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1.
Nataliia Yu. Strutynska Marina A. Bondarenko Ivan V. Ogorodnyk Igor V. Zatovsky Nikolay S. Slobodyanik Vyacheslav N. Baumer Anna N. Puzan 《Crystal Research and Technology》2015,50(7):549-555
The interaction in the molten system Rb2O‐P2O5‐TiO2‐NiO was investigated at different molar ratios Rb/P = 0.5‐1.3, fixed Ti/P = 0.15, Ti/Ni = 1.0 at temperature range 1073–953 K. The conditions of formation of complex phosphates RbTi2(PO4)3, Rb2Ni0.5Ti1.5(PO4)3 and RbNiPO4 have been determined. The new phosphate Rb2Ni0.5Ti1.5(PO4)3 (space group P213, a = 9.9386(2) Å) has been obtained and investigated by the single crystal X‐ray diffraction and FTIR‐spectroscopy. It has langbeinite‐like structure, that is built up from mixed (Ni/Ti)O6‐octahedra and РО4‐tetrahedra. Rubidium atoms are located in closed cavities of 3D‐framework. 相似文献
2.
Ivan V. Ogorodnyk Igor V. Zatovsky Vyacheslav N. Baumer 《Journal of solid state chemistry》2006,179(12):3681-3687
The single crystals of caesium magnesium titanium (IV) tri-oxo-tetrakis-diphosphate bis-monophosphate, Cs3.70Mg0.60Ti2.78(TiO)3(P2O7)4(PO4)2, crystallize in sp. gr. P-1 (No. 2) with cell parameters a=6.3245(4), b=9.5470(4), c=15.1892(9) Å, α=72.760(4), β=85.689(5), γ=73.717(4), z=1. The titled compound possesses a three-dimensional tunnel structure built by the corner-sharing of distorted [TiO6] octahedra, [Ti2O11] bioctahedra, [PO4] monophosphate and [P2O7] pyrophosphate groups. The Cs+ cations are located in the tunnels. The partial substitution of Ti positions with Mg atoms is observed. The negative charge of the framework is balanced by Cs cations and Mg atoms leading to pronounced concurrency and orientation disorder in the [P2O7] groups, which coordinate both. 相似文献
3.
Ivan V. Ogorodnyk Igor V. Zatovsky Vyacheslav N. Baumer 《Journal of solid state chemistry》2006,179(11):3461-3466
New complex phosphates of the general formula K2M0.5Ti1.5(PO4)3 (M=Mn, Co) have been obtained from the melting mixture of KPO3, K4P2O7, TiO2 and CoCO3·mCo(OH)2 or Mn(H2PO4)2 by means of a flux technique. The synthesized phosphates have been characterized by the single-crystal X-ray diffraction and the FTIR-spectroscopy. The compounds crystallize in the cubic system with the space group P213 and cell parameters a=9.9030(14) Å for K2Mn0.5Ti1.5(PO4)3 and a=9.8445(12) Å for K2Co0.5Ti1.5(PO4)3. Both phosphates are isostructural with the langbeinite mineral and contain four formula unit K2M0.5Ti1.5(PO4)3 per unit cell. The structure can be described using [M2(PO4)3] framework composed of two [MO6] octahedra interlinked via three [PO4] tetrahedra. The Curie-Weiss-type behavior is observed in the magnetic susceptibility. 相似文献
4.
Ivan V. Ogorodnyk Igor V. Zatovsky Vyacheslav N. Baumer Nikolay S. Slobodyanik Oleg V. Shishkin 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(12):i100-i102
Tetrapotassium cerium(IV) zirconium tetrakis(monophosphate) crystallizes in the tetragonal system (space group I41/amd). A complex disorder in K4CeZr(PO4)4 involves the mixing of Ce and Zr atoms on a single site with m2 symmetry and the splitting of P‐ and O‐atom positions, equivalent to a rotation of the phosphate groups, to yield eight‐ and sixfold coordination environments around Ce and Zr, respectively. The K atoms are located in tunnels running parallel to the a and b axes. 相似文献
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6.
I. V. Zatovsky T. I. Ushchapivska N. S. Slobodyanik I. V. Ogorodnyk 《Russian Journal of Inorganic Chemistry》2006,51(1):35-40
The phase formation of complex phosphates in the Na2O-P2O5-Fe2O3-Nb2O5 flux system was studied in the ranges of sodium-to-phosphorus ratios of 0.7–1.2 and iron-to-niobium ratios of 0.9–2.7. The crystallization region and crystallization conditions for the compounds of composition Na3?2x Fe2-x Nbx(PO4)3 (0.8 ≤ x < 1.2) were found. These compounds can be prepared in two (hexagonal and monoclinic) polymorphs. Single-crystal X-ray diffraction experiments were carried out for hexagonal NaFeNb(PO4)3 (space group $R\bar 3$ c, a = 8.590 Å, c = 22.013 Å). The polymorphism in Na3-2x Fe2-x Nbx(PO4)3 complex phosphates is considered as dependent on the preparation parameters. 相似文献
7.
Slobodyanik NS Terebilenko KV Ogorodnyk IV Zatovsky IV Seredyuk M Baumer VN Gütlich P 《Inorganic chemistry》2012,51(3):1380-1385
The possibility of PO(4)(3-) for MoO(4)(2-) partial substitution in the langbeinite framework has been studied by exploration of the K-Fe(Sc)-Mo(W)-P-O systems using the high-temperature solution method. It was shown that 1/3PO(4)(3-) for MoO(4)(2-) substitution leads to formation of three novel compounds K(2)Fe(MoO(4))(PO(4))(2), K(2)Sc(MoO(4))(PO(4))(2), and K(2)Sc(WO(4))(PO(4))(2) with slightly increased lattice parameters and significant distortion of the anion tetrahedra without structure changes. In contrast, the antiferromagnetic structure is modified by substitution in the low-temperature region. The structural peculiarities are discussed in light of bond-valence sums calculations. 相似文献
8.
K. V. Terebilenko N. S. Slobodyanik I.V. Ogorodnyk V. N. Baumer 《Crystal Research and Technology》2014,49(4):227-231
A number of NASICON‐related MIGe2(PO4)3 (MI – Na, K, Ag) have been prepared using a high‐temperature solution method in the molten system MI‐Ge‐P‐O (MI – Na, K) based on the solubility data for GeO2 at 1123 K for the Na‐P‐O system and 1173 K for the K‐P‐O one. The single crystals of AgGe2(PO4)3 were obtained after crystallization of a melt with Ag/P = 1.4. It crystallizes in the trigonal system, space group R‐3, cell parameters a = 8.06340(1) Å, c = 21.8385(4) Å, Z = 6. The framework is built up from two GeO6 units that are isolated from each other by PO4 tetrahedra to form the main building block of the structure [Ge2(PO4)3]−. Two types of silver cations M1 and M2 are found to have different coordination requirements shown by the bond valence sum calculations. 相似文献
9.
Ivan V. Ogorodnyk Igor V. Zatovsky Nikolay S. Slobodyanik Igor P. Vorona 《Journal of solid state chemistry》2007,180(10):2838-2844
Two new mixed valence manganese-containing orthophosphates with a langbeinite structure have been obtained from the complex fluoride-phosphate melts using the high-temperature flux technique. MIVF4 and K2MIVF6 (MIV—Zr, Hf) were used as fluoride and polyvalent metal precursors. Obtained langbeinites were investigated using a single-crystal X-ray diffraction, FTIR-, UV-VIS- and electron paramagnetic resonance (EPR)-spectroscopy. Both compounds crystallize in a cubic system (sp. gr. P213) with cell parameters a=10.2106(12) and 10.1896(9) Å for K1.96Mn0.57Zr1.43(PO4)3 and K1.93Mn0.53Hf1.47(PO4)3, respectively. The rigid langbeinite-like framework is built up from the isolated [MO6] octahedra and [PO4] tetrahedra interlinked via oxygen vertices. Potassium cations occupy positions in the large closed cavities of the framework. Statistical distribution of manganese and tetravalent metal over two crystallographic positions in octahedral oxygen environment can be observed. The presence of the mixed valence manganese in the reported phosphates was confirmed using UV-VIS and EPR-spectroscopy. 相似文献
10.
I. V. Ogorodnyk I. V. Zatovsky V. N. Baumer N. S. Slobodyanik O. V. Shishkin 《Crystal Research and Technology》2007,42(11):1076-1081
Two potassium lanthanide zirconium orthophosphates with general composition K1.822Nd0.822Zr1.178(PO4)3 (KNdZrP) and K2LuZr(PO4)3 (KLuZrP) were prepared using the flux technique. Original synthetic procedure has been examined for the flux growth of the complex phosphates containing zirconium and lanthanide. Both compounds have been synthesized in the complex melts containing at the same time potassium phosphates and transition metal fluorides. The structures were solved from the single crystal (KNdZrP) and powder (KLuZrP) X‐ray diffraction data. Both compounds are isotypic to langbeinite mineral and crystallize in cubic system (sp. gr. P213) with the cell parameters a = 10.3228(2) and a = 10.29668(5) Å respectively. The rigid framework is built up from the isolated [MO6] octahedra and [PO4] tetrahedra interlinked via vertices. The potassium cations are located in the large closed cavities of the framework. (© 2007 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim) 相似文献