scholarly journals Na7Mg13Nd(PO4)12

2012 ◽  
Vol 68 (6) ◽  
pp. i44-i44 ◽  
Author(s):  
Hasna Jerbi ◽  
Mourad Hidouri ◽  
Ben Amara Mongi
Keyword(s):  
Crystal Structure ◽  
Ternary System ◽  
Three Dimensional ◽  
Mirror Plane ◽  
Site Symmetry ◽  
Flux Method ◽  
Structural Units ◽  
Quasi Ternary System

Investigations of the quasi-ternary system Na3PO4–Mg3(PO4)2–NdPO4 allowed us to obtain the new phosphate heptasodium tridecamagnesium neodymium dodecakisphosphate, Na7Mg13Nd(PO4)12, by applying a flux method. The crystal structure is isotypic with that of the previously reported Na7Mg13 Ln(PO4)12 (Ln = Eu, La) compounds. It consists of a complex three-dimensional framework built up from an NdO8 polyhedron (m symmetry), an MO6 octahedron statistically occupied by M = Mg and Na, and eight MgO x (x = 5, 6) polyhedra (four with site symmetry m), linked either directely by sharing corners, edges and faces, or by one of the eight unique PO4 tetrahedra through common corners. Two of the PO4 tetrahedra are statisticaly disordered over a mirror plane. The whole structure can be described as resutling from an assembly of two types of structural units, viz [Mg4 MP4O22]∞ 2 layers extending parallel to (100) and stacked along [100], and [Mg4NdP4O36]∞ 1 undulating chains running along the [010] direction. The six different Na+ cations (five with site symmetry m and one with 0.5 occupancy) are situated in six distinct cavities delimited by the framework. The structure was refined from data of a racemic twin.

scholarly journals Ionothermal synthesis and crystal structure of a new organic–inorganic hybrid compound:catena-poly[bis(1-ethyl-3-methylimidazolium) [hepta-μ-bromido-pentacuprate(I)]]

2014 ◽  
Vol 70 (11) ◽  
pp. 1021-1024
Author(s):  
Ljiljana Karanović ◽  
Dejan Poleti ◽  
Tamara Đorđević
Keyword(s):  
Crystal Structure ◽  
Three Dimensional ◽  
Mirror Plane ◽  
Site Symmetry ◽  
Small Contribution ◽  
Hybrid Compound ◽  
Coordination Environment ◽  
Synthesis And Crystal Structure ◽  
Inorganic Hybrid ◽  
Dimensional Network

A new organic–inorganic hybrid compound,catena-poly[bis(1-ethyl-3-methylimidazolium) [μ5-bromido-tri-μ3-bromido-tri-μ2-bromido-pentacuprate(I)]], {(C6H11N2)2[Cu5Br7]}n, has been obtained under ionothermal conditions from a reaction mixture containing Ba(OH)2·8H2O, Cu(OH)2·2H2O, As2O5, 1-ethyl-3-methylimidazolium bromide and distilled water. The crystal structure consists of complex [Cu5Br7]2−anions arranged in sinusoidal {[Cu5Br7]2−}nchains running along theaaxis, which are surrounded by 1-ethyl-3-methylimidazolium cations. Three of the five unique Br atoms and one of the three CuIatoms occupy special positions with half-occupancy (a mirror plane perpendicular to thebaxis, site symmetrym). The CuIions are in a distorted tetrahedral coordination environment, with four Br atoms at distances ranging from 2.3667 (10) to 2.6197 (13) Å, and an outlier at 3.0283 (12) Å, exceptionally elongated and with a small contribution to the bond-valence sum of only 6.7%. Short C—H...Br contacts build up a three-dimensional network. The Cu...Cu distances within the chain range from 2.8390 (12) to 3.0805 (17) Å, indicating the existence of weak CuI...CuIcuprophilic interactions.

catena-Poly[[aqua(N,N-dimethylformamide-κO)strontium(II)]-bis[μ-2-(4-carboxyphenoxy)propionato-κ3 O,O′:O′]]

2007 ◽  
Vol 63 (11) ◽  
pp. m2849-m2849 ◽  
Author(s):  
Li-Li Kong ◽  
Shan Gao ◽  
Li-Hua Huo ◽  
Seik Weng Ng
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonding ◽  
Water Molecule ◽  
Three Dimensional ◽  
Mirror Plane ◽  
Zigzag Chain ◽  
Site Symmetry ◽  
Acceptor Site ◽  
Special Position ◽  
Dimensional Network

In the crystal structure of the polymeric title compound, [Sr(C10H9O5)2(C3H7NO)(H2O)] n , the SrII atom is O,O′-chelated by the carboxylate end of two 2-(4-carboxyphenoxy)propionate monoanions, and is coordinated by a water molecule and a dimethylformamide (DMF) molecule. It also interacts with the carboxylate O atom of two adjacent monoanions; these bonds give rise to a zigzag chain along the a axis. Meanwhile, the carboxyl –CO2H end of the anion interacts with an acceptor site [O...O = 2.629 (4) Å]; this interaction and hydrogen bonding involving the water molecule [O...O = 3.191 (5) Å] give rise to a three-dimensional network. The eight coordinating O atoms comprise an irregular polyhedron around the metal atom. The Sr atom, the water O atom, and the N and O atoms of the DMF molecule lie on a special position of site symmetry m; the DMF molecule is disordered about the mirror plane.

A New Strontium Lithium Titanium Oxide, SrLi2Ti6O14: Crystal Growth and Structure Determination

2002 ◽  
Vol 57 (5) ◽  
pp. 512-518 ◽  
Author(s):  
I. Koseva ◽  
P. Peshev ◽  
S. Pechev ◽  
P. Gravereau ◽  
J.-P. Chaminade
Keyword(s):  
Crystal Structure ◽  
Crystal Growth ◽  
Ternary System ◽  
Lithium Titanate ◽  
Mirror Plane ◽  
Tetrahedral Coordination ◽  
Flux Method ◽  
Orthorhombic Space Group ◽  
X Ray ◽  
Lithium Titanium

A new strontium lithium titanate with composition SrLi2Ti6O14 has been discovered in the ternary system SrO - Li2O - TiO2. Single crystals of this compound have been grown by the flux method. The structure of SrLi2Ti6O14 has been solved using X-ray data (Mo-Kα radiation, orthorhombic, space group Cmca, Z = 8, with a = 16.570(5), b = 11.150(2), c = 11.458(2) Å , R1 = 0.039 (wR2 = 0.087)). The crystal structure is built by edge and corner sharing TiO6 octahedra which form layers parallel to the (100) plane. Consecutive layers [deduced from a mirror plane parallel to (100)] are linked by common corners in the a direction. Lithium atoms in tetrahedral coordination occupy vacancies of the framework of titanium octahedra, while strontium atoms lie in 11-coordinated sites between two successive layers.

scholarly journals Dilithium disodium nickel(II) cyclohexaphosphate dodecahydrate, Li2Na2NiP6O18·12H2O

2012 ◽  
Vol 68 (8) ◽  
pp. i62-i63 ◽  
Author(s):  
Sonia Abid ◽  
Salem S. Al-Deyab ◽  
Mohamed Rzaigui
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonds ◽  
Three Dimensional ◽  
Chair Conformation ◽  
Internal Symmetry ◽  
Site Symmetry ◽  
Special Position ◽  
Tetrahedral Environment ◽  
Anionic Charge

The crystal structure of Li2Na2NiP6O18·12H2O is characterized by the presence of six-membered P6O186−phosphate ring anions (internal symmetry -1) having a chair conformation and three different cations,viz.Li+, Na+and Ni2+, to counterbalance the anionic charge. All atoms are in general positions except for nickel, which lies on a special position with site symmetry 2. Lithium has a tetrahedral environment (LiO4), and sodium and nickel have octahedral environments [NaO6and Ni(H2O)6, respectively]. The P6O18rings are linkedviacorner sharing by NaO6octahedra and LiO4tetrahedra to form a three-dimensional framework presenting tunnels running along [010] in which the six-coordinated Ni2+cations are located. The structure is stabilized by a network of O—H...O hydrogen bonds.

scholarly journals Crystal structure of 1-methyl-4-methylsulfanyl-1H-pyrazolo[3,4-d]pyrimidine

2014 ◽  
Vol 70 (12) ◽  
pp. o1281-o1281 ◽  
Author(s):  
Mohammed El Fal ◽  
Youssef Ramli ◽  
El Mokhtar Essassi ◽  
Mohamed Saadi ◽  
Lahcen El Ammari
Keyword(s):  
Crystal Structure ◽  
Title Compound ◽  
Three Dimensional ◽  
Pyrimidine Ring ◽  
Ring System ◽  
Dimensional Structure ◽  
Mirror Plane ◽  
Three Dimensional Structure ◽  
Π Interactions ◽  
Compound C

In the title compound, C7H8N4S, the non-H atoms of the pyrazolo[3,4-d]pyrimidine ring system and the methylsulfanyl group lie on a crystallographic mirror plane. In the crystal, molecules are linkedviaa number of π–π interactions [centroid–centroid distances vary from 3.452 (7) to 3.6062 (8) Å], forming a three-dimensional structure.

scholarly journals Crystal structure offac-trichlorido[tris(pyridin-2-yl-N)amine]chromium(III)

2015 ◽  
Vol 71 (1) ◽  
pp. 73-75 ◽  
Author(s):  
Yukiko Yamaguchi-Terasaki ◽  
Takashi Fujihara ◽  
Akira Nagasawa ◽  
Sumio Kaizaki
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonding ◽  
Complex Molecule ◽  
Three Dimensional ◽  
Mirror Plane ◽  
Neutral Complex ◽  
Distorted Octahedral Coordination ◽  
Hydrogen Bonding Interactions ◽  
Dimensional Network ◽  
Distorted Octahedral

In the neutral complex molecule of the title compound,fac-[CrCl3(tpa)] [tpa is tris(pyridin-2-yl)amine; C15H12N4], the CrIIIion is bonded to three N atoms that are constrained to afacialarrangement by the tpa ligand and by three chloride ligands, leading to a distorted octahedral coordination sphere. The average Cr—N and Cr—Cl bond lengths are 2.086 (5) and 2.296 (4) Å, respectively. The complex molecule is located on a mirror plane. In the crystal, a combination of C—H...N and C—H...Cl hydrogen-bonding interactions connect the molecules into a three-dimensional network.

scholarly journals Crystal structure of langbeinite-related Rb0.743K0.845Co0.293Ti1.707(PO4)3

2015 ◽  
Vol 71 (3) ◽  
pp. 251-253 ◽  
Author(s):  
Nataliia Yu. Strutynska ◽  
Marina A. Bondarenko ◽  
Ivan V. Ogorodnyk ◽  
Vyacheslav N. Baumer ◽  
Nikolay S. Slobodyanik
Keyword(s):  
Crystal Structure ◽  
High Temperature ◽  
Point Group ◽  
Three Dimensional ◽  
Type Structure ◽  
Group Symmetry ◽  
Site Symmetry ◽  
Point Group Symmetry ◽  
Crystallization Method ◽  
Temperature Crystallization

Potassium rubidium cobalt(II)/titanium(IV) tris(orthophosphate), Rb0.743K0.845Co0.293Ti1.707(PO4)3, has been obtained using a high-temperature crystallization method. The obtained compound has a langbeinite-type structure. The three-dimensional framework is built up from mixed-occupied (Co/TiIV)O6octahedra (point group symmetry .3.) and PO4tetrahedra. The K+and Rb+cations are statistically distributed over two distinct sites (both with site symmetry .3.) in the large cavities of the framework. They are surrounded by 12 O atoms.

The Quasi-Ternary System Ag2S—CdS—GeS2 and the Crystal Structure of Ag2CdGeS4.

ChemInform ◽  
2005 ◽  
Vol 36 (39) ◽  
Author(s):  
O. V. Parasyuk ◽  
L. V. Piskach ◽  
I. D. Olekseyuk ◽  
V. I. Pekhnyo
Keyword(s):  
Crystal Structure ◽  
Ternary System ◽  
Quasi Ternary System

scholarly journals Synthesis, crystal structure and charge-distribution validation of a new alluaudite-type phosphate, Na2.22Mn0.87In1.68(PO4)3

2020 ◽  
Vol 76 (8) ◽  
pp. 1369-1372
Author(s):  
Abdessalem Badri ◽  
Inmaculada Alvarez-Serrano ◽  
María Luisa López ◽  
Mongi Ben Amara
Keyword(s):  
Crystal Structure ◽  
Single Crystals ◽  
Three Dimensional ◽  
Structure Type ◽  
X Ray Diffraction ◽  
Flux Method ◽  
X Ray ◽  
Coordination Numbers ◽  
Dimensional Network ◽  
Anionic Framework

Na2.22Mn0.87In1.68(PO4)3, sodium manganese indium tris(phosphate) (2.22/0.87/1.68), was obtained in the form of single crystals by a flux method and was structurally characterized by single-crystal X-ray diffraction. The compound belongs to the alluaudite structure type (space group C2/c) with general formula X(2)X(1)M(1)M(2)2(PO4)3. The X(2) and X(1) sites are partially occupied by sodium [occupancy 0.7676 (17) and 1/2] while the M(1) and M(2) sites are fully occupied within a mixed distribution of sodium/manganese(II) and manganese(II)/indium, respectively. The three-dimensional anionic framework is built up on the basis of M(2)2O10 dimers that share opposite edges with M(1)O6 octahedra, thus forming infinite chains extending parallel to [10\overline{1}]. The linkage between these chains is ensured by PO4 tetrahedra through common vertices. The three-dimensional network thus constructed delimits two types of hexagonal channels, resulting from the catenation of M(2)2O10 dimers, M(1)O6 octahedra and PO4 tetrahedra through edge- and corner-sharing. The channels are occupied by Na+ cations with coordination numbers of seven and eight.

scholarly journals Benzene-1,2-diaminium bis(hydrogen phosphonate)

IUCrData ◽  
2016 ◽  
Vol 1 (10) ◽  
Author(s):  
Md. Zahid ◽  
R. Akilan ◽  
T. Ganesh ◽  
R. Mohan Kumar ◽  
G. Chakkaravarthi
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonds ◽  
Three Dimensional ◽  
Mirror Plane ◽  
Asymmetric Unit ◽  
Π Interactions ◽  
Centroid Distance ◽  
Molecular Salt ◽  
Ring Motif

The asymmetric unit of the title molecular salt, C6H10N2 2+·2H2PO3 −, contains half of a benzene-1,2-diaminium cation and a phosphite anion, the complete cation being generated by a crystallographic mirror plane. In the crystal, N—H...O hydrogen bonds generate R 2 2(9) and R 2 2(8) ring motifs and O—H...O hydrogen bonds generate an R 2 2(8) ring motif. Overall, these generate a three-dimensional framework. The crystal structure also features π–π interactions [centroid-to-centroid distance = 3.8642 (7) Å].

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