of N-SiQDs at 380nm. However, interestingly, the accompanied formation of a new complex of OTC with N-SiQDs could emit fluorescence at 505nm, resulting in a gradualcolor change of the sensor from blue to yellow under the irradiation of 365nm UV lamp. Thus, a visual semi-quantitative detection of OTC was realized. In contrast, based on the aggregation-induced luminescence (AIE) effect, chlortetracycline (CTC) linearly enhanced the fluorescence intensity of N-SiQDs, which can effectively reduce other interfering signals, and can significantly improve the sensitivity and selectivity. Hence, a low limit of detection of 47nM for CTC was obtained. On account of the three distinctly different phenomena and mechanisms of N-SiQDs sensor exhibited towards OTC, TC, and CTC, a novel sensing method for discriminating and selectively measuring OTC, TC, and CTC in food was developed.

Physical-information model of the immune system as a development of P.K. Anokhin’s theory of functional systems

The article deals with the standard immunological model, which is based on the principles of random combination of molecules and cells and their random encounter with their complementary sites, which is accompanied by the formation of reversible complexes and/or a cascade of subsequent reactions. In its purity, such a model gives rise to various kinds of paradoxes that do not correspond to the reality of immune processes. As a rule, the development of immunology is expressed in the construction of more and more detailed links of immunologic events, but the addition of each new event to the chain of links should lead not to acceleration, but to slowing down of the final process within the combinatorial-complementary system. In this connection, the question of a new possible model of the immune system is raised, which is based on P.K. Anokhin’s theory of functional systems. As its further development the physical-information model (PhIM) of the immune system is proposed, which assumes two plans, informational and physical, of the immune system organization and their coordination on the basis of the ideas of organic potential and processes of conjugation. The information plan is represented as an abstract space of degrees of freedom of the system, analogous to phase space in physics. The current and final state of the system can be represented as points of the state space, the activity of the system with the transition from the current to the final state, as a trajectory in this space. The acceptor of the action result in the theory of functional systems of P.K. Anokhin is connected in this case with the image of the final state as the result of the system action. The construction of the trajectory of the system’s activity can be represented as the direction of reduction of the organic potential of the system, by analogy with that in the case of physical systems and their physical potentials. The organic potential reaches a minimum in the final state and expresses the need of the biosystem as a result of action.

Lessons from IgA Nephropathy Models

IgA nephropathy (IgAN) is the most common type of primary glomerulonephritis worldwide; however, the underlying mechanisms of this disease are not fully understood. This review explores several animal models that provide insights into IgAN pathogenesis, emphasizing the roles of aberrant IgA1 glycosylation and immune complex formation. It discusses spontaneous, immunization, and transgenic models illustrating unique aspects of IgAN development and progression. The animal models, represented by the grouped ddY (gddY) mouse, have provided guidance concerning the multi-hit pathogenesis of IgAN. In this paradigm, genetic and environmental factors, including the dysregulation of the mucosal immune system, lead to increased levels of aberrantly glycosylated IgA, nephritogenic immune complex formation, and subsequent glomerular deposition, followed by mesangial cell activation and injury. Additionally, this review considers the implications of clinical trials targeting molecular pathways influenced by IgAN (e.g., a proliferation-inducing ligand [APRIL]). Collectively, these animal models have expanded the understanding of IgAN pathogenesis while facilitating the development of therapeutic strategies that are currently under clinical investigation. Animal-model-based studies have the potential to facilitate the development of targeted therapies with reduced side effects for IgAN patients.

Locating the stigmatisation of children born of wartime rape on a continuum of violence

ABSTRACT Children born of wartime sexual violence remain a marginalised group whose lives and needs have largely been overlooked. Over the past two decades, scholarship has emerged addressing some of the multiple issues they face. This research shows that stigmatisation is central in the children’s lives, but rarely provides a deeper definition of stigma that interrogates its structural and political dimension. Bridging feminist peace scholarship and new streams of stigma research, this article sets out to conceptualise stigmatisation as a complex form of violence that concurrently reflects and reproduces gendered power dynamics across the peace–war spectrum. Drawing on narratives by children born of war in the Central African Republic, Uganda, and Bosnia-Herzegovina, this article examines how stigmatisation materialises as different forms of ‘everyday violence’ that intersects at a personal, social, and structural level. By untangling their stories, the study shows how stigmatisation profoundly impacts the children’s experiences of peace and sustains the ‘conditions of war’ in the everyday space while perpetuating structural cycles of gender-based violence that persists in transitional and post-conflict environments. The article highlights the importance of placing the children’s perspectives at the centre when analysing stigmatisation and offers new insight on how stigma operates as violence.

Gradient dynamics approach to reactive thin-film hydrodynamics

Wetting and dewetting dynamics of simple and complex liquids is described by kinetic equations in gradient dynamics form that incorporates the various coupled dissipative processes in a fully thermodynamically consistent manner. After briefly reviewing this, we also review how chemical reactions can be captured by a related gradient dynamics description, assuming detailed balanced mass action type kinetics. Then, we bring both aspects together and discuss mesoscopic reactive thin-film hydrodynamics illustrated by two examples, namely, models for reactive wetting and reactive surfactants. These models can describe the approach to equilibrium but may also be employed to study out-of-equilibrium chemo-mechanical dynamics. In the latter case, one breaks the gradient dynamics form by chemostatting to obtain active systems. In this way, for reactive wetting we recover running drops that are driven by chemically sustained wettability gradients and for drops covered by autocatalytic reactive surfactants we find complex forms of self-propulsion and self-excited oscillations.

The interaction between beta-ionone and 2-hydroxypropyl-beta-cyclodextrin during the formation of the inclusion complex

As an aroma material, beta-ionone also has a range of pharmacological activities. To solve its problems such as low bioavailability, water-immiscibility, thermo-instability, and volatility, beta-ionone was successfully encapsulated in 2-hydroxypropyl-beta-cyclodextrin (HP-beta-CD) in our previous work. However, the structure of the product, the interaction between beta-ionone and HP-beta-CD, and the mechanism of action were not clear. In this paper, in order to gain a more profound understanding of the structure and chemical behavior of beta-ionone-HP-beta-CD inclusion complex, the interaction between beta-ionone and HP-beta-CD was investigated by molecular simulation. The optimized structures, binding energy, deformation energy, charge transfer, frontier orbital energy gap, chemical hardness, chemical potential, and electrophilicity index were obtained. In the complex, beta-ionone denotes electrons to HP-beta-CD and carries a positive charge. The negative chemical potential of inclusion complex indicates that complex process is spontaneous. The complex shows a relatively higher reactivity and electrophilicity than beta-ionone and HP-beta-CD.

Uranium removal from contaminated groundwater using goethite-loaded composite microporous membrane

In this study, we have coupled adsorption and membrane separation for the removal of uranium from contaminated groundwater in environmentally relevant conditions at low energy requirements. This study mainly focuses on elucidating uranium, U(VI), adsorption mechanisms using surface complexation modeling approach in a novel goethite-loaded composite microfiltration membrane (GLM). This experiment involved immobilizing goethite nanorods in a microporous (0.22 μm pore size) poly (vinylidene fluoride) (PVDF) membrane. The effect of varying goethite loading and hydraulic residence time on U(VI) removal was investigated at field-relevant pH (i.e. pH 8.5). U(VI) adsorption (i.e. 4.95 μg·mg−1) was optimum at a goethite loading 1.20 mg·cm−2. The effect of varying hydraulic residence time had no impact on U(VI) removal which was also confirmed via performing batch adsorption kinetic experiments. GLM membrane loaded at 1.2 mg·cm−2 could treat 275 L of U(VI) contaminated water having 200 μg of U L−1 below WHO drinking water limit (i.e. 30 μg of U L−1) with 1 m2 of membrane surface area with a adsorption capacity of 6.12 μg·mg−1. Varying the pH of aqueous solution, containing U(VI) from pH 4.0 to pH 10.0, showed a significant impact on uranium uptake ranging from 0.7 μg·mg−1 to 2.63 μg·mg−1 by the composite membrane. The adsorption mechanism of uranium onto goethite was explained via the formation of bidentate surface complexes using the Surface Complexation Model (SCM). The results of batch pH edge experiments and SCM have been compared with pH experiments performed using GLM. The results of SCM predicted the batch pH edge experiment within a RMSE of 0.055. The trend of U(VI) removal in membrane experiments was observed to be similar to that of batch pH edge experiments and was well predicted SCM model. Our results showed that the novel goethite-loaded membrane has the potential for the effective removal of uranium with a lower specific energy consumption.

In Silico Modeling of Myelin Oligodendrocyte Glycoprotein Disulfide Bond Reduction by Phosphine-Borane Complexes

Background: Neurodegenerative diseases can cause vision loss by damaging retinal ganglion cells in the optic nerve. Novel phosphine-borane compounds (PBs) can protect these cells from oxidative stress via the reduction of disulfide bonds. However, the specific targets of these compounds are unknown. Proteomic evidence suggests that myelin oligodendrocyte glycoprotein (MOG) is a potential target. MOG is of significant interest due to its role in anti-MOG optic neuritis syndrome. Methods: We used in silico modeling to explore the structural consequences of cleaving the extracellular domain MOG disulfide bond, both in isolation and in complex with anti-MOG antibodies. The potential binding of PBs to this bond was examined using molecular docking. Results: Cleaving the disulfide bond of MOG altered the structure of MOG dimers and reduced their energetic favorability by 46.13 kcal/mol. The energy profiles of anti-MOG antibody complexes were less favorable when the disulfide bond of MOG was reduced in the monomeric state by 55.21 kcal/mol, but the reverse was true in the dimeric state. PBs exhibited reducing capabilities with the MOG extracellular disulfide bond, with this best-scoring compound binding with an energy of −28.54 kcal/mol to the MOG monomer and −24.97 kcal/mol to the MOG dimer. Conclusions: These findings suggest that PBs can affect the structure of MOG dimers and the formation of antibody complexes by reducing the MOG disulfide bond. Structural changes in MOG could have implications for neurodegenerative diseases and anti-MOG syndrome.

DNA supercoiling enhances DNA condensation by ParB proteins.

The ParABS system plays a critical role in bacterial chromosome segregation. The key component of this system, ParB, loads and spreads along DNA to form a local protein-DNA condensate known as a partition complex. As bacterial chromosomes are heavily supercoiled due to the continuous action of RNA polymerases, topoisomerases and nucleoid-associated proteins, it is important to study the impact of DNA supercoiling on the ParB-DNA partition complex formation. Here, we use an in-vitro single-molecule assay to visualize ParB on supercoiled DNA. Unlike most DNA-binding proteins, individual ParB proteins are found to not pin plectonemes on supercoiled DNA, but freely diffuse along supercoiled DNA. We find that DNA supercoiling enhances ParB-DNA condensation, which initiates at lower ParB concentrations than on DNA that is torsionally relaxed. ParB proteins induce a DNA-protein condensate that strikingly absorbs all supercoiling writhe. Our findings provide mechanistic insights that have important implications for our understanding of bacterial chromosome organization and segregation.

Pediatric Orally Disintegrating Tablets (ODTs) with Enhanced Palatability Based on Propranolol HCl Coground with Hydroxypropyl-β-Cyclodextrin

Background: Propranolol, largely prescribed as an antihypertensive and antiarrhythmic drug in pediatrics, is characterized by a bitter taste and an astringent aftertaste. Currently, the therapy requires crushing of tablets for adults and their dispersion in water many times a day, leading to loss of dosing accuracy, low palatability, and poor compliance for both patients and caregivers. Objectives: This work aimed to exploit cyclodextrin complexation by cogrinding to develop orally disintegrating tablets (ODTs) endowed with reliable dosing accuracy, good palatability and safety, ease of swallowability, and ultimately better compliance for both pediatric patients and caregivers. Results: Different formulation variables and process parameters were evaluated in preparing ODTs. The technological and morphological characterization and disintegration tests were performed according to official and alternative tests to select the ODT formulation based on the drug Hydroxypropyl-β-cyclodextrin (HPβCD) coground complex form containing Pearlitol® Flash as the diluent and 8% Explotab® as the superdisintegrant, which demonstrated the highest % drug dissolution in simulated saliva and acceptable in vitro palatability assessed by the electronic tongue, confirming the good taste-masking power of HPβCD towards propranolol. Conclusions: Such a new dosage form of propranolol could represent a valid alternative to the common extemporaneous preparations, overcoming the lack of solid formulations of propranolol intended for pediatric use.

Bimetallic Uranium Complexes with 2,6-Dipicolinoylbis(N,N-Dialkylthioureas)

2,6-Dipicolinoylbis(N,N-dialkylthioureas), H2LR, readily react with uranyl salts under formation of monomeric or dimeric complexes of the compositions [UO2(LR)(solv)] (solv = donor solvents such as H2O, MeOH or DMF) or [{UO2(LR)(µ-OMe)}2]2− (1). In such complexes, the uranyl ions are exclusively coordinated by the “hard” O,N,O or N,N,N donor atom sets of the central ligand unit and the lateral sulfur donor atoms do not participate in the coordination. Different conformations have been found for the dimeric anions. The bridging methanolato ligands and the four uncoordinated sulfur atoms can adopt different orientations with respect to the equatorial coordination spheres of the uranyl units. The presence of non-coordinated sulfur atoms offers the opportunity for the coordination of additional, preferably “soft” metal ions. Thus, reactions with [AuCl(PPh3)], lead acetate or acetates of transition metal ions such as Ni2+, Co2+, Fe2+, Mn2+, Zn2+, or Cd2+, were considered for the syntheses of bimetallic complexes. Various oligometallic complexes with uranyl units were prepared: [{UO2(LR)(μ-OMe)(Au(PPh3)}2] (2), [(UO2)3Pb2(LR)4(MeOH)2(μ-OMe)2] (3), [M{UO2(LR)(OAc)}2] (M= Zn, Ni, Co, Fe, Mn or Cd) (R = Et: 5, RR = morph: 6), or [(UO2)(NiI)2(LR)2] (7). The products were extensively studied spectroscopically and by X-ray diffraction.

Computational study of the encapsulation of an organic polluant with beta-CD, in vacuum and in water

This article reports the results of a theoretical study of the host/guest inclusion complex involving a herbicide called Diuron in β-cyclodextrin. Various computational techniques were used to determine the structure, geometry and stability energies of the complex. The analysis of the diuron/β-CD inclusion complex was performed both in vacuum and in water in a 1:1 ratio. The DFT/B97-3C method was used to obtain the structures of the complexes and to calculate their stability energies. The specific configurations were determined using nuclear magnetic resonance spectroscopy. The interaction bonds were investigated and the formation of conventional hydrogen bonds was detected by AIM analysis. The nature of the interactions was further elucidated using the method of non-covalent interactions (NCI). This showed that hydrogen bonds and van der Waals interactions contribute significantly to the formation of the inclusion complex. To gain more insight into the absorption and emission energies of the investigated complex, the gap energy (EHOMO-ELUMO) was calculated.

Study of Complexation Patterns in the System Ni2+, MoO42–, P2O74–, Cit3–for the Development of Poly-Ligand Electrolytes (Study of complexation patterns)

The complexation behavior in systems containing Ni2+, MoO42−, P2O74−, Cit3− - ions have been thoroughly investigated. The study determined the composition and instability constants of both mono- and biligand complex compounds at a constant ionic strength of the solution (Ic=1). By analyzing the concentration ratios of the complexing agent and ligands, the composition of mono- and polyligand complexes was elucidated. The complexation study utilized the potentiometric method, which is based on the functional dependence of the potential of the indicator electrode on the concentration of the complexing agent ions. The results enabled the calculation of the ionic composition of aqueous solutions of nickel complexes with citrate and diphosphate ions, depending on their concentrations. A proposed scheme for the formation of heteronuclear nickel-molybdenum complexes takes into account the sequence of component introduction into the electrolyte to form complexes of a specific composition. These findings were applied to develop electrolyte compositions for coating with alloys based on iron subgroup metals with molybdenum. These alloys exhibit several valuable properties, including corrosion resistance, electrocatalytic activity in hydrogen production, and enhanced operational characteristics.

The synergistic immunomodulatory activity of Lycium barbarum glycopeptide and isochlorogenic acid A on RAW264.7 cells.

Regulation of the immune system to maintain homeostasis in the organism has become a focus of research, and the synergistic effect of multi-component complexes will effectively improve the immunomodulatory activity. The present study aimed to investigate the interaction and synergistic immunomodulatory activity of isochlorogenic acid A (IAA) and Lycium barbarum glycopeptide (LbGp). The results obtained indicated that non-covalent intermolecular interactions were employed to form the LbGp-IAA complex, with a binding ratio of 135.15 mg g-1. The formation of LbGp-IAA complex altered the conformation of LbGp, and IAA was mainly bound to LbGp by van der Waals forces and hydrogen bonds. In addition, LbGp-IAA promoted the proliferation of RAW264.7 cells. The IAA and LbGp interaction had a synergistic effect on the promotion of phagocytosis and the expression of nitric oxide, tumor necrosis faction-α and interleukin-1β, which improved the immunomodulatory effect of LbGp. Furthermore, the combination of LbGp and IAA synergistically inhibited lipopolysaccharide-induced inflammatory response. In summary, the binding of IAA enhanced the immunomodulatory activity of LbGp and coordinated the immune response, and did not trigger an inflammatory response, which was potentially attributed to the alteration of spatial structure of LbGp through the binding of IAA. The results provide new perspectives for the study of glycopeptide-polyphenol interactions. © 2024 Society of Chemical Industry.

Indigestible proteins and peptide-bound AGEs in ultra-processed foods: Dulce de leche as a model of severely transformed protein food systems

Caramel milk confectioneries, such as dulce de leche, are produced by simmering whole or reconstituted milk with sugar and alkali at temperatures ranging from 115 to 130 °C for several hours. This process triggers extensive non-enzymatic browning through the Maillard reaction, leading to significant modifications in milk proteins. Our research focused on the effects of such severe processing conditions on the structural integrity and digestibility of milk proteins, using dulce de leche as a model for severely transformed food protein systems. Due to structural modifications, covalent interchain cross-links, and sugar-derived bridging moieties, milk proteins in dulce de leche form high molecular weight aggregates that are not resolvable by SDS-PAGE. Proteomic analysis revealed that all major milk proteins are involved in the formation of these covalent molecular complexes. When subjected to static gastro-duodenal digestion using both adult and infant models, these macroaggregates showed resistance to pepsin and marginal susceptibility to duodenal proteases. High pressure liquid chromatography-tandem mass spectrometry (HPLC-MS/MS)-based peptidomic analysis of dulce de leche digests allowed identifying variously sized polypeptides bearing the hallmarks of the Maillard reaction. However, many MS signals could not be assigned due to unknown modifications. The prevalence of free and peptide-bound advanced glycated end products (AGEs) in caramel milk products and other ultra-processed foods poses significant health concerns, stressing the need for a comprehensive dedicated evaluation.

Effect of Anions on Deformation of Gallium-Based Liquid Metal in Solution.

In this study, deformation behaviors of gallium-based liquid metals in acidified cupric sulfate or cupric chloride solutions with varying concentrations of chloride anion or sulfate anion were investigated to explore their potential applications in soft machines and electronics. Gallium-based liquid metals are known for their unique deformability, making them promising materials for various fields. Previous research has shown that deformation of the liquid metal can be achieved in the presence of acidified cupric or ferric salts. However, the specific influence of different anions on the deformation process remains unclear. Our findings indicate that the deformation rate of the liquid metal increases with higher concentrations of chloride ions and decreases with higher concentrations of sulfate ions in the solution. UV-vis absorbance spectra of the solutions were analyzed to identify the formation of hydrated cupric cations. It was observed that increasing the concentration of Cl- ions promotes the formation of cupric-chloro complexes, thereby reducing the concentration of hydrated cupric ions in the solution. Furthermore, the addition of sulfate ions to the solution enhances the ionic strength of the medium, leading to the dissociation of cupric-chloro complexes. Additionally, sulfate ions can form insoluble layers with gallium ions, which impede the deformation of the liquid metal. The deformation rate of the liquid metal was found to be inversely correlated with the concentration of cupric ions in the solution. These results provide valuable insights into the deformable behavior of gallium-based liquid metals and their potential applications in liquid metal-based soft robots. This study highlights the importance of understanding the role of different anions in the deformation process of liquid metals, shedding light on the design and optimization of soft machines and electronics utilizing these materials.

ExoLyn: A golden mean approach to multispecies cloud modeling in atmospheric retrieval

Clouds are ubiquitous in exoplanets' atmospheres and play an important role in setting the opacity and chemical inventory of the atmosphere. Understanding clouds is a critical step in interpreting exoplanets' spectroscopic data. The aim is to model the multispecies nature of clouds in atmospheric retrieval studies. To this end, we developed -- a 1D cloud model that balances physical consistency with computational efficiency. solves the transport equation of cloud particles and vapor under cloud condensation rates that are self-consistently calculated from thermodynamics. is a standalone, open source package capable of being combined with optool to calculate solid opacities and with petitRADTRANS to generate transmission or emission spectra. With we find that the compositional structure of clouds in hot Jupiter planets' atmospheres is layered with a cloud dominated by magnesiumsilicates on top of an iron cloud. This finding is consistent with more complex cloud formation models but can be obtained with in only a few seconds. The composition of the cloud particles can be constrained from the spectrum, for example MgSiO3 and Mg2SiO4 components give rise to an absorption feature at $8-10\ m $. We investigate the dependence of the cloud structure on the bulk elemental composition of the planet and find that SiO2 -dominated clouds form on metal-rich planets and Fe clouds with a strong extinction effect form on C-rich planets. Designed toward maximum flexibility can also be used in retrieval analysis of sub-Neptunes and self-luminous planets. The efficiency of opens the possibility of joint retrieval of exoplanets' gas and cloud components.