G. Leniec

Growth, optical and EPR properties of Li1.72Na0.28Ge4O9 single crystals pure and slightly doped with Cr

Single crystals of lithium-sodium-tetragermanate, a member of the solid solution series Li2−xNaxGe4O9 with x=0.28, pure and slightly doped with Cr3+ ions (0.03 mol.% and 0.1 mol.%), were grown in ambient atmosphere by the Czochralski technique from stoichiometric melt. The crystals with dimensions up to 20 mm in diameter and 50 mm in length were obtained. The crystal structure has been determined by means of X-ray diffraction. Phase analysis and structural refinement of the Li1.72Na0.28Ge4O9 crystals were performed by X-ray powder diffraction using Ni-filtered Cu Kα radiation with a Siemens D5000 diffractometer. The absorption, excitation and photoluminescence spectra of the crystals were measured in the UV-VIS and IR range at low temperatures. EPR investigations were performed using a conventional X-band Bruker ELEXSYS E 500 CW-spectrometer operating at 9.5 GHz with 100 kHz magnetic field modulation. Temperature and angular dependences of the EPR spectra of the crystal samples were recorded in the 3–300 K temperature range.

EPR and optical properties of KYb(WO4)2 and KTb0.2Yb0.8(WO4)2 single crystals

Well oriented KYb(WO4)2 and KTb0.2Yb0.8(WO4)2 single crystals have been investigated for their magnetic and optical properties using the Raman and EPR techniques. The registered EPR signal is dominated by three lines ascribed to ytterbium ions: one main and two satellites. Tb ions, although non-paramagnetic, distinctly modify magnetic properties of the KYb(WO4)2 single crystal. Basic parameters of the spin Hamiltonian, including Zeeman and hyperfine terms (g and A matrices) as well the spatial orientation between principal and crystallographic axes systems were determined for both crystals.

Growth and EPR properties of KSm(WO4)2 and KEr(WO4)2 single crystals

Growth conditions and electron paramagnetic resonance investigations of two well oriented KSm(WO4)2 and KEr(WO4)2 single crystals have been presented and discussed. Hyperfine structure of Sm3+ ion was detected and analyzed for angular and temperature dependences. EPR spectra of KEr(WO4)2 and its angular dependence showed the presence of 5 magnetically nonequivalent Er centers in the crystal. A change in the type of magnetic interactions was analyzed using mixed (Gaussian and Lorentzian) fits of the EPR spectra.

Growth and EPR properties of ErVO4 single crystals

Abstract Single crystals of ErVO4 were grown by the Czochralski method under ambient pressure in a nitrogen atmosphere. Obtained crystals were transparent with strong pink coloring. Electron paramagnetic resonance (EPR) spectra were recorded as a function of the applied magnetic field. Temperature and angular dependences of the EPR spectra of the samples in the 3–300 K temperature range were analyzed applying both Lorentzian––Gauss approximation for diluted medium and Dyson for dense magnetic medium. EPR-NMR program was done to find local symmetry and spin Hamiltonian parameters of erbium ions.

Spectroscopic properties and molecular structure of copper phytate complexes: IR, Raman, UV–Vis, EPR studies and DFT calculations

The copper phytate IP6Cu, IP6Cu2 and IP6Cu3 complexes were synthesized changing the phytate to metal mole ratio. The obtained products have been characterized by means of chemical and spectroscopic studies. Spectroscopic ATR/IR, FT-Raman, UV–Vis, EPR and magnetic measurements were carried out. The structures of these compounds have been proposed on the basis of the group theory and geometry optimization taking into account the shape and number of the bands corresponding to the stretching and bending vibrations of the phosphate group and metal–oxygen polyhedron. The role of the inter- and intra-hydrogen bonds in stabilization of the structure has been discussed. EPR studies showed that a local rhombic symmetry of copper ions appears in the studied phytates. Dominant interactions show antiferromagnetic properties depending on the content of paramagnetic ions.

Spectroscopic and Magnetic Properties of Gadolinium Macroacyclic and Macrobicyclic Complexes

As a result of the Schiff base condensation the gadolinium macroacyclic and macrobicyclic Schiff base complexes have been synthesized and investigated by infrared spectroscopy (IR) and electron paramagnetic resonance (EPR). Both electron ionization and electron spray Molecular Spectroscopy spectra confirmed the [1:1] proportion of a ligand to metal in gadolinium macrocyclic and mocrobicyclic Schiff base complex samples. The thermogravimetrydifferential thermal analysis (TG-DTA) indicated the presence of two water molecules in the innersphere of the macrobicyclic complex and confirmed no water coordination of the metal ion in the macroacyclic complex. The temperature dependence of the integrated intensity of the EPR spectra enabled the magnetic interactions in the spin system of these compounds to be revealed.