Magnetic Susceptibility Measurements Research Articles

Low-temperature cluster spin glass transition in the single-domain NiCr2O4 nanoparticles

NiCr2O4 nanoparticles with average particle size ∼15 nm, a single-domain size maintains the bulk canted antiferromagnetic ground state, were synthesized by a microwave combustion method. The magnetic behavior was carefully investigated by static and dynamic magnetic susceptibility measurements. In addition to a spin-glass-like behavior below paramagnetic-ferrimagnetic transition at T C, the NiCr2O4 nanoparticles demonstrate a low-temperature cluster spin glass transition below the spin canting transition T S, which manifests itself as a magnetic anomaly peak around ∼12 K (at 100 Oe) in the zero-field cooled magnetization with a relatively stronger field dependence in a ‘de Almeida-Thouless’ line for spin glasses. The AC susceptibility analyses in different approaches demonstrate a larger relative peak temperature variation per frequency decade and a longer characteristic relaxation time in the order of 0.04 and 10−7 s, against 0.01 and 10−9 s for the high-temperature blocking, indicating the slow spin dynamics for the low-temperature cluster glassy phase. A field-temperature magnetic phase diagram is proposed for the single-domain NiCr2O4 nanoparticles.

Reaction of Partially Methylated Polygalacturonic Acid with Iron(III) Chloride and Characterization of a New Mixed Chloride-Polygalacturonate Complex.

We have described a new route for the preparation of partially methylated polygalacturonic acid containing hydrolyzed (acidic) and unhydrolyzed (methyl esterified) carboxylate groups in a ratio of 1:1 (PGA, compound 1), and one of its basic FeIII-salts (compound 2) with a ~1:2 FeIII:GA stoichiometry (GA means galacturonic acid and methylated galacturonic acid units). The partially hydrolyzed pectin was transformed into compound 1 with the use of double ion exchange with a strongly acidic macroreticular sulfonated styrene-divinylbenzene copolymer as a hydrogen ion source. The reaction of compound 1 with FeCl3 resulted in compound 2. Compound 2 has a polymeric nature and contains binuclear FeIII(µ-O)(µ-OH)FeIII core units with two kinds of distorted octahedral iron geometries. The salt-forming acidic and methylated GA units of compound 1 are coordinated to FeIII centers in asymmetric bidentate-chelating and -bridging (via C=O group and glycosidic oxygen) modes, respectively. Two kinds of outer-sphere chloride anions were also detected by XPS in various chemical environments fixed by different sets of hydrogen bonds. We also observed a partial reduction of FeIII into FeII due to the ring-opening of the chain-end GA units of compound 1. This reaction provides a new route to determine the number of chain-ends in compound 2, and with the use of the number of GA units calculated from charge neutrality, the average length of these chains and the average molecular weight were also determined. The average molecular weight of the partially methylated polygalacturonic acid used in the industrial-scale production of commercial anti-anemic iron-polygalacturonate agents was ~50,000 g/mol. Compound 2 was also characterized by IR, Mössbauer, and X-ray photoelectron spectroscopy, and magnetic susceptibility measurements. These results on the structure and average molecular weight of basic iron(III) polygalacturonate provide a tool to design Fe-PGA complexes with tuned iron-releasing properties.

The Superconductivity in Bi-Doped BaFe2As2 Single Crystals.

We have successfully synthesized a series of Bi-doped BaFe2As2 high-quality single crystals for the first time. X-ray diffraction (XRD) patterns show an expansion of lattice parameter c with Bi doping, indicating a negative pressure effect. By investigating the resistivity, a Fermi liquid (FL) to non-Fermi liquid (NFL) crossover is observed from normal state to antiferromagnetic order state, accompanied by three superconducting transitions labeled as SC I, SC II and SC III, which are supposed to be induced by three superconducting realms with various Bi concentrations. Thus, we propose that the NFL behavior is closely related to the presence of superconductivity. The magnetic susceptibility measurements further speculate that the SC I and SC III phases should exhibit filamentary superconductivity while the SC II exhibits a possible bulk superconductivity of TC~7 K.

A Dinuclear Copper(II) Complex Electrochemically Obtained via the Endogenous Hydroxylation of a Carbamate Schiff Base Ligand: Synthesis, Structure and Catalase Activity.

In the present work, we report a neutral dinuclear copper(II) complex, [Cu2(L1)(OH)], derived from a new [N,O] donor Schiff base ligand L1 that was formed after the endogenous hydroxylation of an initial carbamate Schiff base H2L coordinated with copper ions in an electrochemical cell. The copper(II) complex has been fully characterized using different techniques, including X-ray diffraction. Direct current (DC) magnetic susceptibility measurements were also performed at variable temperatures, showing evidence of antiferromagnetic behavior. Its catalase-like activity was also tested, demonstrating that this activity is affected by temperature.

A Gadolinium(III) Complex Based on Pyridoxine Molecule with Single-Ion Magnet and Magnetic Resonance Imaging Properties.

Pyridoxine (pyr) is a versatile molecule that forms part of the family of B vitamins. It is used to treat and prevent vitamin B6 deficiency and certain types of metabolic disorders. Moreover, the pyridoxine molecule has been investigated as a suitable ligand toward metal ions. Nevertheless, the study of the magnetic properties of metal complexes containing lanthanide(III) ions and this biomolecule is unexplored. We have synthesized and characterized a novel pyridoxine-based GdIII complex of formula [GdIII(pyr)2(H2O)4]Cl3 · 2 H2O (1) [pyr = pyridoxine]. 1 crystallizes in the triclinic system and space group Pī. In its crystal packing, cationic [Gd(pyr)2(H2O)4]3+ entities are connected through H-bonding interactions involving non-coordinating water molecules and chloride anions. In addition, Hirshfeld surfaces of 1 were calculated to further investigate their intermolecular interactions in the crystal lattice. Our investigation of the magnetic properties of 1, through ac magnetic susceptibility measurements, reveals the occurrence of a slow relaxation in magnetization in this mononuclear GdIII complex, indicating an unusual single-ion magnet (SIM) behavior for this pseudo-isotropic metal ion at very low temperatures. We also studied the relaxometric properties of 1, as a potential contrast agent for high-field magnetic resonance imaging (MRI), from solutions of 1 prepared in physiological serum (0.0-3.2 mM range) and measured at 3 T on a clinical MRI scanner. The values of relaxivity obtained for 1 are larger than those of some commercial MRI contrast agents based on mononuclear GdIII systems.

Synthesis of Manganese(II), Iron(III), and Vanadium(IV) Complexes with New Schiff Bases and their Spectroscopic and Thermal Studies and Evaluation of their Antimicrobial Activity

Heterocyclic 3-acetyl coumarin with hydrazide derivatives and their metal complexes are a substantial family of pharmaceutical drugs used to treat infection, anti-inflammatory issues, diabetes, and neurological disorders in the field of medicinal chemistry. Cyclization of 5- floro-2-furaldehyde, ethyl acetoacetate, and urea or thiourea by LaCl3.7H2O, addition of hydrazine to form amine derivatives were performed, and respective Schiff base derivatives (L1, L2) were produced by adding acetyl coumarin in an ethanolic solution at ambient temperature. New ligands and its complexes of the V (IV), Fe (III) and Mn (II) ions were characterized using (FT-IR, UV, MS) and nuclear magnetic resonance (1H-NMR) as well as elemental analysis (CHN). The synthesized complexes chelate with ligands L1, L2 via (N, O2) atoms. The structural geometry of the complexes was illustrated in the solid phase using FT-IR and UV-VIS spectroscopy, elemental analysis (CHNS), and flame atomic absorption, in addition to magnetic susceptibility and conductivity measurement. The antibacterial activity of the newly prepared ligands and their metal complexes was evaluated against Pseudonomous aerugionosa as a gram negative and Bacillus subtilis as a gram positive microorganism. Moreover, the antifungal activity against two fungi Aspergillus flavus, and Saccharomyces cerevisiae was studied for all compounds. The coordinated ligands significantly increased their bactericidal and fungicidal action compared to the free ligands, which did not exhibit any activity against the selected fungal and bacterial strains. The results focused on the synergetic relationship between the metal ion and the ligand, in addition to the structural variation.

Complexes of 2-hydroxynaphthylidene-2-aminothiazole with Titanium (III) and Vanadium (III)

The synthesis and characterization of a new series of metal complexes of Titanium (III) and Vanadium (III) as a metal ion and 2-hydroxynaphthylidene-2-aminothiazole as a ligand are studied. The complexes [C14H15N2SO4.TiCl2] and [C14H13N2SO3.VCl2] have been characterized by elemental, infrared, electronic, absorption spectral, and magnetic susceptibility measurements. An octahedral geometry is predicted for Ti(III) and V(III) complexes.

Superconductivity of a new Ru-based alloy Ru3Sb1.75Sn5.25

We report the synthesis and superconductivity of a new Ru-based alloy Ru3Sb1.75Sn5.25. The single crystal and polycrystal samples were synthesized by the Sn-flux method and solid state reaction, respectively. The Ru3Sb1.75Sn5.25 crystals were characterized by powder X-ray diffraction, electrical resistivity, magnetic susceptibility, and specific heat measurements. We find Ru3Sb1.75Sn5.25 crystallize in the Ir3Ge7-type structure and exhibits superconductivity with onset transition temperature Tc = 4.2 K. Density functional theory calculation on Ru3Sb1.75Sn5.25 unveils multiple peaks of density of states around the Fermi level, which may explain the emergence of superconductivity. Our study provides an example compound to explore the fascinating interplay of superconductivity, electronic band structure and paramagnetism in Ru-based superconductors.

New Fe(III), Co(II), Ni(II), Cu(II), and Zn(II) mixed-ligand complexes: stractural, DFT, biological, and molecular docking studies

The primary objective of the current framework was to synthesize novel mononuclear 1:1:1 complexes involving FeLG, CoLG, NiLG, CuLG, and ZnLG, where the ligand (L) is identified as 4-[(4-oxo-4,5-dihydro-1,3-thiazol-2-yl)hydrazono]methylphenyl-4-methylbenzenesulfonate, and glycine (G) serves as the co-ligand. Comprehensive characterization of the investigated complexes was achieved through various analytical techniques, including FTIR, UV-Vis spectroscopy, elemental analysis, mass spectra, magnetic susceptibility measurements, molar conductivity assessments, and thermogravimetric analysis (TGA). The determination of stoichiometry was performed employing the molar ratio technique, revealing the octahedral geometry inherent in the isolated metal complexes. Employing a density functional theory (DFT) approach, the molecular structures of the designated compounds were theoretically elevated, and quantum chemical descriptors were derived to provide a deeper insight into their electronic properties. Furthermore, the inhibitory potential of these compounds against fungal strains and pathogenic bacteria prevalent in the Arab environment was evaluated using the disc diffusion method, emphasizing their role in combating diseases affecting humans, animals, and plants. Notably, the metal complexes exhibited superior antibacterial activity, as evidenced by a higher activity index. Molecular docking investigations were conducted to ascertain the inhibitory effects of the compounds on the 1FJ4 protein, with ZnLG emerging as the compound with the highest binding affinity. These results suggest the promising candidacy of these compounds as antimicrobial agents, particularly in the context of combating bacterial and fungal infections.
 KEY WORDS: Complexes, Antimicrobial, DFT, Schiff base, Molecular docking
 Bull. Chem. Soc. Ethiop. 2024, 38(2), 397-416. 
 DOI: https://dx.doi.org/10.4314/bcse.v38i2.9

Field-induced Bose–Einstein condensation in zigzag spin chain KGaCu(PO4)2

Single crystals of GaKCu(PO4)2 were synthesized using the hydrothermal method, and subsequent measurements of specific heat, magnetic susceptibility, and high-field magnetization were performed. A broad peak is observed in the magnetic susceptibility and specific heat curves, with the maximum values appearing at about 11.5 K and 5.29 K, respectively. The highest maximum peak value of susceptibility is observed when the magnetic field is applied along the c-axis, followed by the a-axis, b-axis, and polycrystalline samples. These indicate that the system exhibits one-dimensional magnetism and the magnetic easy axis is the c axis. The magnetization at 2 K reveals the occurrence of a field-induced Bose–Einstein condensation (BEC) phase within the magnetic field range of approximately 8−12 T. High-field magnetization up to 40 T indicates that the compound reaches magnetization saturation as the field exceeds H s = 12 T. Through systematic measurements, a field-temperature (H−T) phase diagram was constructed, and dome-like phase boundaries were observed. The findings suggest that GaKCu(PO4)2 is a spin gap system and a promising candidate for studying BEC of magnons due to its phase transition boundary occurring at low magnetic fields.

Synthesis, Biological and Medicinal Evaluation of New Boric Acid Ester Derived From Antibiotic Drug with Some of Its Metal Complexes

Synthesis of new ligand, namely [bis(2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl) hydrogen borate] (BIB), utilizing the reaction of metronidazole with boric acid in mole ratio (2:1), as well as the metal complexes with [Ni(II) and Cu(II)], were synthesized. All synthesized compounds were characterized by utilizing spectroscopic techniques such as FTIR, 1H-NMR, thermal analysis (T.G., UV-Vis), and atomic absorption (A.A.S.), as well as micro elemental analysis (C.H.N.), melting point (m.p), magnetic susceptibility, molar conductivity, and chloride content measurements. All complexes were paramagnetic, and the electrolyte and the suggested geometries were tetrahedral for nickel and octahedral for copper. In addition, all the transition metal complexes produced were shown to be antibacterial and antifungal against the bacteria Staphylococcus aureus, Escherichia coli, and the fungus Candida. Also, metronidazole and the ligand were evaluated as anticancer agents against human breast cancer (MCF-7). The results showed that ligand was more active as an anticancer than metronidazole.

Topsoil's magnetic and electrical properties in a volcanic and tropical region.

Environmental monitoring by measuring topsoil's magnetic and electrical properties is one practical, quick, and low-cost approach. This method has been used worldwide as a proxy for the presence of potentially toxic elements. However, additional research must be conducted on diverse soil types, geology, and climates. We determined the magnetic and electrical properties of urban and agricultural topsoils in a volcanic region and analyzed them as possible proxies of potentially toxic elements for environmental monitoring. To identify topsoil characteristics, we employed the measurements of magnetic susceptibility and hysteresis, electrical conductivity, total dissolved solids, power of hydrogen (pH), particle morphology, and element contents that were statistically analyzed to identify relevant properties. The result was able to differentiate volcanic soils from urban, industrial, and agricultural areas as well. The value of low-frequency magnetic susceptibility (χLF) in soils from urban areas is higher than 866.0±249.9 ×10-8 m3 kg-1, while the value of χLF in agricultural areas is 208.0±67.8 ×10-8 m3 kg-1. This is reinforced by the relationship between low-frequency and frequency-dependent magnetic susceptibility (χLF-χFD%) in samples from urban areas that fall within the same cluster dominated by coarse-grained magnetic minerals originating from anthropogenic processes. In contrast, the agricultural area forms a separate cluster primarily influenced by pedogenic processes from acid igneous rock minerals. Caution is required for interpreting the magnetic signal due to the high contents of lithogenic magnetic particles inherited from the parent materials of Andisols.

Modifying the valence phase transition in Eu2Al15Pt6 by the solid solutions Eu2Al15(Pt1−x T x )6 (T = Pd, Ir, Au; x = 1/6)

Abstract The solid solutions Eu2Al15(Pt1−x T x )6 with T = Pd, Ir, Au and x = 1/6 were prepared by arc-melting the stoichiometric mixture of the elements, and subsequent annealing. For x = 1/6, all three solid solutions adopt the same structure type as Eu2Al15Pt6 according to powder X-ray diffraction data. Since the platinide Eu2Al15Pt6 exhibits a (3 + 1)D modulated structure (approximant in space group P121/m1), only the averaged hexagonal unit cell (P63/mmc, Sc0.6Fe2Si4.9 type) was refined by the Rietveld method. Scanning electron microscopy in combination with energy-dispersive X-ray spectroscopy (SEM/EDX) showed that the degree of substitution is in line with the weighed amounts. For values of x > 1/6, no phase-pure samples could be obtained. The results of the magnetic susceptibility measurements indicate that the isoelectronic substitution of Pd for Pt lowers the temperature of the first-order valence phase transition from T trans = 45 K in Eu2Al15Pt6 to T trans = 42 K in Eu2Al15(Pt5/6Pd1/6)6. For Eu2Al15(Pt5/6Ir1/6)6 and Eu2Al15(Pt5/6Au1/6)6 a change in the electronic situation occurs since the Ir substituted compound exhibits one electron less compared to the pristine Pt compound, while Eu2Al15(Pt5/6Au1/6)6 has one additional electron. As a consequence, Eu2Al15(Pt5/6Ir1/6)6 shows a higher valence phase transition temperature of T trans = 52 K while for Eu2Al15(Pt5/6Au1/6)6 no such transition is obvious.

Synthesis, characterisation and antibacterial study of copper(ii) complexes of new benzylacetone-benzoylhydrazone and its <i>para</i>-nitro and <i>para</i>-hydroxy substituted analogues

Three new ligands viz, benzylacetone-enzoylhydrazone [babh (L1)], para-hydroxy-benzylacetone-benzoylhydrazone [p-OH-babh (L2 )] and para-nitrobenzylacetone-benzoylhydrazone [p-NO2 -babh (L3 )], were synthesised by condensation of hydrazides with benzylacetone. The ligands were each reacted with copper(II) salts (chloride, nitrate, acetate and sulphate) to form complexes with the general formulae ML2X2 (X = Cl , NO3 , AcO- and SO4 ). The compounds were characterised using 1H NMR, Infrared and UV-Visible spectroscopy, as 4 well as CHN elemental analyser and magnetic susceptibility measurements. Antibacterial activity of the ligands and synthesised complexes were investigated using the agar diffusion method against two Gram-positive (Staphylococcus aureus NCTC 6571 and Bacillus cereus ATCC 11778) and three Gram- negative (Escherichia coli ATCC 25922, Pseudomonas aeruginosa ATCC 10145, Klebsiella pneumonia ATCC 13048) bacterial strains. However, the observed antimicrobial strength of the synthesized compounds was rather low.

A Novel Approach for Quantifying Magnetic Susceptibility of Aqueous and Organic Solutions.

A new method for measuring the magnetic properties of aqueous and organic solutions is presented. This approach is based on quantifying the force resulting from the sample's interaction with a magnetic field. The experimental setup utilizes neodymium magnets attached to a stepper motor to adjust the distance between the magnets and the test sample, while an analytical balance serves as a strain gauge. Magnetic susceptibility measurements were performed on selected inorganic and organic solutions. A series of finite element simulations allowed us to convert experimental results to physical quantities describing magnetic susceptibilities of substances. The limit of detection (LoD) and limit of quantification (LoQ) values for the developed method of determining magnetic susceptibility were equal to 6.67·10-3 M and 2.02·10-2 M, respectively.

A combined theoretical and experimental approach to determine the right choice of co-ligand to impart spin crossover in Fe(II) complexes based on 1,3,4-oxadiazole ligands.

We present the synthesis of two new novel tetradentate ligands based on 1,3,4-oxadiazole, 2-(2-pyridyl)-5-[N,N-bis(2-pyridylmethyl)aminomethyl]-1,3,4-oxadiazole (LTetraPy-ODA) and 2-(2-phenyl)-5-[N,N-bis(2-pyridylmethyl)aminomethyl]-1,3,4-oxadiazole (LTetraPh-ODA). The ligands were used to prepare six mononuclear complexes [FeII(LTetraPy-ODA)(NCE)] (C1-C3) and [FeII(LTetraPh-ODA)(NCE)] (C4-C6) where E = S, Se or BH3. In addition, the ligand LTetraPy-ODA was employed in the synthesis of a new di-nuclear complex [FeII2(LTetraPh)](ClO4)4·1 CH3NO2·1.5 H2O (C7). Characterization of all complexes was carried out using single-crystal X-ray crystallography, elemental analysis, and infrared spectroscopy. Magnetic susceptibility measurements, performed in the temperature range of 2-300 K using a SQUID magnetometer, revealed spin crossover behaviour exclusively in the mononuclear complexes C3 and C6, in which two monodentate NCBH3- co-ligands coordinate. The presence of the lattice solvent was found to be crucial to the spin transition property, with complex C3 exhibiting a switching temperature (T1/2) of approximately 165 K and C6 approximately 194 K. The other four mononuclear complexes C1, C2, C4, C5, as well as the dinuclear complex C7 are locked in the high spin state over the measured temperature range. Density Functional Theory (DFT) calculations were performed on complexes C1-C6 to rationalise the observed magnetic behaviour, demonstrating the significant effect of the NCS-, NCSe- and NCBH3- co-ligands ligands on the spin-crossover behaviour of the [FeII(L)(NCE)] complexes.

Photoluminescent and Magnetic Properties of Mononuclear Lanthanide-Based Compounds Containing the Zwitterionic Form of 4-Picolinic Acid as a Ligand

A series of mononuclear lanthanide-based coordination compounds was obtained under mild synthetic conditions and fully characterized. Single-crystal X-ray diffraction reveals six isomorphic compounds of type [Ln(NO3)(4picH)2(H2O)4](NO3)2 (Ln3+ = Sm (1), Eu (2), Gd (3), Tb (4), Dy (5), Er (6)), in which 4picH is the zwitterionic form of the 4-picolinic acid. Except for compounds 3 and 6, a study into the emissive properties of the compounds was carried out, revealing a ligand-sensitized lanthanide-characteristic luminescence. Compounds 2 and 4 are candidates for luminescent probes in solution. At the same time, the chromaticity data for 5 revealed a potential white-light emitter with a correlated color temperature (CCT) value of 6570 K. Alternating current (AC) magnetic susceptibility measurements, supported by theoretical calculations, showed a field-induced slow relaxation of the magnetization and a single-ion magnet behavior for compound 5.

Antibacterial, antibiofilm, and antioxidant activities of two novel metal-organic frameworks (MOFs) based on 4,6-diamino-2-pyrimidinethiol with Zn and Co metal ions as coordination polymers.

In the present era, the increase in free radical species (FRs) and multidrug-resistant (MDR) bacteria represents a major worldwide concern for public health. Biofilm development and the overuse and misuse of antibiotics could lead to the adaptation of bacteria to antimicrobial agents. Consequently, finding novel multifunctional species with antibacterial, antioxidant, and antibiofilm properties has become crucial in the fight against challenging bacterial infections and chronic inflammatory conditions. Metal-organic frameworks (MOFs) with zinc and cobalt metal centers are widely utilized in biological and environmental remediation owing to their versatility. In this study, multifunctional Zn-MOFs and Co-MOFs were successfully synthesized with zinc and cobalt as metal centers and 4,6-diamino-2-pyrimidinethiol as an organic linker using a hydrothermal technique. Numerous characterization techniques were used to fully examine the MOF structure, functionality, chemical makeup, crystalline structure, surface appearance, thermal behavior, and magnetic characteristics; the techniques included XPS, PXRD, FTIR, FESEM, EDX, UV-visible, BET, BJH, TGA/DTG, DSC, and magnetic susceptibility measurement. The antioxidant, antibacterial, and antibiofilm activities of the MOFs were examined, and they demonstrated potent activity in each of these aspects. The proposed mechanisms of antibacterial activity suggest that bacterial cell death results from multiple toxic effects, including electrostatic interaction and lipid peroxidation, when MOFs are attached to bacteria, leading to the formation of reactive oxygen species (ROSs). Zn-MOFs exhibit high antibacterial and antibiofilm efficacy owing to their large surface-to-volume ratio and porous nature, while Co-MOFs exhibit high antioxidant capacity owing to their redox properties.

Questing for homoleptic mononuclear manganese complexes with monodentate O-donor ligands.

Compounds containing Mn-O bonds are of utmost importance in biological systems and catalytic processes. Nevertheless, mononuclear manganese complexes containing all O-donor ligands are still rare. Taking advantage of the low tendency of the pentafluoroorthotellurate ligand (teflate, OTeF5) to bridge metal centers, we have synthesized two homoleptic manganese complexes with monomeric structures and an all O-donor coordination sphere. The tetrahedrally distorted MnII anion, [Mn(OTeF5)4]2-, can be described as a high spin d5 complex (S = 5/2), as found experimentally (magnetic susceptibility measurements and EPR spectroscopy) and using theoretical calculations (DFT and CASSCF/NEVPT2). The high spin d4 electronic configuration (S = 2) of the MnIII anion, [Mn(OTeF5)5]2-, was also determined experimentally and theoretically, and a square pyramidal geometry was found to be the most stable one for this complex. Finally, the bonding situation in both complexes was investigated by means of the Interacting Quantum Atoms (IQA) methodology and compared to that of hypothetical mononuclear fluoromanganates. Within each pair of [MnXn]2- (n = 4, 5) species (X = OTeF5, F), the Mn-X interaction is found to be comparable, therefore proving that the similar electronic properties of the teflate and the fluoride are also responsible for the stabilization of these unique species.

Synthesis of New Mn(II), Co(II) and Cu(II) Complexes Grabbed in Novel Functionalized Ionic Liquid Tagged Schiff base: Physico-chemical Properties and Antibacterial Applications

An ionic liquid tagged schiff base, [1-{2-(2-hydroxybenzylideneamino)ethyl}-3-methylimidazolium]PF6 was synthesized from a functionalized ionic liquid (FIL) 2-aminoethyl-3-methylimidazolium hexafluorophosphate, [2-aemim]PF6 and salicylaldehyde without using any organic solvent. The Schiff base was used as a ligand to trap Mn(II), Co(II), Cu(II) ions from its corresponding metal acetates and to form the new transition metal complexes. The synthesized Mn(II), Co(II), Cu(II) complexes along with the Schiff base were characterized by ESI-MS, PXRD, UV-Visible, FT-IR, 1H NMR spectroscopic and analytical (elemental analysis and magnetic susceptibility measurements) methods. Based on these spectral analysis data tetra coordinated geometries were assigned for the newly synthesized metal(II) complexes. Antibacterial sensitivity of the Schiff base and the Mn(II), Co(II), Cu(II) complexes were evaluated against gram positive (Staphylococcus aureus) and gram negative (Escherichia coli) bacteria to assess their minimum zone of inhibition.