Synthesis and spectroscopic characterization of Cu(II) containing chlorocadmiumphosphate Cd(HPO4)Cl·[H3N(CH2)6NH3]0.5 crystals.

Chlorocadmiumphosphate Cd(HPO(4))Cl·[H(3)N(CH(2))(6)NH(3)](0.5) crystals containing Cu(II) ions have been successfully synthesized at room temperature by using organic amine 1,6-diamino hexane as a template. The samples are characterized by X-ray powder diffraction, Thermal and spectroscopic studies. These are crystallizes in the monoclinic crystal system with cell dimensions: a=1.7697, b=0.6576, c=1.9026nm and ß=106.5°. FT-IR spectrum showed the absorption bands related to PO(4), NH(3)(+) ions and other organic molecule vibrations originated from the templated molecule. The prepared crystals are stable at room temperature and as well as up to around 300°C which were confirmed by thermal analysis. Optical absorption and EPR studies suggest that Cu(II) ion enters in to the lattice as tetragonally distorted octahedral symmetry, for which crystal field and spin-Hamiltonian parameters are calculated. Bonding parameters are suggesting that there exists partial covalent nature between Cu(II) ions and ligands.

Optical and EPR studies of iron bearing phosphate minerals: satterlyite and gormanite from Yukon Territory, Canada.

The iron phosphate minerals satterlyite and gormanite have been investigated by EPR and optical absorption studies. The optical results indicate the presence of ferrous and ferric ions in both minerals. In gormanite the site symmetry of Fe(III) is near octahedral whereas in satterlyite it is tetragonally distorted. On the other hand, the Fe(II) ions are in tetragonally distorted octahedral site in both minerals. In satterlyite the EPR results indicate the presence of the ferric ion in a tetragonally distorted state together with a small percentage of Mn(II). Crystal field (Dq) and interelectronic parameters (B and C) are evaluated.

Single crystal EPR and optical studies of paramagnetic ions doped zinc potassium phosphate hexahydrate--part I: Cu(II)--a case of orthorhombic symmetry.

Single crystal electron paramagnetic resonance (EPR) studies on Cu(II) doped zinc potassium phosphate hexahydrate (ZPPH) were carried out at room temperature. The angular variation spectra in the three orthogonal planes indicate that the paramagnetic impurity has entered the lattice substitutionally in place of Zn(II) and the spin Hamiltonian parameters calculated from these spectra are g(xx) = 2.188, g(yy) = 2.032, g(zz) = 2.373, Axx = 50 G, Ayy = 65.0 G and Azz = 80 G. The g and A tensors were coincident and these values matched fairly well with the values obtained from powder spectrum. The bonding parameters have also been calculated.

Single crystal EPR and optical studies of paramagnetic ions doped zinc potassium phosphate hexahydrate--part II: VO(II)--a case of substitutional site.

Single crystal electron paramagnetic resonance (EPR) studies were carried at room temperature for VO(II) doped zinc potassium phosphate hexahydrate. The results indicate that the paramagnetic impurity has entered the lattice only substitutionally, as confirmed by the single crystal rotations. The spin Hamiltonian parameters calculated from the spectra are g parallel = 1.9356, g perpendicular = 1.9764, A parallel = 200.9 G and A perpendicular = 76.5 G. The optical absorption spectrum exhibits three bands (800, 670 and 340 nm) suggesting the C4v symmetry and the optical parameters evaluated are Dq = 1492, Ds = -3854 and Dt = 186 cm(-1).