Copper Metal Research Articles

AuNPs@MoS2 functionalized copper metal organic framework for boosting electrocatalytic glucose oxidation

A novel non-enzyme glucose sensor based on functionalized copper metal–organic framework composite material, AuNPs@MoS2/Cu-MOF, was developed for rapid glucose analysis. Cu-MOF nanomaterial was prepared via a hydrothermal method, followed by the surface loading of core–shell structured AuNPs@MoS2 to synthesize AuNPs@MoS2/Cu-MOF composite material. Consequently, a novel gold nanoparticle @ molybdenum disulfide/copper metal–organic framework (AuNPs@MoS2/Cu-MOF/GCE) non-enzyme glucose sensor was constructed. Scanning electron microscopy (SEM), energy dispersive spectrometer (EDS) and X-ray powder Diffraction (XRD) was used to verify that the non-enzyme glucose sensor had been constructed effectively. Traditional electrochemical characterization methods were employed to study the electrocatalytic performance of the AuNPs@MoS2/Cu-MOF/GCE sensor and its catalytic oxidation of glucose. The experimental results demonstrated a good linear correlation between the concentration of glucose and the peak current within the range of 0.05–14.85 mM, with a detection limit of 16.7 μM. The AuNPs@MoS2/Cu-MOF/GCE sensor exhibited rapid electrochemical response to glucose (within 0.5 s), along with long-term stability and excellent selectivity. This is because Cu(II) in Cu-MOF can serve as active sites for the electrocatalytic oxidation of glucose, while the core–shell structure of AuNPs@MoS2 with excellent conductivity can lower the energy barrier in the reaction, further accelerating this catalytic reaction. The AuNPs@MoS2/Cu-MOF/GCE sensor is cost-effective, easy to operate, and suitable for accurate rapid quantification of glucose.

Comprehensive research of the distribution of tellurium-bismuth mineralization in the ores of the Abyz and Maleevskoe sulfide deposits (Republic of Kazakhstan)

Abstract. Within the formations of ensimatic and ensialic island arcs in the territory of Central and Northern Kazakhstan, there are more than thirty pyrite deposits enriched in copper, lead, zinc, gold, silver and rare metal mineralization, which is still insufficiently studied. Relevance. The need to replenish information on tellurium-bismuth mineralization in ores of sulfide deposits formed in ensimatic (Abyz deposit) and ensialic (Maleevskoe deposit) island-arc systems, to establish a spatial connection of this type of mineralization with geodynamic conditions and predict the potential for their associated extraction from ore. Aim. To study and compare morphological characteristics, distribution patterns and conditions for the formation of tellurium-bismuth mineralization in ores of pyrite deposits formed in different island-arc geodynamic settings. Methods. Inductively coupled plasma mass spectrometry, mineragraphic and mineralogical analyses, scanning electron microscopy in combination with X-ray spectral microanalysis, Raman spectroscopy, thermobarogeochemical studies. Results. A comparison of the pyrite deposits of the Rudno-Altai and Chingiz-Tarbagatai island arc systems showed many similarities and differences between them. The deposits have a multi-stage formation and a similar mechanism of ore deposition with similar physicochemical conditions for the formation of tellurium-bismuth mineralization. A spatial relationship between Te-Bi mineralization and geodynamic settings was established: for deposits associated with paleooceanic structures, a predominance of the tellurium element is observed, and for continental rifts, a predominance of the bismuth element.

Heterogenous Copper(0)-Assisted Dopamine Oxidation: A New Pathway to Controllable and Scalable Polydopamine Synthesis.

In this study, we introduce an approach for synthesizing polydopamine (PDA) through the controlled oxidation of dopamine using metallic copper. Traditional methods of PDA synthesis often encounter challenges such as scalability, reproducibility, and control over polymerization. Our approach utilizes the catalytic properties of metallic copper in the presence of dissolved oxygen to generate reactive oxygen species (ROS) without additional chemicals. This process allows for precise control over dopamine oxidation, leading to reliable, materials and cost-effective upscalable PDA production. We investigated the reaction kinetics and the role of copper and ROS in dopamine oxidation, using several different experimental techniques. Our results demonstrate that, even at low pH, the copper-assisted method produces PDA with properties comparable to those synthesized through conventional means. We propose a mechanism for PDA synthesis that is initiated by oxygen adsorption onto copper surface, leading to the generation of various ROS which act as oxidizing agents in PDA synthesis. This method presents an advancement in the scalable and controlled production of PDA, with potential applications in various scientific and industrial fields.

Copper-Catalyzed Asymmetric Hydrogenation of Unsymmetrical ortho-Br Substituted Benzophenones.

The asymmetric hydrogenation of benzophenones, catalyzed by low-activity earth-abundant metal copper, has hitherto remained a challenge due to the substrates equipped with two indistinguishably similar aryl groups. In this study, we demonstrated that the prochiral carbon of the ortho-bromine substrate exhibits the highest electrophilicity and high reactivity among the ortho-halogen substituted benzophenones, as determined by the Fukui function (f+) analysis and hydrogenation reaction. Considering that the enantiodirecting functional bromine group can be easily derivatized and removed in the products, we successfully achieved a green copper-catalyzed asymmetric hydrogenation of ortho-bromine substituted benzophenones. This method yielded a series of chiral benzhydrols with excellent results. The utility of this protocol has been validated through a gram-scale reaction and subsequent product transformations. Hirshfeld partition (IGMH) and energy decomposition analysis (EDA) indicate that the CH···HC multiple attractive dispersion interactions (MADI) effect between the catalyst and substrate enhances the catalyst's activity.

Source and Influencing Factor Analysis of Soil Heavy Metals Based on PMF Model and GeoDetector

In Lijiang City, as a typical example, 93 soil samples were collected from the study area, and soil pH； organic matter； and heavy metals arsenic （As）, mercury （Hg）, copper （Cu）, zinc （Zn）, lead （Pb）, cadmium （Cd）, and chromium （Cr） were determined. We explored the sources of heavy metals in the study area by means of Positive Definite Matrix Factorization （PMF） modeling and analyzed the impact of influencing factors by combining seven heavy metals with 13 influencing factors in a GeoDetector. The results showed that the mean values of soil heavy metals ω（As）, ω（Hg）, ω（Cu）, ω（Zn）, ω（Pb）, ω（Cd）, and ω（Cr） in the study area were 17.55, 0.19, 86.75, 164.84, 28.95, 0.39, and 167.87 mg·kg-1, respectively, which were greater than the background values of soils in Yunnan Province （except for As and Pb）. Regarding spatial distribution, the high values of Cu and Cr content were mainly concentrated in Yulong Naxi Autonomous County； the high value areas of As, Hg, Pb, and Cd were mainly concentrated in Ninglang Yi Autonomous County； and the high value of Zn content was mainly concentrated in Huaping County. Correlation analysis and PMF modeling revealed that the main sources of heavy metals As and Hg in the study area were industrial sources, Zn was from transportation pollution sources, Cr and Cu were from natural sources, and Cd and Pb were from agricultural sources. Further, the factor detector of the GeoDetector found that soil pH and organic matter （OC） had strong explanatory power for the content of seven heavy metals, and the interaction detector found that the results following the interaction of different influencing factors were nonlinear enhancement or two-factor enhancement, in which the interaction of OC and pH was the dominant factor for the spatial differentiation of heavy metals. This provides an important scientific basis for the protection of the soil environmental health and sustainable development in Lijiang City.

Comparative assessment of phytoremediation potential of four Ficus spp. under Semi-arid environmental conditions.

Heavy metals have been recognized as a prominent hazard in today's world, causing pollution in the air environment. Woody tree species can play a significant role in the extraction and remediation of metal pollutants from the air, therefore promoting the air quality index. This study investigated the potential of four species of the Ficus genus (F. benjamina, F. microcarpa, F. religiosa, and F. virens) to remediate varying levels of heavy metal contamination in industrial, residential, and highway areas of Faisalabad City, Pakistan. For this purpose, six heavy metals (cadmium, chromium, copper, lead, zinc, and manganese) were assessed in young leaves (YL) as well as old leaves (OL) of subjected tree species at selected study sites. Eight fully expanded leaves were selected from each tree species: two from each cardinal direction from the shoot of the current year (young leaves, YL), as well as from the shoot of the previous year (old leaves, OL). The results showed that the same genus has different capabilities to accumulate different heavy metals, and the overall trend was in the following order: F. virens > F. religiosa > F. benjamina > F. microcarpa at all study sites. The heavy metal contents in both YL and OL of selected tree species decreased in the order of Manganese (Mn)> Zinc (Zn)> Copper (Cu) > Chromium (Cr) > Lead (Pb) > Cadmium (Cd) at all study sites. The metal accumulation index (MAI) values ranged between 2.14-5.42 for F. benjamina, 2.09-3.89 for F. microcarpa, 3.61-7.01 for F. religiosa and 4.77-6.48 for F. virens across all study sites. Among the studied tree species, it has been determined that F. virens and F. religiosa are well-suited for urban areas with significant heavy metal contamination and can be strategically planted in barrier areas to effectively combat atmospheric pollution.

Stabilized Cu0 -Cu1+ dual sites in a cyanamide framework for selective CO2 electroreduction to ethylene

Electrochemical reduction of carbon dioxide to produce high-value ethylene is often limited by poor selectivity and yield of multi-carbon products. To address this, we propose a cyanamide-coordinated isolated copper framework with both metallic copper (Cu0) and charged copper (Cu1+) sites as an efficient electrocatalyst for the reduction of carbon dioxide to ethylene. Our operando electrochemical characterizations and theoretical calculations reveal that copper atoms in the Cuδ+NCN complex enhance carbon dioxide activation by improving surface carbon monoxide adsorption, while delocalized electrons around copper sites facilitate carbon-carbon coupling by reducing the Gibbs free energy for *CHC formation. This leads to high selectivity for ethylene production. The Cuδ+NCN catalyst achieves 77.7% selectivity for carbon dioxide to ethylene conversion at a partial current density of 400 milliamperes per square centimeter and demonstrates long-term stability over 80 hours in membrane electrode assembly-based electrolysers. This study provides a strategic approach for designing catalysts for the electrosynthesis of value-added chemicals from carbon dioxide.

The early medieval origins of copper ore extraction in the Carpathian Mountains

The case study addresses the question of the early medieval revival of copper production in Europe. The focus of the research area is the Carpathian Basin, located on the eastern periphery of the zone influenced by European early medieval processes. The research of where and when early medieval metal production started in the region in our case also provides answers to the question of how the region was linked to the European continental economic network, which is until recently an unresolved problem. Ore extraction and the production of various non-ferrous metals (copper, silver, gold) had important centres in the Carpathian Mountains throughout the Middle Ages until the Modern Era. Concerning the Avar period, our study comprises lead isotope and chemical analyses of ‘Late Avar’ (c. 8th century AD) copper rivets, used for certain purposes alongside the copper alloys predominant in the period. As rivets were selected from the entire Avar cultural area, expanding virtually to all lowland and hilly areas in the Carpathian Basin, results are representative of the entire region. It shows that Avar craftsmen producing large quantities of copper alloy objects in the 8th and the early 9th century were supplied with copper from a single mining district, from the ore deposits of the Slovak Ore Mountains in the today Central Slovakia, a region which became an important metal-processing centre in the 11th century AD.

Profile of Bacterial Communities in Copper Mine Tailings Revealed through High-Throughput Sequencing.

Mine-tailing dumps are one of the leading sources of environmental degradation, often with public health and ecological consequences. Due to the complex ecosystems generated, they are ideal sites for exploring the bacterial diversity of specially adapted microorganisms. We investigated the concentrations of trace metals in solid copper (Cu) mine tailings from the Ovejería Tailings Dam of the National Copper Corporation of Chile and used high-throughput sequencing techniques to determine the microbial community diversity of the tailings using 16S rRNA gene-based amplicon sequence analysis. The concentrations of the detected metals were highest in the following order: iron (Fe) > Cu > manganese (Mn) > molybdenum (Mo) > lead (Pb) > chromium (Cr) > cadmium (Cd). Furthermore, 16S rRNA gene-based sequence analysis identified 12 phyla, 18 classes, 43 orders, 82 families, and 154 genera at the three sampling points. The phylum Proteobacteria was the most dominant, followed by Chlamydiota, Bacteroidetes, Actinobacteria, and Firmicutes. Genera, such as Bradyrhizobium, Aquabacterium, Paracoccus, Caulobacter, Azospira, and Neochlamydia, showed high relative abundance. These genera are known to possess adaptation mechanisms in high concentrations of metals, such as Cd, Cu, and Pb, along with nitrogen-fixation capacity. In addition to their tolerance to various metals, some of these genera may represent pathogens of amoeba or humans, which contributes to the complexity and resilience of bacterial communities in the studied Cu mining tailings. This study highlights the unique microbial diversity in the Ovejería Tailings Dam, including the discovery of the genus Neochlamydia, reported for the first time for heavy metal resistance. This underscores the importance of characterizing mining sites, particularly in Chile, to uncover novel bacterial mechanisms for potential biotechnological applications.

Accelerating Relativistic Exact-Two-Component Density Functional Theory Calculations with Graphical Processing Units.

Numerical integration of the exchange-correlation potential is an inherently parallel problem that can be significantly accelerated by graphical processing units (GPUs). In this Letter, we present the first implementation of GPU-accelerated exchange-correlation potential in the GauXC library for relativistic, 2-component density functional theory. By benchmarking against copper, silver, and gold coinage metal clusters, we demonstrate the speed and efficiency of our implementation, achieving significant speedup compared to CPU-based calculations. One GPU card provides computational power equivalent to roughly 400 CPU cores in the context of this work. The speedup further increases for larger systems, highlighting the potential of our approach for future, more computationally demanding simulations. Our implementation supports arbitrary angular momentum basis functions, enabling the simulation of systems with heavy elements and providing substantial speedup to relativistic electronic structure calculations. This advancement paves the way for more efficient and extensive computational studies in the field of density functional theory.

The Copper Metal and Magnetite Nanoparticles Conjugated with Salicylic Acid Composite Stimulated Wheat Defense Mechanism and Affected Cellular Components under Heat Stress

Aims: This study aimed to examine the effect of magnetite coating of salicylic acid and Cu metal nanoparticles on yield, cellular contents, and some biochemical constituents of wheat subjected to heat stress. Background: An applied experiment was conducted over two seasons at the Agricultural Experimental Station of Desert Research Center (DRC), which was supervised by the El Wadi El Gadeed Governorate in Egypt. The grains of wheat cultivars Sids1 (tolerant) and Gimmeza7 (sensitive) were treated with copper metal as NPs (Cu NPs) (0.25, 0.50, 0.75, 1.0, and 10 ppm) and magnetite NPs (0.25, 0.50, 0.75, 1.0 and 10 ppm) coated with salicylic acid at 100ppm (Fe NPs+SA). Objective: The objective of this study was to examine wheat tolerance to heat stress and subsequently yield by comparing two wheat cultivars under the same conditions. Method: The chemically formulated nanoparticles were well characterized and applied in two wheat cultivars subjected to heat stress. Results: The results showed that all NPs treatments had a positive impact on all physiological parameters and grain yield. Sids1 surpassed Gemmeiza7 in the quality of wheat grains (essential, nonessential amino acids). However, Gimmeza7 exceeded Sids1 in yield quantity, especially with the application of SA+Fe NPs at 0.50 ppm. These effects were associated with heat tolerance and the best survival in wheat cultivars. There was an increase in glutathione content, antioxidant enzymes (Glutathione -S- Transferase), and/or a decline in malondialdehyde content. Conclusion: Fe NPs+SA (0.5ppm) helped the Gimmeza7 cultivar to mitigate the effects of heat stress through activating growth, glutathione, and glutathione S transferase, enhancing yield quantity in two wheat cultivars (Misr1 and Gimmeza11), and decreasing their MDA content.

Enhanced mineralization of pharmaceutical residues at circumneutral pH by heterogeneous electro-Fenton-like process with Cu/C catalyst

Conventional electro-Fenton (EF) process at acidic pH ∼3 is recognized as a highly effective strategy to degrade organic pollutants; however, homogeneous metal catalysts cannot be employed in more alkaline media. To overcome this limitation, pyrolytic derivatives from metal-organic frameworks (MOFs) have emerged as promising heterogeneous catalysts. Cu-based MOFs were prepared using trimesic acid as the organic ligand and different pyrolysis conditions, yielding a set of nano-Cu/C catalysts that were analyzed by conventional methods. Among them, XPS revealed the surface of the Cu/C-A2-Ar/H2 catalyst was slightly oxidized to Cu(I) and, combined with XRD and HRTEM data, it can be concluded that the catalyst presents a core-shell structure where metallic copper is embedded in a carbon layer. The antihistamine diphenhydramine (DPH), spiked into either synthetic Na2SO4 solutions or actual urban wastewater, was treated in an undivided electrolytic cell equipped with a DSA-Cl2 anode and a commercial air-diffusion cathode able to electrogenerate H2O2. Using Cu/C as suspended catalyst, DPH was completely degraded in both media at pH 6–8, outperforming the EF process with Fe2+ catalyst at pH 3 in terms of degradation rate and mineralization degree thanks to the absence of refractory Fe(III)-carboxylate complexes that typically decelerate the TOC abatement. From the by-products detected by GC/MS, a reaction sequence for DPH mineralization is proposed.

Fractal Growth Regulation and Mechanism of Copper Dendrite by Micro‐point Electrode Electrodeposition

AbstractThe behavior of fractal growth based on copper metal was examined by micro‐point electrode electrodeposition. On this basis, the process and morphological characteristic of Cu fractal growth can be controlled by changing the electrodeposition time, current and concentration of Cu2+. The growth of snowflake Cu dendrites is confined to the two‐dimensional plane of the paper base to monitor the fractal structural changes. The electrodeposition process of snowflake Cu dendrites is deeply regulated by exploring the changing trend of fractal dimension. To further understand the fractal growth mechanism of Cu, the electro‐driven centripetal migration and random migration of ions are introduced in the traditional diffusion‐limited aggregation model. The simulated fractal patterns successfully correspond with the experimental results. The results are helpful to explore the fractal growth characteristics and dynamic mechanism of the electrodeposited copper dendrites, which lay a foundation for controlling the growth of the electrodeposited metal dendrites.

ANTIVIRAL TEXTILES AND ANTIVIRAL ACTIVITY TESTING - THE USE OF BACTERIOPHAGE SURROGATE FOR ANTIVIRAL ACTIVITY TESTING

The risk of dissemination of highly contagious viral diseases (as COVID-19, Ebola) led in the increasing need to develop functional textiles and surfaces with antiviral effect. Antiviral textiles are designed to reduce the viability and infectivity of viruses on their surfaces and by this way to reduce the cases of infection (including re-infection or cross-infection with contaminated textiles). Different antiviral agents and diverse techniques of their application are used for functionalized textiles manufacturing. The most often used antivirals are metallic and ionic silver and copper, iron oxide, quaternary ammonium salts. The aim of the process is to prepare textiles with long-term durable finishing effective in viral activity inhibition. The basic step of functionalized antiviral textiles development is antiviral effectivity testing. The safe method of testing with the use of Phi6 bacteriophage, SARS-CoV-2 and Ebola virus surrogate, was modified for antiviral textiles testing. The samples of textiles with antiviral finishing were tested by the bacteriophage-based method and excellent antiviral activity was detected for all tested materials. The woven cotton was used as reference untreated material, the different textile cotton structures with similar square weight were compared and no statistically significant difference was found between the resulting antiviral efficacy values. A simple and quickly feasible screening method for determining the antiviral properties of textiles, especially with leaching-type of treatment, was also designed and tested.

Source identification of heavy metal contamination in beach sediments of the ancient city of Phaselis in Antalya, Türkiye

The ancient city of Phaselis, which is located along gravel, coarse sandy, and sandy beaches, is a popular area visited by thousands of domestic and foreign tourists every year, and has been selected as the study area. Sediment samples collected from 57 different locations in the ancient city of Phaselis were analyzed using an X-ray fluorescence (XRF) spectrometer, and the major, trace, and rare earth element contents of the samples were revealed. The heavy metals arsenic (As), cobalt (Co), chromium (Cr), copper (Cu), nickel (Ni), lead (Pb), tin (Sn), stronsium (Sr), and zinc (Zn) were used in the pollution index calculations. Distribution maps revealed that heavy metal concentrations reached higher levels, especially in the eastern part of the study area. Therefore, it is recommended to plant rooted macrophytes that can absorb the heavy metals Cr and Ni and perform phytoremediation of the sediment in the region.

Rapid assessment of the creep rupture life of metals: A model enabling experimental design

Prediction of the creep rupture life of engineering metals is critical for qualification and design of new materials. The use of long-term creep tests and the need to quantify the performance variability in a priori similar systems hinder the rapid creep assessment of a given material. Therefore, it is essential to develop methods that can extrapolate the long-term performance of alloys and the associated variability from short-term experiments. To this end, this study introduces a new model which enables the estimation of the rupture life of a material for a given stress and temperature. This model relies on two components. First, a new relation for the minimum creep rate (MCR) of materials is introduced. It includes a stress dependent stress exponent allowing the model to capture the variation of MCR across a wide range of temperatures and stresses. Second, employing the Monkman-Grant (MG) law, we establish a relation between stress, temperature and creep rupture life. Together, these two elements yield a new closed-form mathematical expression for the Larson Miller parameter as a function of stress and temperature. This expression captures the creep rupture time for many metals (Gr91, Copper, Gr122 and 347H) and compares favorably with alternate empirical approaches. The model is then used to assess the minimum duration of creep rates necessary to qualify the material up to 100000h. It is found that depending on the material system, creep tests as few as five limited to 5000 h for steels (Gr91, Gr122, 347H) and 100 h for copper are sufficient to model creep lifetimes. Finally, using a Bayesian inference-based approach to calibrate the model, we demonstrate that variability in rupture life can be captured via the quantification of the uncertainty in the model parameters and extrapolated from a limited number of short to moderately short creep tests; thereby paving the way for accelerated creep testing.

Surface Facets Reconstruction in Copper-Based Materials for Enhanced Electrochemical CO2 Reduction.

The unavoidable and unpredictable surface reconstruction of metallic copper (Cu) during the electrocatalytic carbon dioxide (CO2) reduction process is a double-edged sword affecting the production of high-value-added hydrocarbon products. It is crucial to control the surface facet reconstruction and regulate the targeted facets/facet interfaces, and further understand the mechanism between activity/selectivity and the reconstructed structure of Cu for CO2 reduction. Based on the current catalyst design methods, a facile strategy combining chemical reduction and electro-reduction is proposed to achieve specified Cu(111) facets and the Cu(110)/(111) interfaces in reconstructed Cu derived from cuprous oxide (Cu2O). The surface facet reconstruction significantly boosted the electrocatalytic conversion of CO2 into multi-carbon (C2+) products comparing to the unmodified catalyst. Theoretical and experimental analyses show that the Cu(110)/(111)s interface between Cu(110) and a small amount of Cu(111) can tailor the reaction routes and lower the reaction energy barrier of C-C coupling to ethylene (C2H4). The work will guide the surface facets reconstruction strategy for Cu-based CO2 electrocatalysts, providing a promising paradigm to understand the structural variation in catalysts.

Highly conductive copper-coated polyamide yarn for wearable sensing and Joule heating applications

A highly conductive yarn was developed by electroless deposition of copper metal particles on the polyamide 6 yarn. The successful incorporation of Cu particles into the substrate was revealed by surface and elemental characterizations. The Cu/PA 6 yarn exhibited superior electrical conductivity (2.3 Ω/cm) with improved mechanical properties. The excellent electromechanical properties demonstrated by the Cu/PA 6 composite revealed its sensing capacity for a wide range of strains. Therefore, the composite yarn was affixed to the different regions of the human body and was capable of successfully monitoring various human motions, including finger bending, wrist bending, knee bending, drinking, and writing. In addition, rapid heat generation with high and uniform surface temperature (66.3 °C at 4.0 V in 45 s) validated the potential of the Cu/PA 6 yarn for wearable thermal heating devices. Moreover, rapid heating at a lower voltage, when attached to a wristband, revealed the capability of the composite yarn for localized heating or region-specific temperature regulation for personalized healthcare or comfort. This study informs a facile and effective strategy for developing robust yarn-shaped e-textiles for advanced wearable sensing and thermal heating.

Synthesis and characterization of tannic acid–copper complex: A promising anticholinesterase drug

This study aimed to present an optimized synthetic pathway for a complex formed between copper (II) metal ion and tannic acid (TA), which have a variety of pharmacological properties. The study also focused on characterizing this metallodrug, carrying out in vitro antioxidant and acetylcholinesterase enzyme (AChE) inhibition assays, and performing in vivo toxicity assay against zebrafish (Danio rerio), thus expanding the area of study involving syntheses of metal complexes to act as therapeutic agents. Through various characterization techniques, including UV–Vis Absorption Spectroscopy, Fourier Transform Infrared Spectroscopy (FTIR), Thermal Analysis (TG and DTG), 1H Nuclear Magnetic Resonance (1H NMR), Inductively Coupled Plasma with Optical Emission Spectrometry (ICP-OES), and Electron Paramagnetic Resonance (EPR), it was confirmed that the metal ion is coordinated to the ligand, exhibiting distorted planar square geometry with mononuclear copper (3.10 ± 0.10 % copper by ICP-OES). In vitro tests demonstrated that the TA–Cu complex presents antioxidant activity against DPPH (IC50 = 2.26 ± 0.01 µg mL−1) and ABTS (IC50 = 1.91 ± 0.07 µg mL−1) radical scavenging assays. These results were more promising than those obtained for the TA (4.25 ± 0.03 µg mL−1 and 3.37 ± 0.03 µg mL−1, respectively). In the in vitro inhibition of AChE assay, the TA–Cu complex (4.07 ± 0.04 µg mL−1) presented a lower IC50 value than TA (5.80 ± 0.09 µg mL−1), indicating that coordination to the metal center Cu (II) was able to improve the anticholinesterase activity of the free ligand. Furthermore, the TA–Cu complex did not show toxicity in the in vivo test with adult zebrafish for 96 h at the tested doses of 4–40 mg kg−1, with LD50 >40 mg kg−1. Thus, it is estimated that the TA–Cu complex is a metallodrug with anticholinesterase potential, representing a promising strategy for conducting future pre-clinical studies in models of Alzheimer’s disease.

Synthesis of innovative Daphne mucronata extract/Cu-MOF/PVA-PVP nanofiber as high-performance anticancer and antimicrobial agent

Nanofibers’ unique physical properties include mechanical strength, compressive strength, and high specific surface area, making them highly valuable and significant. Nanofiber can be containing nano compounds such as metal nano oxides, metal–organic framework, etc., as well as plant extracts. Plant extracts have had a special place in human life since the past and used in traditional medicine. The synthesis of new nanofibers containing plant extracts and metal–organic framework was the idea that we focused on it. For this purpose, Daphne mucronata extract and copper metal–organic framework, considering the high biological properties were used. For the synthesis of Daphne mucronata extract/Cu-MOF/PVA-PVP nanofiber, electrospinning method and polyvinyl alcohol (PVA) and polyvinyl pyrrolidone (PVP) were used. The final product’s structure was examined and verified using XRD (X-Ray diffraction analysis), EDAX (Energy dispersive X-ray analysis), CHNO EA (Carbon, hydrogen, nitrogen, and oxygen elemental analysis), SEM (Scanning electron microscope images), BET (Brunauer-Emmett-Teller theory), FT-IR (Fourier transform infrared spectroscopy), contact angle (Hydrophilic properties), mechanical strength and compressive strength. The specific surface area of the synthesized nanofiber and the diameter size of the synthesized particles were observed to be area 1102 m2/g and 80 nm, respectively. High hydrophilic properties (29°), high flexural strength (17.3 N/mm2), and high compressive strength (65.7 N/mm2) were among other characteristics of the synthesized nanofiber. Biological properties of the synthesized nanoparticle, such as anti-skin cancer, anti-bacterial, and anti-fungal properties, were tested. In the anticancer study, IC50 was 21 μg/mL, and in the antimicrobial studies (antibacterial and antifungal activity), the MIC was between 2 μg/mL and 64 μg/mL. Thus, the synthesized nanofiber can be incorporated as a bioactive compound in the medical industry, such as being utilized as bioactive medical bandages after other tests have been completed.