Pd Ions Research Articles

Robust free-base and metalated corrole radicals with reduction-induced emission

Preparing free-base porphyrinoid radicals that can function as coordination ligands is a challenging task. Here we report the synthesis of a stable, free-base benzocorrole (BC) radical containing only two inner NH protons via a retro-Diels-Alder conversion. The radical character of BC was fully supported by crystallographic analysis, spectroscopic evidence, and theoretical calculations. This neutral radical ligand allowed easy insertion of Zn(II), Ga(III), and Pd(II) ions to produce radical complexes. All these radicals exhibited luminescence-on responses under weak reducing atmosphere, corresponding to the conversion to their aromatic anions. The red fluorescence was observed for BC and its Zn(II) and Ga(III) complexes, and the near-infrared phosphorescence (> 900 nm) was detected for Pd(II) complex at room temperature. Furthermore, Ga(III) corrole exhibited a variation in fluorescence in response to axial coordination. Our findings provide a promising radical platform for coordination and developing novel functional materials with switchable spin and emission.

Pd-intercalated black phosphorus: An efficient electrocatalyst for CO2 reduction.

Nanoconfined catalysts enhance stabilization of reaction intermediates, facilitate electron transfer, and safeguard active centers, leading to superior electrocatalytic activity, particularly in CO2 reduction reactions (CO2RR). Despite their effectiveness, crafting nanoconfined catalysts is challenging due to unclear formation mechanisms. In this study, we introduce an electrochemical method to grow Pd clusters within the interlayers of two-dimensional black phosphorus, creating Pd cluster-intercalated black phosphorus (Pd-i-BP) as an electrocatalyst. Using in situ electrochemical liquid phase transmission electron microscopy (EC-TEM), we revealed the synthesis mechanism of Pd-i-BP, involving electrochemically driven Pd ion intercalation followed by reduction within the BP layers. The Pd-i-BP electrocatalyst exhibits exemplary CO2-to-formate conversion, achieving 90% Faradaic efficiency for formate production, owing to its distinct nanoconfined structure that stabilizes intermediates and enhances electron transfer. Density functional theory (DFT) calculations underscore the structural benefits for enhancing intermediate adsorption and catalyzing the reaction. Our insights deepen understanding of nanoconfined material synthesis, promising advanced, high-efficiency catalysts.

Enhanced optical and antimicrobial activities of mono Zn and bimetallic (Zn, Co), (Zn, Pd) ions modified MCM-41: structural and morphological investigation

Mono and bimetallic modified MCM-41(Mobil Composition of Matter No. 41): Zn-MCM (ZM), Zn/Co-MCM41 (ZCM), and Zn/Pd-MCM-41 (ZPM) molecular sieves were produced by a surfactant-assisted technique. The structural and textural features were examined through spectroscopic and analytical techniques. The XRD analysis indicated broadening of diffraction peaks and a shift towards higher 2-theta values in the metal-incorporated (M-MCM-41) samples, confirming the successful integration of metal atoms into the MCM-41 framework; it also highlighted the preservation of a hexagonal structure with reasonable regularity, emphasizing the influence of metal incorporation on the mesoporous architecture of MCM-41. N2 adsorption–desorption isotherms revealed type IV isotherms for all samples; the BET specific surface area decreased to 672.48, 667.90, and 562.50 m2/g in ZM, ZCM, and ZPM, respectively comparing to the unincorporated MCM-41 sample (1200 m2/g), indicating partial filling of mesopores by metal centers, as confirmed by TEM images. The diffuse reflectance spectra exhibited a noteworthy optical band gap reduction of MCM-41 (5.98 eV) upon the incorporation of Zn and Co/Zn ions, resulting in values of 5.86 and 5.24 eV, respectively, with refractive index values close to 2. Additional absorption bands energies are observed at 3.14, 3.18, and 1.70 eV in ZM, ZPM, and ZCM samples, respectively suggesting the suitability of the metal incorporated samples for the photocatalytic applications. The M-incorporated samples exhibited a decline in the transmission intensity accompanied by small shifts. The enhanced antimicrobial activity of the metal-incorporated samples, surpassing that of the pure MCM-41 against a variety of tested microorganisms, is attributed to the presence of incorporated metal species, which create a more acidic environment and substantially contribute to the heightened antimicrobial effectiveness. The ZM compound demonstrated potent inhibition against Bacillus cereus and Pseudomonas aeruginosa bacteria, displaying comparable efficacy to Ampicillin, as a reference antibiotic. Additionally, ZPM exhibited considerable inhibitory activity against Escherichia coli, surpassing the reference antibiotic and showing similar effectiveness against Bacillus cereus, Pseudomonas aeruginosa, and Salmonella typhimurium.

Pd(II) coordination molecule modified g-C3N4 for boosting photocatalytic hydrogen production

The photocatalytic H2 production activity of polymer carbon nitride (g-C3N4) is limited by the rapid recombination of photoelectron-hole pairs and slow surface reduction dynamic process. Here, a supramolecular complex (named R-TAP-Pd(II)) was fabricated via self-assembly of (R)-N-(1-phenylethyl)-4-(4-(pyridin-2-yl)-1H-1,2,3-triazol-1-yl)benzamide (R-TAP) with Pd(II) and used to modify g-C3N4. In the R-TAP-Pd(II)@g-C3N4 composite photocatalyst, the spin polarization of R-TAP-Pd(II) can promote charge transfer and inhibit photogenerated carrier recombination, as confirmed by spectral tests and photoelectrochemical performance tests. Electrochemical tests and in situ X-ray photoelectron spectroscopy (XPS) tests proved that the Pd(II) ion in the R-TAP-Pd(II) molecule can serve as active sites to accelerate H2 production. The R-TAP-Pd(II)@g-C3N4 presented a photocatalytic H2 generation rate of 1085 μmol g−1 h−1 when exposed to visible light, which was a about 278-fold increase compared with g-C3N4. This work finds a new approach to boost the photocatalytic efficiency of g-C3N4 via supramolecular self-assembly.

Novel self‐doped Pd/Cu bimetals in CMC/PANI composites: Efficient heterogeneous catalyst for cooperative Sonogashira and Sonogashira‐cyclization tandem reactions

A new Pd/Cu bimetal catalyst supported on carboxymethylcellulose/polyaniline (CMC/PANI) composites (Pd/Cu@CMC/PANI) was fabricated to investigate the cooperative effect between Pd/Cu bimetals in Sonogashira reactions. This approach involves the self‐organization of aniline on CMC via H‐bond, enabling in situ oxidative polymerization using Pd(II) and Cu(II) ions as co‐oxidants. Subsequently, Pd and Cu are self‐deposited on the resulting CMC/PANI composites through the interaction of coordination and metathesis. The morphological and compositional analysis of the prepared catalyst was performed using various analytical tools such as ICP‐AES, FT‐IR, XPS, SEM, TEM, EDS, elemental mapping, and TGA. The Pd/Cu@CMC/PANI composite as a cooperative catalyst for the Sonogashira couplings exhibited high catalytic activity with relatively low Pd loading over its monometallic Pd counterpart, demonstrating the cooperative effect between Pd and Cu. Then, this bimetallic catalyst was successfully adapted for Sonogashira‐cyclization tandem reaction for the synthesis of benzofuran with excellent yields. Significantly, the Pd/Cu@CMC/PANI catalyst exhibited thermal stability under the reaction conditions and could be easily retrieved and reused repeatedly for five runs in the model reaction without significant discernible performance degradation.

Amine-rich cyclotriphosphazene (P3N3) nano-cages for enhanced and selective Au(III) and Pd(II) recovery and hydrogen generation: Waste-to-resource tactics

Designing a new material for precious metals (PMs) recovery is of ultimate significance in the quest to explore highly efficient, selective, and stable adsorbents for a sustainable economy and green environment. Herein, novel amine-rich cyclotriphosphazene poly(tetrakis(4-aminophenyl)methane-co-cylotriphosphazene)- porous nano-cages (PTC-PNC) and microspheres (PTC-MS) were synthesized for adsorption and selective recovery of Au(III) and Pd(II) in aqueous solution. A combination of the abundant amine groups and the cage-like porous morphology of PTC-PNC makes it an ideal absorbent for recovery of the Au(III) (1592 mg g−1, pH 1.0, 60 oC) and Pd(II) (1372 mg g−1, pH 1.0, 60 oC) with high selectivity which was slightly decreased up to 8-11% even in the presence of 13 co-existing metals ions while an ultra-high recovery of 99% was obtained. The unique cage-like morphology of the PTC-PNC guarantees a fast adsorption equilibrium while the adsorption isotherm specifies a pseudo-second-order kinetic behavior and Langmuir isotherm. Amine groups were the most energetically favorable sites for the capturing and chelating of Au(III) and Pd(II) ions followed by their partial reduction to Au0 and Pd0. X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and high-resolution transmission electron spectroscopy (HRTEM) analysis were employed to explore interactions and reduction mechanisms during the adsorption process. Adopting the waste-to-resource approach, after Au(III) and Pd(II) recovery, these adsorbents were applied for catalytic hydrogen generation from ammonia borane (AB) hydrolysis. Due to its favorable electronic structure, the PTC-PNC@Pd exhibited a higher hydrogen generation than PTC-PNC@Au. The as-synthesized PTC-PNC could be employed as a promising material for other MPs' selective recovery and green energy generation applications.

Silica@poly(chitosan-N-isopropylacrylamide-methacrylic acid) microgels: Extraction of palladium (II) ions and in situ formation of palladium nanoparticles for pollutant reduction

Most of the transition metal ions and organic dyes are toxic in nature. Therefore, their removal from water is imperative for human health. For this purpose, various types of systems have been developed to tackle either transition metal ions or organic dyes individually. A core-shell microgel system is introduced which is capable of effectively removing both types (toxic organic dyes and transition metal ions) of pollutants. A long-rod-shaped silica@poly(chitosan-N-isopropylacrylamide-methacrylic acid) S@P(CS-NIPAM-MAA) S@P(CNM) core-shell microgel system was developed by free radical precipitation polymerization method (FRPPM). S@P(CNM) was utilized as an adsorbent for extracting palladium (II) (Pd (II)) ions from water under different concentrations of S@P(CNM), several agitation times, palladium (II) ion content, and pH levels. The adsorption data of Pd (II) ions on S@P(CNM) was evaluated by various adsorption isotherms. The kinetic study was investigated by employing pseudo-2nd order (Ps2O), Elovich model (ElM), intra-particle diffusion (IPDM), and pseudo-1st order (Ps1O). Additionally, palladium nanoparticles (Pd NPs) were generated via in-situ reduction of adsorbed Pd (II) ions within the P(CNM) shell region of S@P(CNM). The resulting Pd NPs loaded S@P(CNM) exhibited the capability to reduce organic pollutants like methyl orange (MeO), 4-nitrophenol (4NiP), methylene blue (MeB), and Rhodamine B (RhB) from aqueous medium. 0.766 min−1, 0.433 min−1, 0.682 min−1, and 1.140 min−1 were the values of pseudo 1st order rate constant (kobs) for catalytic reduction of MeB, 4NiP, MeO, and RhB respectively. The S@Pd-P(CNM) system exhibits significant catalytic potential for various organic transformations.

Construction of multi(iron)porphyrin array multilayers on quartz surface as peroxidase mimetics for H2O2 and glucose colorimetric, fluorometric and color-read detection

Multi(metallo)porphyrin arrays are important artificial biomimetics for mimicking the biological catalytic reactions in nature. Here, we report construction of multi(iron)porphyrin array ultrathin films on the quartz surface by coordination-driven layer-by-layer (LBL) assembling method with the Pd(II) ion as a connector and iron(III) tetrapyridylporphyrin (FeTPyP) as a linker. It is revealed that the (Pd-FeTPyP)n LBL multilayers can catalyze oxidation of 3,3′,5,5′-tetramethylbenzidine (TMB) in the presence of H2O2 with peroxidase-like activity, resulting in the formation of the blue-colored oxidized TMB (oxTMB). Coupled with glucose oxidase, three sensitive probes based on the colorimetric, fluorometric and color-read methods have been developed by using modified quartz plates as the heterogenous catalyst, with a glucose detection limit of about 0.89, 1.5 and 0.65 μM, respectively. Mechanism studies confirm an enhanced affinity between (Pd-FeTPyP)n and H2O2/TMB molecules and an improved catalytic performance, which are attributed to the reason that the FeTPyP macrocycles are well-dispersed and arranged on the two-dimensional quartz surface. Furthermore, owing to chemically anchored on the transparent quartz surface, the (Pd-FeTPyP)n films exhibit good stability with naked-eye observation of color change under moderate conditions, thus providing a potential candidate for developing colorimetric, fluorometric and color-read glucose biosensors.

Photo-catalytic dye degradation potentials of Ag-Pd bimetallic nanoparticles synthesized from Vitex negundo.

Plant extracts are a great alternative to synthesizing nanoparticles of different metals and metal oxides. This green synthesis method has opened up numerous possibilities in various scientific domains. In present study, Leaf extract from Vitex negundo is a non-deciduous, long-lasting shrub from the Verbenaceae family is used as capping and reducing agents for the synthesis of silver and palladium nanoparticles. The characterization study UV-vis spectrophotometer analysis showed absorbance value around 320nm which confirming that Ag-Pd nanoparticles have been successfully obtained. Further, SEM is used to investigate the morphology of Ag-Pd NPs, which revealing their spherical and rod-like configuration, aggregation, and the size of the particles are obtained between 50 and 100nm. The successful synthesis of Ag-Pd NPs was further confirmed by the EDAX chart, which displayed the peak of Ag and Pd at bending energies between 0.5 and 1.5keV. According to the quantitative study, Ag and Pd ions found about 5.24 and 13.28%, respectively. In addition, surface studies with TEM confirming that synthesized Ag-Pd NPs are predominates with spheres structure morphologies, with sizes averaging 11.20nm and ranging from 10 to 20nm. Further, Ag-Pd nanoparticles was applied as potential photocatalyst materials to degrade methylene blue dye and found about 85% of the degradation efficiency within 150min of the sunlight exposure thus could be used as catalyst to removal of hazardous organic dye molecules.

A review of hydrazide-hydrazone metal complexes’ antitumor potential

Cancer inflicts a tremendous burden on modern society, and more effective and selective treatments need to be developed. Metallodrugs have been extensively explored as alternatives to current chemotherapeutic regimens that suffer from shortcomings such as severe side effects and acquired resistance. Hydrazide-hydrazones are a family of organic molecules containing the hydrazone functionality attached to a carbonyl group (−C=N−NH−CO). These molecules are extremely versatile and can be obtained from modular reactions between hydrazides and aldehydes or ketones, of which a large library is commercially available. Hydrazide-hydrazones show numerous therapeutic effects, and typically, their metal complexes exhibit increased potency. This review aims to highlight the potential of hydrazide-hydrazone metal complexes in the field of anticancer research. It focuses on the literature published in the last 10 years (2013-2023) and describes their biological effects, their antiproliferative activity and their mechanisms of action. It is organized by metal ion, including Cu, Ru, Pt, Pd, V, other d-block, lanthanide, and Ga and Sn ions. It highlights the diversity of molecules being developed and can be used as a guide for developing new hydrazide–hydrazones as efficient anticancer agents.

Catalytically Active SiO2 Aerogels Comprising Chelate Complexes of Palladium.

A series of silica-based aerogels comprising novel bifunctional chelating ligands was prepared. To produce target aerogels, two aminosilanes, namely (3-aminopropyl)trimethoxysilane (APTMS) and N-(2-aminoethyl)-3-aminopropyltrimethoxysilane (AEAPTMS), were acylated by natural amino acids ((S)-(+)-2-phenylglycine or L-phenylalanine), followed by gelation and supercritical drying (SCD). Lithium tetrachloropalladate was used as the metal ion source to prepare strong complexes of Pd2+ with amino acids covalently bonded to a silica matrix. Aerogels bearing chelate complexes retain the Pd2+ oxidation state after supercritical drying in CO2, but the Pd ion is reduced to Pd metal after SCD in isopropanol. Depending on the structure of amino complexes, Pd-containing aerogels showed catalytic activity and selectivity in the hydrogenation reactions of C=C, C≡C and C=O bonds.

Self-assembly of two pairs of homochiral M2L4 coordination capsules with varied confined space using Tröger's base ligands

Chiral coordination molecular cages/capsules with discrete nanoconfined chiral cavities demonstrate significant potential applications across various fields. In this study, we utilized Tröger's base as the building block to design and synthesize two pairs of enantiopure ligands. These ligands were then self-assembled with Pd(II) ions through chiral self-sorting coordination, resulting in the formation of two pairs of homochiral M2L4-type coordination molecular capsules. Notably, due to differences in the substitution positions on the Tröger's base, these two pairs of enantiomeric coordination molecular capsules exhibited distinct levels of cavity closures, cavity sizes, and host-guest recognition properties. This research offers valuable insights into the construction of novel chiral molecular capsules and the regulation of confined cavities.

Silver nanoprism-mediated colourimetric sensing probe for efficient detection of Pd(II) and Pt(II) ions in water and reuse of formed bimetallic nanoprisms

Sensitive and selective methods for detecting Pd(II) and Pt(II) ions in water are crucial for environmental monitoring and remediation. Although traditional methods for detection of Pd(II) and Pt(II) ions are accurate and sensitive, they face substantial challenges due to high costs, reliance on specialised equipment and limited field applicability, thereby presenting notable limitations. In this study, we introduce a novel colourimetric sensing probe designed specifically to identify Pd(II) and Pt(II) ions in aqueous solutions. This probe utilises the enhanced chemical stability of Ag nanoprisms achieved through Pd or Pt deposition on their surfaces. Our approach features exceptionally low limits of detection of 2.6 nM for Pd(II) and 0.3 nM for Pt(II), indicating an impressive detection range. Furthermore, the probe’s ease of use, cost-effectiveness and compatibility with both naked eye and UV–Vis spectrophotometric detection make it a selective, reliable and affordable option for point-of-care analysis. Beyond its impressive sensitivity for ion detection, this methodology offers the additional benefit of enabling the on-demand synthesis of customised bimetallic catalysts. The synthesised Ag/Pd and Ag/Pt bimetallic nanoprisms demonstrate promising catalytic potential for environmental remediation. This advancement paves the way for efficient recycling and reuse of valuable Pd(II) and Pt(II) ions in various catalytic applications.

Acid-resisting covalent organic framework enabling high-efficiency palladium recovery from used palladium catalyst under strong acid

Pd recovery from used sources is now receiving growing attentions, due to its scarcity and important application in many fields, however, which is still seriously restricted by the lack available adsorbent that can effectively capture palladium (Pd) from strong acid (>3 M). To this end, we report herein an acid-resisting covalent organic framework (COF), namely ECUT-COF-20, for such use. This new adsorbent is found to perform a benchmark Pd recovery performance from 6 M acidity such as the fast adsorption kinetics (1 min) and high uptake capacity (181 mg/g). The breakthrough test from a Pd/C-digested solution is used to confirm its practical application, giving an exceptionally one-round 95 % Pd recovery efficiency. The mechanism, as unveiled by characterization and DFT calculation, is due to a spatial and functional separation in this adsorbent, which could consequently not only overcome the influence of strong acid, but also provide abundant hydrogen bonds for fixing Pd ions.

The Pd (II) Reduction Mechanisms in Bacillus megaterium Y-4 Revealed by Proteomic Analysis.

Many studies have been conducted on the microbial reduction of Pd (II) to palladium nanoparticles (Pd-NPs) due to the environmental friendliness, low cost, and the decreased toxicity of Pd (II) ions. In this study, we investigate the reduction mechanism of Pd (II) by Bacillus megaterium Y-4 through proteomics. The data are available via ProteomeXchange with identifier PXD049711. Our results revealed that B. megaterium Y-4 may use the endogenous electron donor (NAD(P)H) generated by nirB, tdh, and fabG and reductase to reduce Pd (II) to Pd-NPs. The expression levels of fabG, tdh, gudB, and rocG that generate NAD(P)H were further increased, and the number of reduced Pd-NPs was further increased with the exogenous electron donor sodium formate. Endogenous electron mediators such as quinones and flavins in B. megaterium Y-4 can further enhance Pd (II) reduction. The findings provided invaluable information regarding the reduction mechanism of Pd (II) by B. megaterium Y-4 at the proteome level.

Synthesis and Application of 3-[3-Phenylpyrazylazo]-2,7-Naphthalendiol for Improved Palladium Determination in Environmental Samples and Enhanced ZnO Nanoparticle Performance

In this study, a spectrophotometric method for the determination of low levels of palladium (II) was developed by forming a complex with the new reagent 3-(3-phenyl pyrazyl azo)-2,7-naphthalendiol (3PPAN). The complex showed maximum absorption at 612 nm with a maximum molar absorptivity of 4.911?104 L/mol/cm, and a linear correlation was established between absorbance and concentration. The accuracy and repeatability of the method were evaluated and found to be precise (RSD 1.22%) and accurate (relative error 0.157%). The method?s selectivity was also tested by evaluating the effect of various ions. The stability constant of the complex was determined to be 2.759?107 L/mol. The method was successfully applied to the determination of Pd (II) ions in environmental samples of water and soil. In addition, the new ligand (3PPAN) was used to improve the properties of nano ZnO through a ligand exchange reaction on nanoparticles.. KEYWORDS :Azo, Palladium, Spectrophotometric, ZnO nanoparticles.

Indium nanocubes based recyclable fluorescent chemosensor for sustainable environmental monitoring: pH-induced fluorescence transition and selective detection of Pd(II) ions

Rapid modern industrialization and urbanization have escalated heavy metal pollution, with palladium (Pd2+) raising significant concerns due to its extensive usage in catalysis, hydrogen storage, and electronics, thereby imposing substantial risks on the environment and human health. In this study, we report a highly fluorescent indium nanocubes based chemosensor (InNCs) functionalized with perylene tetracarboxylic acid (PTCA) and 4-(pyridyl)ethenyl benzene (PEB). The InNCs exhibited emission maximum at 415 nm (λex ∼ 350 nm) with robust chemical and photo-stability, and acted as a fluorogenic probe for selective recognition of Pd2+ in aqueous medium. The fluorescence sensing properties of InNCs were thoroughly assessed via different techniques including steady-state absorption, emission and time-resolved emission spectroscopic methods. Among the various competitive analytes, only Pd2+ could induce a significant fluorescence quenching in the probe. This “turn-off” fluorescence sensing demonstrated a remarkably low LoD of ∼65 nM. Notably, with the addition of EDTA, the probe displayed good recyclability upto 4 cycles. The sensory probe was successfully employed as a reusable platform to estimate Pd(II) in different real water and soil samples with considerable accuracy (∼ 5–10 % error). Moreover, the probe exhibited a pH-induced fluorescence transition, indicating its potential to be applied as a pH sensor. The Pd(II) binding and pH-sensing mechanisms have also been elucidated through density functional theory (DFT) calculations.

Palladium and platinum complexes based on pyridine bases induced anticancer effectiveness via apoptosis protein signaling in cancer cells.

Palladium and platinum complexes, especially those that include cisplatin, can be useful chemotherapeutic drugs. Alternatives that have less adverse effects and require lower dosages of treatment could be provided by complexes containing pyridine bases. The complexes [Pd(SCN)2(4-Acpy)2] (1), [Pd(N3)2(4-Acpy)2] (2) [Pd(paOH)2].2Cl (3) and [Pt(SCN)2(paO)2] (4) were prepared by self-assembly method at ambient temperature; (4-Acpy = 4-acetylpyridine and paOH = pyridine-2-carbaldehyde-oxime). The structure of complexes 1-4 was confirmed using spectroscopic and X-ray crystallography methods. Complexes1-4 have similar features in isomerism that include the trans coordination geometry of pyridine ligands with Pd or Pt ion. The 3D network structure of complexes 1-4 was constructed by an infinite number of discrete mononuclear molecules extending via H-bonds. The Pd and Pt complexes1-4with pyridine ligands were assessed on MCF-7, T47D breast cancer cells and HCT116 colon cancer cells. The study evaluated cell death through apoptosis and cell cycle phases in MCF-7 cells treated with palladium or platinum conjugated with pyridine base. Upon treatment of MCF-7 with these complexes, the expression of apoptotic signals (Bcl2, p53, Bax and c-Myc) and cell cycle signals (p16, CDK1A, CDK1B) were evaluated. Compared to other complexes and cisplatin, IC50 of complex 1 was lowest in MCF-7 cells and complex 2 in T47D cells. Complex 4 has the highest effectiveness on HCT116. The selective index (SI) of complexes 1-4 has a value of more than two for all cancer cell lines, indicating that the complexes were less toxic to normal cells when given the same dose. MCF-7 cells treated with complex 2 and platinum complex 4 exhibited the highest level of early apoptosis. p16 may be signal arrest cells in Sub G, which was observed in cells treated with palladium complexes that suppress excessive cell proliferation. High c-Myc expression of treated cells with four complexes 1-4 and cisplatin could induce p53. All complexes 1-4 elevated the expression of Bax and triggered by the tumor suppressor gene p53. p53 was downregulating the expression of Bcl2.

Rapid separation of the low concentration Pd from Pd-Pt coexisting systems: Cyano-group’s monomer-specific affinity

Rapid separation of low concentration palladium (Pd) from Pd-Platinum (Pt) coexisting systems remains a formidable challenge, primarily due to the undifferentiated substitution of ligands in Pd/Pt complexes by adsorption sites. The development of an adsorbent featuring monomer-specific affinity adsorption sites for Pd/Pt could mitigate this drawback. Herein, Manganese hexacyanoferrate (MnHCF) possessing the sensitivity and specificity to Pd ions (Pd(II)) was synthesized via the facile co-precipitation method. MnHCF could rapidly and selectively capture 90.30 % of Pd(II) from a 10 ppm Pd-Pt coexisting system within just 5 min. Spectroscopic analyses and density functional theory (DFT) calculations indicated that cyano-group (CN) in MnHCF exhibited the monomer-specific affinity for targeted capturing Pd via the direct and strong coordination interaction (Fe-CN-PdCl2), which was co-determined by the electron-losing of C (0.06 e) and N (0.07 e) atom. At the same time, CN could neither react directly with the fully coordinated [PtCl6]2− species nor substitute the Cl− ligand, both of which contributed to the non-adsorption of Pt, thus triggering the Pd-Pt separation. This study provides a promising candidate adsorbent for practical applications in platinum group metals recovery by the design of adsorption sites with monomer-specific affinity.

Synthesis, characterization, PXRD studies, and theoretical calculation of the effect of gamma irradiation and antimicrobial studies on novel Pd(II), Cu(II), and Cu(I) complexes.

The main objective of this study is to synthesize and characterize of a new three complexes of Pd (II), Cu (II), and Cu (I) metal ions with novel ligand ((Z)-2-(phenylamino)-N'-(thiophen-2-ylmethylene)acetohydrazide) H2LB. The structural composition of new compounds was assessed using several analytical techniques including FT-IR, 1H-NMR, electronic spectra, powder X-ray diffraction, and thermal behavior analysis. The Gaussian09 program employed the Density Functional Theory (DFT) approach to optimize the geometry of all synthesized compounds, therefore obtaining the most favorable structures and crucial parameters. An investigation was conducted to examine the impact of γ-irradiation on ligands and complexes. Before and after γ-irradiation, the antimicrobial efficiency was investigated for the activity of ligands and their chelates. The Cu(I) complex demonstrated enhanced antibacterial activity after irradiation, as well as other standard medications such as ampicillin and gentamicin. Similarly, the Cu(I) complex exhibited superior activity against antifungal species relative to the standard drug Nystatin. The docking investigation utilized the target location of the topoisomerase enzyme (2xct) chain A.