A facile preparation of donut-like supramolecular tannic acid-Fe(III) composite as biomaterials with magnetic,conductive, and antioxidant properties

Tannic acid (TA) complexes with various metal ions are prepared in buffer solutions by readily adjusting the pH, but there is no normalizing method to produce ferric tannate complexes. In this study, TA-Fe(III) complex was prepared in reverse microemulsion medium by reaction of TA as ligand with Fe(III) in 1:3 ligand:metal ion molar ratio. The complex was characterized by SEM, AFM, FT-IR, elemental analysis, AAS measurement, and Brunauer-Emmett-Teller (BET) method. Furthermore, magnetic susceptibility was tested with the Gouy method, and electronic spectral studies of TA-Fe(III) complex were completed with solid UV–vis measurements. The thermal stability was also studied by TGA analysis. These studies show that the ligand molecules have octahedral arrangement around Fe(III) and the complex is paramagnetic. The bandgap energy of the complex was calculated as 3.42 eV with solid UV–vis analysis. To determine antioxidant activity of the complex, Total Phenol Content (TPC) and Trolox Equivalent Antioxidant Concentration (TEAC) methods were used. The complex has great antioxidant properties with TPC = 45 ± 1 mg L^?1 GAE and TEAC = 296 ± 2 mM trolox g^?1 for dry sample.     

Crystal structure, microstructure and reducibility of LaNixCo1−xO3 and LaFexCo1−xO3 Perovskites (0<x≤0.5)

Nickel and iron substituted LaCoO₃ with rhombohedrally distorted perovskite structure were obtained in the temperature range of 600-900 °C by thermal decomposition of freeze-dried citrates and by the Pechini method. The crystal structure, morphology and defective structure of LaCo_1−xNi_xO₃ and LaCo_1−xFe_xO₃ were characterized by X-ray diffraction and neutron powder diffraction, TEM and SEM analyses and electron paramagnetic resonance spectroscopy. The reducibility was tested by temperature programmed reduction with hydrogen. The products of the partial and complete reduction were determined by ex-situ XRD experiments. The replacement of Co by Ni and Fe led to lattice expansion of the perovskite structure. For perovskites annealed at 900 °C, there was a random Ni, Fe and Co distribution. The morphology of the perovskites does not depend on the Ni and Fe content, nor does it depend on the type of the precursor used. LaCo_1−xNi_xO₃ perovskites (x>0.1) annealed at 900 °C are reduced to Co/Ni transition metal and La₂O₃ via the formation of oxygen deficient Brownmillerite-type compositions. For LaCo_1−xNi_xO₃ annealed at 600 °C, Co/Ni metal, in addition to oxygen-deficient perovskites, was formed as an intermediate product at the initial stage of the reduction. The interaction of LaCo_1−xFe_xO₃ with H₂ occurs by reduction of Co³⁺ to Co²⁺ prior to the Fe³⁺ ions. The reducibility of Fe-substituted perovskites is less sensitive towards the synthesis procedure in comparison with that of Ni substituted perovskites.     

Magnetization and EPR of a series of Cr squarate dimers

A series of Cr(III) dimers were synthesized from a parent compound [Cr₂(μ-oxo)₂(μ_1,2-C₄O₄)₂(H₂O)₄]·2H₂O (I) by ligand substitution. The compounds have been analyzed using variable frequency EPR (9–110 GHz) and magnetic susceptibility as a function of field (0–9 T) and temperature (1.9–300 K) to obtain their electronic g-values, exchange energies, and zero-field parameters. The parent compound exhibits a broad maximum around 34 K characteristic of a dimer with antiferromagnetic coupling that fit the Van Vleck susceptibility model well. It was found that the maxima could be tuned from 34 to 80 K by ligand substitution of the waters. Each compound possesses a characteristic color spanning the range of teal to pink. The g-value of each compound was found to be ∼1.98 using spectral simulation. The DMSO derivative is water soluble and has a high LC₅₀ for PC3 cancer cells, suggesting its use as a magnetic resonance imaging agent. X-ray crystal structure of the DMSO derivative [Cr₂(μ-oxo)₂(μ_1,2-C₄O₄)₂(C₂H₆SO)₄]·2H₂O (II) revealed that the DMSO ligands are equatorial, and the squarate groups bridge the two chromiums. This is in contrast to the previously proposed structure of the parent compound where the water ligands were axial and the equatorial squarate groups did not bridge the chromiums. These compounds are interesting because of their ease of synthesis, and their wide range of magnetic behavior. The compounds are good probes into antiferromagnetic dimer exchange by controlling the ligand field surrounding the superexchange pathway present in the molecule.     

A study of the firing temperature of archeological pottery by X-ray diffraction and electron paramagnetic resonance

A fragment of an archeological funerary urn from Campos dos Goytacazes, Brazil, was studied using electron paramagnetic resonance (EPR) and X-ray diffraction (XRD). The thermal stability of all paramagnetic species was studied with isothermal treatment. In the present study, the iron signal (Fe³⁺) cannot be used as a firing temperature reference for archeological pottery. The intensification of this signal with temperature is a consequence of Fe²⁺ oxidation, but this reaction occurs in a short-lived treatment at high temperature or in an extended treatment at lower temperature. However, the iron signal and three other paramagnetic species indicate that the urn was fired for an extended time (up to three days). The thermal stability of the three paramagnetic species indicates a firing temperature of around 500 °C in the inner layer, between 400 and 500 °C in the middle layer, and between 500 and 800 °C in the outer layer. The presence of kaolinite structures only in the middle portion is consistent with the temperature values estimated. A firing method for the funerary archeological urn is suggested.     

The ESR study of single crystal spinel ZnCr2Se4 diluted with Sb and V

The single crystal of Sb³⁺ and V³⁺ doped zinc chromium selenide spinel ZnCr₂Se₄ were prepared by a chemical transport method and characterized by ESR spectroscopy in order to examine the effect of nonmagnetic antimony and magnetic vanadium on properties of the system. For antimony admixtures the Neel temperature is very similar to that of the parent spinel ZnCr₂Se₄ (22 K). However, upon incorporating vanadium ions, the T_N temperature decreases down to 17.5 K, determined for the maximum vanadium content (x=0.06). The temperature dependence of the ESR linewidth over paramagnetic region is interpreted by an occurrence of spin-phonon interaction. The strong broadening linewidth together with its strong temperature dependence for vanadium doped ZnCr₂Se₄ is explained by the complex paramagnetic relaxation model.     

Analysis of two stacked cylindrical dielectric resonators in a TE₁₀₂ microwave cavity for magnetic resonance spectroscopy

The frequency, field distributions and filling factors of a DR/TE??? probe, consisting of two cylindrical dielectric resonators (DR1 and DR2) in a rectangular TE??? cavity, are simulated and analyzed by finite element methods. The TE(+++) mode formed by the in-phase coupling of the TE??(δ)(DR1), TE??(δ)(DR2) and TE??? basic modes, is the most appropriate mode for X-band EPR experiments. The corresponding simulated B(+++) fields of the TE(+++) mode have significant amplitudes at DR1, DR2 and the cavity's iris resulting in efficient coupling between the DR/TE??? probe and the microwave bridge. At the experimental configuration, B(+++) in the vicinity of DR2 is much larger than that around DR1 indicating that DR1 mainly acts as a frequency tuner. In contrast to a simple microwave shield, the resonant cavity is an essential component of the probe that affects its frequency. The two dielectric resonators are always coupled and this is enhanced by the cavity. When DR1 and DR2 are close to the cavity walls, the TE(+++) frequency and B(+++) distribution are very similar to that of the empty TE??? cavity. When all the experimental details are taken into account, the agreement between the experimental and simulated TE(+++) frequencies is excellent. This confirms that the resonating mode of the spectrometer's DR/TE??? probe is the TE(+++) mode. Additional proof is obtained from B?(x), which is the calculated maximum x component of B(+++). It is predominantly due to DR2 and is approximately 4.4 G. The B?(x) maximum value of the DR/TE??? probe is found to be slightly larger than that for a single resonator in a cavity because DR1 further concentrates the cavity's magnetic field along its x axis. Even though DR1 slightly enhances the performance of the DR/TE??? probe its main benefit is to act as a frequency tuner. A waveguide iris can be used to over-couple the DR/TE??? probe and lower its Q to ≈150. Under these conditions, the probe has a short dead time and a large bandwidth. The DR/TE??? probe's calculated conversion factor is approximately three times that of a regular cavity making it a good candidate for pulsed EPR experiments.     

EPR evidence of antiferromagnetic ordering in single‐layer graphene

We report electron paramagnetic resonance (EPR) evidence of the antiferromagnetic ordering in pristine single‐layer graphene. Temperature dependences of the parameters of EPR spectra obtained for vacuum‐processed samples were studied within the temperature range of 4.2–300 K. Our experiment has confirmed recent theoretical predictions that in single‐layer graphene the carrier‐mediated exchange interaction leads to antiferromagnetic coupling. We note some quantitative discrepancies between the theory and experimental findings and discuss their origins. (© 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Effect of WO3 on EPR, structure and electrical conductivity of vanadyl doped WO3·M2O·B2O3 (M=Li, Na) glasses

Glasses with composition xWO₃·(30−x)M₂O·70B₂O₃ (M=Li, Na; 0≤x≤15) doped with 2 mol% V₂O₅ have been prepared using the melt-quench technique. The electron paramagnetic resonance spectra have been recorded in X-band (ν≈9.14 GHz) at room temperature (RT). The spin Hamiltonian parameters, dipolar hyperfine coupling parameter and Fermi contact interaction parameter have been calculated. It is observed that the resultant resonance spectra contain hyperfine structures (hfs) only due to V⁴⁺ ions, which exist as VO²⁺ ions in octahedral coordination with a tetragonal compression in the present glass system. The tetragonality increases with WO₃:M₂O ratio and also there is an expansion of 3d_xy orbit of unpaired electron in the vanadium ion. The study of IR transmission spectra over a range 400-4000 cm⁻¹ depicts the presence of WO₆ group. The DC conductivity (σ) has been measured in the temperature range 423-623 K and is found to be predominantly ionic.     

Identification of radiation‐induced radical structure in azocalix[4]arene: an EPR study

A macrocyclic azocalix[4]arene (1) based ester derivative was synthesized. The single crystals of azocalix[4]arene were produced by slow evaporation of concentrated ethyl acetate solutions. These single crystals were exposed to ⁶⁰Co gamma rays with a dose rate of 0.980 kGy h^‐1 for 48 and 72 h to produce a stable free radical. Electron paramagnetic resonance (EPR) measurements were performed in three mutually perpendicular planes of the single crystal in the magnetic field, in addition, temperature dependence of the EPR signal was studied between 120 K and 450 K. The spectra were found to be temperature and angular dependent. Analysis based on the spectra recorded showed that a free radical was formed by fission of a C–H bond. This radical is described as ^?C_aHC_bH₃ The averages of the principal values of the hyperfine parameters and g‐factor are: g = 2.0034, A_Ha = 1.28 mT, A_H1=H2 = 1.00 mT, and A_H3 = 0.49 mT. Copyright © 2013 John Wiley & Sons, Ltd.