Tunable Afterglow and Self-Trapped Exciton Emissions in Zr (IV)-Based Organic-Inorganic Metal Halide Hybrids by Metal-Ion Doping.

Low-dimensional hybrid metal halide (LDHMH) materials have attracted considerable attention owing to their intriguing optical properties. To the best of the knowledge, this is the first study to successfully demonstrate both self-trap exciton (STE) and afterglow emissions in Zr-based LDHMH materials. The obtained pure (Ph3 S)2 ZrCl6 crystals showed near-ultraviolet phosphorescence and a green afterglow owing to the organic cation Ph3 S+ , while the Bi-doped and Sb-doped crystals exhibited both STE and afterglow emissions. However, the Te-doped crystals showed only a broad yellow STE emission owing to the [TeCl6 ]2- octahedron. In addition, all the crystals showed good stability. Notably, Sb-doped crystals produced white light, which can be adjusted between cold white and warm white using different excitations. Finally, this strategy for both STE and afterglow emissions can be applied to other LDHMH materials for optical applications.

In situ growth of Zr-based metal-organic framework UiO-66-NH2 for open-tubular capillary electrochromatography.

The high stability and other properties of Zr(IV)-based metal organic frameworks(MOFs) make it a promising choice for chromatographic separation, while the application in open-tubular capillary electrochromatography (OT-CEC) separation has not been explored yet. Herein, we report the first example of the in-situ growth of UiO-66-NH2 onto the capillary for open-tubular capillary electrochromatography. UiO-66-NH2 consists of ZrCl4 and 2-amino-1,4-benzenedicarboxylic acid, which is highly porous and stable in a variety of solvents. The prepared UiO-66-NH2 modified capillary was characterized by scanning electron microscopy (SEM) and Fourier transform infrared spectra (FT-IR), and the results confirmed the successful growth of the UiO-66-NH2 . The baseline separation of chlorobenzenes, phenoxyacids and two groups of phenols was achieved owing to the combined interaction of π-π interaction, hydrophobic interaction, molecular sieve effect, electrophoretic migration and hydrogen-bonding interaction etc. Besides, the prepared capillaries showed good reproducibility, with relative standard deviations (RSDs) for intra-day, inter-day and column-to-column runs in the range of 1.38-2.60%, 3.39-4.05%, and 3.47-5.03%, respectively. Our work indicates Zr(IV)-based MOFs are promising materials as stationary phase in CEC separation.

Highly Stable Zr(IV)-Based Porphyrinic Metal-Organic Frameworks as an Adsorbent for the Effective Removal of Gatifloxacin from Aqueous Solution.

Water stable Zr-metal−organic framework nanoparticles (PCN-224 NPs, PCN refers to porous coordination network) have been solvothermally synthesized. PCN-224 NPs show spherical shape with smooth surface and particle size of approximately 200 nm. PCN-224 NPs can be stable in acid and aqueous solutions, as confirmed by powder X-ray diffraction. Gatifloxacin (GTF) adsorption measurements showed that PCN-224 NPs exhibit a high adsorption capacity of 876 mg·g−1. Meanwhile, the adsorption factors, adsorption characteristics, and mechanisms of GTF were investigated in batch adsorption experiments.

Silica-gel Particles Loaded with an Ionic Liquid for Separation of Zr(IV) Prior to Its Determination by ICP-OES.

A new ionic liquid loaded silica gel amine (SG-APTMS-N,N-EPANTf2) was developed, as an adsorptive material, for selective adsorption and determination of zirconium, Zr(IV), without the need for a chelating intermediate. Based on a selectivity study, the SG-APTMS-N,N-EPANTf2 phase showed a perfect selectivity towards Zr(IV) at pH 4 as compared to other metallic ions, including gold [Au(III)], copper [Cu(II)], cobalt [Co(II)], chromium [Cr(III)], lead [Pb(II)], selenium [Se(IV)] and mercury [Hg(II)] ions. The influence of pH, Zr(IV) concentration, contact time and interfering ions on SG-APTMS-N,N-EPANTf2 uptake for Zr(IV) was evaluated. The presence of incorporated donor atoms in newly synthesized SG-APTMS-N,N-EPANTf2 phase played a significant role in enhancing its uptake capacity of Zr(IV) by 78.64% in contrast to silica gel (activated). The equilibrium and kinetic information of Zr(IV) adsorption onto SG-APTMS-N,N-EPANTf2 were best expressed by Langmuir and pseudo second-order kinetic models, respectively. General co-existing cations did not interfere with the extraction and detection of Zr(IV). Finally, the analytical efficiency of the newly developed method was also confirmed by implementing it for the determination of Zr(IV) in several water samples.

Synthesis, characterization and As(III) scavenging behaviours of mango peel waste loaded with Zr(IV) ion from contaminated water.

Raw mango peel (RMP) was first saponified to yield saponified mango peel (SMP), which was then loaded with Zr(IV) ions to form a biosorbent for As(III) scavenging.The biosorption behaviors and mechanisms of As(III) scavenging using RMP and Zr(IV)-loaded saponified mango peel (Zr(IV)-SMP) were investigated batchwise. The As(III) scavenging efficiency of RMP increased from 20.13 % to 87.32 % after Zr(IV) loading. Optimum contact time of 6 h has been investigated for As(III) scavenging by Zr(IV)-SMP, and the data on kinetics is well fitted to the pseudo-second-order (PSO) model. Similarly, isotherm data of Zr(IV)-SMP fitted well to the Langmuir isotherm model with the maximum As(III) scavenging potential of 45.52 mg/g. Chloride (Cl-) and nitrate (NO3 -) have negligible influence on As(III) scavenging, but sulphate (SO4 2-) interferes significantly. The exhausted Zr(IV)-SMP could be easily regenerated by treating with 2MNaOH. A mechanistic study indicates that As(III) scavenging is primarily contributed to electrostatic interaction and ligand exchange, which is confirmed from both instrumental and chemical characterizations techniques. Tubewell underground water polluted with a trace amount of arsenic (98.63 µg/L) could be successfully lowered down to the WHO standard (10 µg/L) by applying a small amount of Zr(IV)-SMP. Therefore, the Zr(IV)-SMP investigated in this work can be a low-cost, environmentally benign, and promising alternative for scavenging trace levels of arsenic from contaminated water.

Rapid visual dual-mode detection of Zr(IV) based on L-histidine functionalized gold nanoparticles.

Heavy metal pollution has always been a great threat to human health and safety. Compared with other heavy metals, although zirconium ion (Zr(IV)) is equally harmful, due to the lack of research on Zr(IV) in the biological systems and environment, its detection does not seem to have received the attention it deserves. Herein, a rapid visual dual-mode detection (colorimetric and chrominance method) of Zr(IV) based on L-histidine functionalized gold nanoparticles (HIS-AuNPs) has been reported. AuNPs and HIS-AuNPs before and after adding Zr(IV) were characterized by UV-Vis, TEM, DLS, Zeta potential, EDS and FT-IR, etc. These results showed that L-histidine was successfully modified on the surface of AuNPs by forming a stable Au-N bond, and its modification had little effect on the dispersion degree of AuNPs. After the addition of Zr(IV), interaction of this metal ion with the imidazolyl group on L-histidine can obviously cause the aggregation of HIS-AuNPs within 12 min, and the dispersion state and particle size of HIS-AuNPs can be significantly changed. These two detection modes were established by means of absorbance and color change of solution, and being used in addition and recovery experiments of Zr(IV) in natural water. Under the optimal conditions, these two modes exhibited good linearity within 15-70 and 20-100 µmol L-1, and limit of detection of 2.62 and 6.25 µmol L-1. The proposed method was highly sensitive and selective, which provided a new convenient way to realize the detection of Zr(IV).

A stable Zr(IV)-MOF for efficient removal of trace SO2 from flue gas in dry and humid conditions.

Obtaining suitable adsorbents for selective separation of SO2 from flue gas still remains an important issue. A stable Zr(IV)-MOF (Zr-PTBA) can be conveniently synthesized through the self-assembly of a tetracarboxylic acid ligand (H4L = 4,4',4'',4'''-(1,4-phenylenebis(azanetriyl))tetrabenzoic acid) and ZrCl4 in the presence of trace water. It exhibits a three-dimensional porous structure. The BET surface area is 1112.72 m2/g and the average pore size distribution focus on 5.9, 8.0 and 9.3 Å. Interestingly, Zr-PTBA shows selective adsorption of SO2. The maximum uptake reaches 223.21 cm3/g at ambient condition. While it exhibits lower adsorption uptake of CO2 (30.50 cm3/g) and hardly adsorbs O2 (2.57 cm3/g) and N2 (1.31 cm3/g). Higher IAST selectivities of SO2/CO2 (21.9), SO2/N2 (912.7), SO2/O2 (2269.9) and SO2/CH4 (85.0) have been obtained, which reveal its' excellent gas separation performance. Breakthrough experiment further confirms its application for flue gas deep desulfurization both in dry and humid conditions. Furthermore, the gas adsorption results and mechanisms have also been studied by theoretical calculations.

Evaluation of coumarin-tagged deferoxamine as a Zr(IV)-based PET/fluorescence dual imaging probe.

Desferoxamine (DFO) is currently the golden standard chelator for 89Zr4+, a promising nuclide for positron emission tomography imaging (PET). The natural siderophore DFO had previously been conjugated with fluorophores to obtain Fe(III) sensing molecules. In this study, a fluorescent coumarin derivative of DFO (DFOC) has been prepared and characterized (potentiometry, UV-Vis spectroscopy) for what concerns its protonation and metal coordination properties towards PET-relevant ions (Cu(II), Zr(IV)), evidencing strong similarity with pristine DFO. Retention of DFOC fluorescence emission upon metal binding has been checked (fluorescence spectrophotometry), as it would - and does - allow for optical (fluorescent) imaging, thus unlocking bimodal (PET/fluorescence) imaging for 89Zr(IV) tracers. Crystal violet and MTT assays on NIH-3 T3 fibroblasts and MDA-MB 231 mammary adenocarcinoma cell lines demonstrated, respectively, no cytotoxicity nor metabolic impairment at usual radiodiagnostic concentrations of ZrDFOC. Clonogenic colony-forming assay performed on X-irradiated MDA-MB 231 cells showed no interference of ZrDFOC with radiosensitivity. Morphological biodistribution (confocal fluorescence, transmission electron microscopy) assays on the same cells suggested internalization of the complex through endocytosis. Overall, these results support fluorophore-tagged DFO as a suitable option to achieve dual imaging (PET/fluorescence) probes based on 89Zr.

Single and selective transport of Zr(IV) ions with trioctyl amine dissolved in kerosene using a multidropped liquid membrane technique.

It is very important to develop a process for selectively extracting Zr(IV) ions from the solution medium to produce zirconium metal used in industry and nuclear reactors. In this study, the parameters affecting the extraction of Zr(IV) ions were investigated using a multidropped liquid membrane (MDLM) system. Trioctyl amine (TOA) dissolved in kerosene was used as a carrier ligand in the extraction of Zr(IV) ions by the MDLM technique. The effect of carrier concentration and stripping solution concentration, pH, and the temperature in the donor phase on the transport of Zr(IV) were investigated. The optimum condition for the transportation of Zr(IV) was a 0.50 M H2SO4 solution as donor phase, 0.10 molL-1 TOA as a carrier, and 0.10 M Na2CO3 as acceptor phase. The transport percentage of Zr(IV) was increased up to >99% and the calculated activation energy which is 6.36 kcal mol-1 indicated that the process was diffusion controlled by Zr(IV) ions. The results showed that the MDLM system, which resembles a bulky membrane system in shape, is a promising technique for the extraction of Zr(IV) ions from an acidic solution. It is more practical and effective than bulk, supported, or inclusion, and emulsion liquid membrane techniques.

In vitro DNA binding, pBR322 cleavage and molecular docking studies of 1,2-diaminobenzene, dichloro glycyl glycinate tin(IV) and zirconium(IV) complexes.

De novo design and synthesis of complexes 1,2-diaminobenzene, dichloro glycyl glycinate tin(IV) and zirconium(IV), 1 and 2 as molecular drug entities were carried out. The structure elucidation of 1 and 2 was done by analytical techniques and spectroscopic methods viz. IR, UV-vis, 1H, 13C, 119Sn NMR, ESI-Mass and XRD techniques. In vitro DNA binding studies of 1 and 2 by various biophysical techniques viz electronic absorption, emission spectroscopy and circular dichroism measurements were carried out to evaluate their potential to act as chemotherapeutic candidates; furthermore, cleavage studies with pBR322plasmid DNA and computer-aided molecular docking studies were also done to study the mechanistic pathway and mode of binding at the molecular level. The observed results revealed that complex 1 exhibited greater DNA binding propensity in contrast to complex 2 primarily via electrostatic binding mode. The pBR322 DNA cleavage studies of both the complexes revealed the hydrolytic cleavage mechanism and DNA minor groove binding, which was ascertained by molecular docking studies of the drug candidate. Communicated by Ramaswamy H. Sarma.

Removal of arsenate from contaminated waters by novel zirconium and zirconium-iron modified biochar.

A novel biochar metal oxide composite was synthesized for effective removal of arsenate (As(V)) from aqueous solution. The materials synthesized for As(V) removal was based on a biosolid-derived biochar (BSBC) impregnated with zirconium (Zr) and zirconium-iron (Zr-Fe). The synthesized materials were comprehensively characterized with a range of techniques including Brunauer-Emmett-Teller (BET-N2) surface area, zeta potential, Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). The results confirmed that loading of Zr and Zr-Fe onto the biochar surface was successful. The influence of pH, biochar density, ionic strength, As(V) dose rate, major anions and cations on As(V) removal was also investigated. Under all pH and reaction conditions the Zr-Fe composite biochar removed the greatest As(V) from solution of the materials tested. The maximum sorption capacity reached 15.2 mg/g for pristine BSBC (pH 4.0), while modified Zr-BSBC and Zr-FeBSBC composites achieved 33.1 and 62.5 mg/g (pH 6), respectively. The thermodynamic parameters (Gibbs free energy, enthalpy, and entropy) suggested that the adsorption process is spontaneous and endothermic. The ZrBSBC and Zr-FeBSBC showed excellent reusability and stability over four cycles. Unmodified biochar resulted in partial reduction of As(V) under oxic conditions, whilst modified biochars did not influence the oxidation state of As. All results demonstrated that the Zr and Zr-Fe BSBC composites could perform as promising adsorbents for efficient arsenate removal from natural waters.

Development of zirconium modified adenosine triphosphate functionalized monolith for specific enrichment of N-glycans.

In this study, to selectively enrich N-glycans from complex biological samples, a novel Zr(IV) modified adenosine triphosphate (Zr(IV)-ATP) functionalized monolith was prepared through a facile approach. Well-defined macroporous structure was observed in the ATP functionalized monolith, which allows rapid mass transfer under low backpressure and is beneficial for the enrichment of N-glycans. After being modified with Zr(IV), the resulting Zr(IV)-ATP functionalized monolith could selectively capture N-glycans through the specific interactions between the sulfonate groups of 1-aminopyrene-3,6,8-trisulfonic acid (APTS) labeled N-glycans and Zr(IV). An APTS labeled maltooligosaccharide ladder was used to optimize the enrichment conditions for APTS labeled N-glycans, and capillary electrophoresis (CE) coupled with laser-induced fluorescence (LIF) detector was employed to evaluate the enrichment efficiency. The results show that the APTS labeled maltooligosaccharides could be enriched under the selected conditions and the signal amplify factors of the maltooligosaccharides were between 7.4 and 19.5 with RSDs for reproducibility from 4.0% to 8.3% (n = 3). Finally, the proposed method was successfully used for the enrichment and detection of N-glycans released from Ribonuclease B.

Selective and efficient sequestration of phosphate from waters using reusable nano-Zr(IV) oxide impregnated agricultural residue anion exchanger.

There is an urgent need to develop low-cost and effective adsorbents for enhanced removal of phosphate from contaminated waters. In this study, nanosized Zr(IV) oxide particles were immobilized on the amino modified corn staw (MCS) to fabricate a novel nanocomposite (Zr@MCS) with superior application capability. Compared with the widely used commercial anion exchangers in previous studies, the modified agricultural residue was empolyed as the host to avoid the high costs and secondary pollution in the preparation. Zr@MCS displayed remarkable selective removal of phosphate from water even in the presence of coexisting anions (Cl-, SO42-, NO3-) at high levels, as well as with a high adsorption capacity, fast adsorption kinetics and high availability in the wide range of pH 2-8 toward phosphate. The excellent adsorption performance of Zr@MCS is attributed to the synergistic effect of the electrostatic attraction of the quaternary ammonium groups fixed on the host skeleton and the specific adsorption of phosphate derived from the hydroxyl functional groups of Zr(IV) oxide. The exhausted Zr@MCS can be effectively regenerated by 5% NaOH-NaCl solution for sustainably utilized, and phosphorus in the desorption effluent could be recovered as high-quality struvite by a simple struvite recovery process. Furthermore, the considerable treatment volume for the synthetic solution and real wastewater in a fixed-bed flow system indicated that Zr@MCS is of great potential for phosphate removal in practice.

Development of polyaminated chitosan-zirconium(IV) complex bead adsorbent for highly efficient removal and recovery of phosphorus in aqueous solutions.

The aim of this work is to examine the adsorption performance and mechanism of phosphorus (P) onto polyethyene polyamine (PEPA) grafted chitosan-zirconium(IV) composite beads (CS-Zr-PEPA) from aqueous solutions. The morphology, functional groups, and surface area of the CS-Zr-PEPA beads were characterized by SEM, FTIR, and BET analysis. Batch adsorption experiments were conducted via different operating parameters such as solution pH, initial phosphate concentration, co-existing anions and temperature. The adsorption kinetics, equilibrium isotherms and adsorption stability of the adsorbent were scrutinized. In comparison with other CS-based beads, the CS-Zr-PEPA had a greater affinity towards P and exhibited a maximum adsorption capacity of 103.96 mg-P/g predicted by Langmuir mode. The reusability studies of CS-Zr-PEPA beads were carried out. The CS-Zr-PEPA beads exhibit preferable sequestration of P through specific interactions, as further demonstrated by studying physicochemical characteristics of the virgin beads and P-adsorbed beads using X-ray photoelectron spectroscopy (XPS). The column performance of CS-Zr-PEPA beads was tested with P-containing wastewater. Results indicated that the developed CS-Zr-PEPA composite beads could be utilized as a promising adsorbent for effective removal and recovery of P from water and wastewater.

The solution thermodynamic stability of desferrioxamine B (DFO) with Zr(IV).

Desferrioxamine B (DFO, [H4L]+, ligand) is currently the preferred chelator for 89Zr(IV), however the biological studies suggest that it releases the metal ion in vivo. Herein, we present the solution thermodynamics of complexes formed between Zr(IV) and this hexadentate chelating agent, the data surprisingly not yet available in the literature. Several techniques including electrospray ionization mass spectrometry (ESI-MS), potentiometry, UV-Vis spectroscopy and isothermal titration calorimetry (ITC) were used to determine the stoichiometry and thermodynamic stability of complexes formed in solution over pH range 1-11, overcoming all the difficulties with the characterisation of the aqueous solution chemistry of Zr(IV) complexes, like strong hydrolysis and lack of spectral information. A model containing only mononuclear complexes, i.e. [ZrHL]2+ [ZrL]+, [ZrLH-1] throughout the entire measured pH range is proposed. The stability constants and pM (Zr(IV)) value determined for Zr(IV)-DFO system, place DFO among good Zr(IV) chelators, however the formation of 6-coordinate unsaturated complexes (i.e. with coordination sphere of 8-coordinate Zr(IV) completed by water molecules), together with the susceptibility of coordinated water molecule to deprotonation, are suggested to be the reason of in vivo instability of 89Zr(IV)-DFO complexes.

Tuning Water Sorption in Highly Stable Zr(IV)-Metal-Organic Frameworks through Local Functionalization of Metal Clusters.

Water adsorption of metal-organic frameworks (MOFs) is attracting intense interest because of their potential applications in atmospheric water harvesting, dehumidification, and adsorption-based heating and cooling. In this work, through using a hexacarboxylate ligand, four new isostructural Zr(IV)-MOFs (BUT-46F, -46A, -46W, and -46B) with rare low-symmetric 9-connected Zr6 clusters were synthesized and structurally characterized. These MOFs are highly stable in water, HCl aqueous solution (pH = 1), and NaOH aqueous solution (pH = 10) at room temperature, as well as in boiling water. Interestingly, the rational modification of the metal clusters in these MOFs with different functional groups (HCOO-, CH3COO-, H2O/OH, and PhCOO-) enables the precise tuning of their water adsorption properties, which is quite important for given application. Furthermore, all four MOFs show excellent regenerability under mild conditions and good cyclic performance in water adsorption.

Rationally Designed, "Stable-on-the-Table" NanoBiocatalysts Bound to Zr(IV) Phosphate Nanosheets.

Rational approaches for the control of nano-bio interfaces for enzyme stabilization are vital for engineering advanced, functional nanobiocatalysts, biosensors, implants, or "smart" drug delivery systems. This chapter presents an overview of our recent efforts on structural, functional, and mechanistic details of enzyme nanomaterials design, and describes how progress is being made by hypothesis-driven rational approaches. Interactions of a number of enzymes having wide ranges of surface charges, sizes, and functional groups with α-Zr(IV)phosphate (α-ZrP) nanosheets are carefully controlled to achieve high enzyme binding affinities, excellent loadings, significant retention of the bound enzyme structure, and high enzymatic activities. In specific cases, catalytic activities and selectivities of the nanobiocatalysts are improved over those of the corresponding pristine enzymes. Maximal enzyme structure retention has been obtained by coating the nanosheets with appropriate proteinaceous materials to soften the enzyme-nanosheet interface. These systematic manipulations are of significant importance to understand the complex behavior of enzymes at inorganic surfaces.

Solid phase extraction, separation and preconcentration of rare elements thorium(IV), uranium(VI), zirconium(IV), cerium(IV) and chromium(III) amid several other foreign ions with eriochrome black T anchored to 3-D networking silica gel.

The present work reports the systematic studies on extraction, separation and preconcentration of Th(IV), U(VI), Zr(IV), Ce(IV) and Cr(III) amid several other foreign ions using EBT anchored {SiO2}n3-D microarray. The effect of various sorption parameters, such as pH, concentration, temperature, sample volume, flow-rate and co-existing foreign ions were investigated. Quantitative sorption was ensured at solution pH: 6.0-6.5 for Th(IV), Ce(IV), Cr(III) and pH: 2.75-3.0 for Zr(IV), U(VI) couple. Analysis on extracted species and extraction sites reveals that [Th4(µ(2)-OH)8(H2O)4](8+), [Ce6(µ(2)-OH)12(H2O)5](12+), [Cr3(µ(2)-OH)4(H2O)](5+), [(UO2)3(µ(2)-OH)5(H2O)3](+) and [Zr4(µ(2)-OH)8(H2O)0.5](8+) for the respective metal ions gets extracted at HOMO of the extractor. HOMO-{metal ion species} was found to be 1:1 complexation. Sorption was endothermic, entropy-gaining, instantaneous and spontaneous in nature. A density functional theory (DFT) calculation has been performed to analyze the 3-D structure and electronic distribution of the synthesized extractor.

Adsorption of methyl orange (MO) by Zr (IV)-immobilized cross-linked chitosan/bentonite composite.

A Zr (IV)-immobilized cross-linked chitosan/bentonite composite was synthesized and characterized by Fourier transform infrared, field-emission scanning electron microscopy, and X-ray diffraction techniques. This composite was utilized for the removal of methyl orange (MO) from aqueous solutions. Effects of the loading amount of Zr (IV), initial pH value of MO solutions, adsorbent dosage, and contact time on MO adsorption were considered. The adsorption isotherm data were well described by the Langmuir model, and the maximum adsorption capacity was 438.6mg/g at 303K and natural pH. The kinetic data were well described by the pseudo-second-order model. The thermodynamic data showed that the adsorption process of MO was feasible, spontaneous, and exothermic in nature.

Synthesis, structural, optical and anti-rheumatic activity of metal complexes derived from (E)-2-amino-N-(1-(2-aminophenyl)ethylidene)benzohydrazide (2-AAB) with Ru(III), Pd(II) and Zr(IV).

Three new metal complexes derived from Pd(II), Ru(III) and Zr(IV) with (E)-2-amino-N-(1-(2-aminophenyl)ethylidene)benzohydrazide (2-AAB) have been synthesized. The isolated complexes were characterized by elemental analyses, FT-IR, UV-Vis, ES-MS, (1)H NMR, XRD, thermal analyses (TGA and DTA) and conductance. The morphology and the particle size were determined by transmittance electron microscope (TEM). The results showed that, the ligand coordinates to Pd(II) in the enol form, while it coordinates to Ru(III) and Zr(IV) in the keto form. A square planar geometry is suggested for Pd(II) complex and octahedral geometries are suggested for Ru(III) and Zr(IV) complexes. The optical band gaps of the isolated complexes were measured and indicated the semi-conductivity nature of the complexes. The anti-inflammatory and analgesic activities of the ligand and its complexes showed that, Ru(III) complex has higher effect than the well known drug "meloxicam".