Dimere und polymere Pnictidostannat(IV)-Anionen -Darstellung und Kristallstrukturen von Na2K3[SnP3], Na2Cs3[SnP3] und Na2K3[SnBi3] / Dimeric and Polymeric Pnictidostannate(IV) Anions -Preparation and Crystal Structures of Na2K3[SnP3], Na2Cs3[SnP3] and Na2K3[SnBi3]

1998 ◽  
Vol 53 (4) ◽  
pp. 405-410 ◽  
Author(s):  
Matthias Asbrand ◽  
Brigitte Eisenmann ◽  
Holger Engelhardt ◽  
Ute Rößler
Keyword(s):  
Crystal Structures ◽  
Covalent Bonding ◽  
Partial Structure ◽  
Alkali Cations ◽  
Orthorhombic System ◽  
Space Group ◽  
Lattice Constants ◽  
Tetrahedral Voids ◽  
Sodium And Potassium

Abstract The metallic lustrous compounds Na2K3[SnP3], Na2Cs3[SnP3], and Na2K3[SnBi3] were prepared from melts of mixtures of the elements. The isotypic compounds Na2K3[SnP3] and Na2Cs3[SnP3] crystallize in the orthorhombic system, space group Cmca (No 64), Z = 8, with lattice constants a = 1996.1 (4)/2047.9(4) pm, b = 669.5(1)/686.5(2) pm, c = 1494.5(2)/1617.8(3) pm. The structure is characterized by dimeric units [Sn2P6] 10- of edge-sharing [SnP4] tetrahe­dra, which are coordinated by the alkali cations. Na2K3[SnBi3] crystallizes in the orthorhombic system, space group Ibca (No 73), Z = 8, with lattice constants a = 718.2(1) pm , b -1692.6(2) pm, c = 2159.5(2) pm. In the anionic partial structure [SnBi4] tetrahedra are connected via common corners to infinite 1∞[SnBi3]5- Zweier single chains. The sodium and potassium cat­ ions separate the chains from each other. Neglecting the distortions caused by covalent bonding and different radii both structure types can be classified as superstructure defect variants of the Li3Bi structure. Different orderings in the occupation of the tetrahedral voids lead to the variants in the anionic assemblies.

scholarly journals Kristallstruktur und Schwingungsspektrum des Thallium(I)-Zinn(II)-ortho-Thiophosphates TlSnPS4

1987 ◽  
Vol 42 (11) ◽  
pp. 1309-1312 ◽  
Author(s):  
Robert Becker ◽  
Wolfgang Brockner ◽  
Brigitte Eisenmann
Keyword(s):  
Raman Spectrum ◽  
Melting Point ◽  
Title Compound ◽  
Far Infrared ◽  
Orthorhombic System ◽  
Space Group ◽  
Lattice Constants ◽  
Moisture Sensitive

TlSnPS4 crystallizes in the orthorhombic system, space group Pna21 (Nr. 33), Z = 4 with the lattice constants a = 1175.8 (5) pm, b = 890.1 (4) pm, c = 663.3 (4) pm. In the structure are sligthly distorted discrete PS3-4 anions.The far infrared, infrared and Raman spectrum is assigned on the basis of PS3-4 -units with C3v symmetry. According to the DTA data the melting point for TlSnPS4 is 575 ± 5 °C. The title compound is not moisture sensitive and semi-conducting.

scholarly journals Die Kristallstrukturen von (1,5-Ditolylpentaazadienido)(triphenylphosphan)gold(I) und 1,5-Ditolyl-3-methylpentaazadien / The Crystal Structures of (1,5-Ditolylpentaazadienido)(triphenylphosphane)gold(I) and 1,5-Ditolyl-3-methylpentaazadien

1988 ◽  
Vol 43 (10) ◽  
pp. 1219-1223 ◽  
Author(s):  
Johannes Beck
Keyword(s):  
Nitrogen Atom ◽  
Crystal Structures ◽  
Phosphorus Atom ◽  
Gold Atom ◽  
Monoclinic Space Group ◽  
Orthorhombic Space Group ◽  
Space Group ◽  
Lattice Constants ◽  
Monomeric Complex ◽  
Single Bonds

PPh3Au(tolN5tol) is obtained by the reaction of PPh3Au+ClO4- with Tl(tolN5tol). It crystallizes in the monoclinic space group P21/c with the lattice parameters a = 1548.8(5), b = 1070.7(2), c = 1779.1(3) pm, β = 90.33(2)°, Z = 4. In the monomeric complex the gold atom is nearly linearcoordinated by the phosphorus atom of the PPh3 group and nitrogen atom N3 of the pentaazadienido ligand ( N3 - Au - P 178.4°). tolNN(NCH3)NNtol crystallizes in the orthorhombic space group Pccn with the lattice constants a = 2426.7(9), b = 469.3(2), c = 1195.3(4) pm. The unit cell contains four molecules, located on twofold axes. Due to the isolobality of the CH3 and the PPh3Au group, the two structures are closely related. Both contain the typical planar zig-zag chain of five nitrogen atoms with located double bonds N1-N2 and N4 - N5 (from 119.8 to 126.6 pm) and shortened single bonds N2 - N3 and N3 - N4 (132.7 to 140.0 pm).

scholarly journals Crystal Structures of Ethyl 4-(4-Florophenyl)-6-phenyl-2-substituted-3-pyridinecarboxylates

2014 ◽  
Vol 2014 ◽  
pp. 1-7
Author(s):  
ElSayed M. Shalaby ◽  
Aisha M. Moustafa ◽  
Adel S. Girgis ◽  
Aida M. ElShaabiny
Keyword(s):  
Crystal Structures ◽  
Piperidine Ring ◽  
Monoclinic System ◽  
Orthorhombic System ◽  
Space Group ◽  
Morpholine Ring

Three substituted pyridinecarboxylates were synthesized; (I) ethyl 2-bromo-4-4(fluorophenyl)-6-phenyl-3-pyridinecarboxylate, C20H15BrFNO2, (II) ethyl 4-(4-fluorophenyl)-2-(4-morpholinyl)-6-phenyl-3-pyridinecarboxylate, C24H23FN2O3, and (III) ethyl 4-(4-fluorophenyl)-6-phenyl-2-(1-piperidinyl)-3-pyridinecarboxylate, C25H25FN2O2. It was found that compound (I) belongs to the orthorhombic system with space group P212121, compound (II) to the monoclinic system with space group P21/c, and compound (III) to the monoclinic system with space group C2/c. The morpholine ring in (II) and piperidine ring in (III) have the shape of the distorted chair configuration.

The tetragermanatesA2Ge4O9(A= Na, K and Rb)

2013 ◽  
Vol 69 (9) ◽  
pp. 995-1001 ◽  
Author(s):  
Günther J. Redhammer ◽  
Gerold Tippelt
Keyword(s):  
Uniform Distribution ◽  
Crystal Structures ◽  
Membered Ring ◽  
Framework Structure ◽  
Alkali Cations ◽  
Tetrahedral Framework ◽  
Space Group ◽  
Main Building ◽  
Octahedral Sites

The crystal structures of three alkali tetragermanatesA2Ge4O9(A= Na, K and Rb) [namely disodium tetragermanate, Na2Ge4O9, dipotassium tetragermanate, K2Ge4O9, and dirubidium tetragermanate, Rb2Ge4O9] are trigonal (space groupP\overline{3}c1). The main building units are a three-membered ring of tetrahedra, oriented within the (001) plane and forming tetrahedral sheets. These sheets are connected to each other by two different regular isolated GeO6octahedraviacorner-sharing to build up a tetrahedral–octahedral framework. The alkali cations are located in cavities within this framework and are sevenfold coordinated. The increasing size of theA-site cation is accommodated by twist deformations of the tetrahedral rings and alterations in the Ge—O—Ge angles. With increasing size of theA-site cation, both the tetrahedral and octahedral sites become more regular, with slightly decreasing 〈Ge—O〉 distances from Na2Ge4O9to Rb2Ge4O9. This goes hand-in-hand with a more uniform distribution of bonds around theA-site cation. All these observations make Rb2Ge4O9the most regular member of thisA2Ge4O9octahedral–tetrahedral framework structure series.

The crystal structures of the 1:2 host:guest complexes of dicyclohexano-18-crown-6 (isomers A and B) with sodium and potassium phenoxide

1986 ◽  
Vol 64 (4) ◽  
pp. 816-823 ◽  
Author(s):  
Marie E. Fraser ◽  
Suzanne Fortier ◽  
André Rodrigue ◽  
John W. Bovenkamp
Keyword(s):  
Crown Ether ◽  
Crystal Structures ◽  
Metal Cation ◽  
Direct Methods ◽  
The Other ◽  
Full Matrix ◽  
Space Group ◽  
Elliptical Cavity ◽  
Cation Coordination ◽  
Sodium And Potassium

The crystal structures of the 1:2 host:guest complexes of dicyclohexano-18-crown-6 (isomer B) with potassium phenoxide and dicyclohexano-18-crown-6 (isomer A) with sodium phenoxide have been determined. The potassium phenoxide complex crystallizes in space group [Formula: see text] with a = 10.023(2), b = 11.238(2), c = 7.546(2) Å, α = 95.73(2), β = 103.04(2), γ = 92.03(2)°, and Z = 1. The sodium phenoxide complex crystallizes in space group P21/n with a = 19.185(12), b = 13.266(5), c = 13.038(5) Å, β = 96.55(4)°, and Z = 4. Both structures were solved by direct methods and refined by full matrix least-squares calculations to a residual, R, of 0.035. The host conformation as well as the metal cation coordination differ considerably in the two structures. In the potassium phenoxide complex, the two cations are related by symmetry and have, consequently, the same chemical environment. Each potassium is located approximately halfway between the plane formed by the crown ether oxygens and the phenoxide anions and is coordinated to four of the crown oxygens and to two phenoxide oxygens. The oxygens of the crown are found to outline an elliptical cavity and to lie approximately in a plane. In the sodium phenoxide complex, the two sodiums have different crystallographic and chemical environments. One sodium is coordinated to the six hexaether oxygens, with distances ranging from 2.36to2.84 Å, and to one of the phenoxide oxygens. The other sodium is coordinated to only one of the crown oxygens and to three of the phenoxide oxygens. The hexaether adopts a highly irregular conformation.

Sr5Al2Sb6 und Ba5In2Sb6: Zwei neue Zintlphasen mit unterschiedlichen Bänderanionen / Sr5Al2Sb6 and Ba5In2Sb6: Two New Zintl Phases with Different Chain Anions

1988 ◽  
Vol 43 (4) ◽  
pp. 463-466 ◽  
Author(s):  
Gerhard Cordier ◽  
Michael Stelter
Keyword(s):  
Zintl Phases ◽  
Orthorhombic System ◽  
Space Group ◽  
Lattice Constants

AbstractThe compound Sr5Al2Sb6 crystallizes in the orthorhombic system (space group Pnma (No. 62)) with the lattice constants: a = 1212.4(4) pm, b = 1034.1(4) pm, c = 1340.9(5) pm. AlSb4 tetrahedra are connected via common edges and corners to chains. Every second terminal Sb atom of the chain is connected to another Sb atom, such that end-on Sb2 groups and terminal Sb alternate. The compound Ba5In2Sb6 crystallizes in the orthorhombic system (space group Pbam (No. 55)). The lattice constants are: a = 1530.7(6) pm, b = 1335.8(5) pm, c = 478.6(2) pm. In the structure, InSb4 tetrahedra are connected via common corners and Sb2 groups to form double chains. Both compounds are classified as Zintl phases.

K2SiP2, ein Phosphidopolysilikat(IV) / K2SiP2, a Phosphidopolysilicate (IV)

1984 ◽  
Vol 39 (6) ◽  
pp. 736-738 ◽  
Author(s):  
Brigitte Eisenmann ◽  
Mehmet Somer
Keyword(s):  
Unit Cell ◽  
Compound K ◽  
Orthorhombic System ◽  
Space Group ◽  
Lattice Constants

AbstractThe new compound K2SiP2 crystallizes in the orthorhombic system , space group Ibam. The unit cell with the lattice constantsa = 1292.6(6) pm, b - 686.7(4) pm, c - 610.7(4) pmcontains 4 formula units. In the structure SiP4 tetrahedra form chains by sharing common edges. The [(SiP2)2-] strings are isosteric to the SiS2 molecules.

Sr3In2P4 und Ca3ln2As4, Zintlphasen mit Bänderanionen aus kanten-und eckenverknüpften InP4- bzw. InAs4-Tetraedern/ Sr3In2P4 and Ca3In2As4, Zintl Phases with Strings of InP4 and InAs4 Tetrahedra, Resp., Sharing Edges and Corners

1986 ◽  
Vol 41 (11) ◽  
pp. 1416-1419 ◽  
Author(s):  
Gerhard Cordier ◽  
Herbert Schäfer ◽  
Michael Stelter
Keyword(s):  
Zintl Phases ◽  
Orthorhombic System ◽  
Space Group ◽  
Lattice Constants ◽  
Partial Lattice ◽  
New Compounds

Abstract The new compounds Sr3In2P4 and Ca3In2As4 crystallize in the orthorhombic system , space group Pnnm (No. 58), with the following lattice constants:Sr3In2P4: a = 1632.3(6), b = 682.8(3), c = 428.9(2);Ca3In2As4: a = 1621.2(6), b = 659.5(3), c = 430.6(2).In the anionic partial lattice InP4 (InAs4) tetrahedra are connected by common edges and corners and form (InP23-)n ((In As23-)n) strings of alternating four-membered and eight-membered rings.

New Quaternary Selenoantimonates AHgSbSe3 (A = Rb, Cs): Synthesis, Structures and Optical Properties

1998 ◽  
Vol 547 ◽  
Author(s):  
Zhen Chen ◽  
Ru-Ji Wang ◽  
Jing Li
Keyword(s):  
Optical Properties ◽  
Alkali Metal ◽  
Crystal Structures ◽  
Diffuse Reflectance ◽  
Layered Materials ◽  
Band Gaps ◽  
Alkali Metal Cations ◽  
Monoclinic System ◽  
Orthorhombic System ◽  
Space Group

AbstractSolvothermal reactions in ethylenediamine have resulted in two quaternary mercury containing selenoantimonates: RbHgSbSe3 (I) and CsHgSbSe3 (II). Compound I crystallizes in monoclinic system, space group P2l/c (no. 14) with a = 7.758(2)Å, b = 11.234(2)Å, c = 8.849(2) Å, β = 106.60(3)°, V = 739.1(3)Å3, Z = 4. Compound II crystallizes in orthorhombic system, space group Cmcm (no. 63) with a = 4.444(1)Å, b = 15.514(6)Å, c = 11.261(7) Å, V = 776.4(6) Å3, Z = 4. Both compounds are layered materials and their crystal structures are closely related. Both contain layers of 2[HgSbSe3-] separated by alkali-metal cations A+ (Rb, Cs). Diffuse reflectance experiments show that both compounds are semiconductors with estimated band gaps of 1.7 eV for I and 1.6 eV for II, respectively.

Effect of Meta-Substitution on Solid State Geometry of N-(Aryl)-2,2,2-trichloro-acetamides, 3-XC6H4NH-CO-CCl3 and 3,5-X2C6H3NH-CO-CCl3 (X = Cl, CH3)

2007 ◽  
Vol 62 (1-2) ◽  
pp. 91-100
Author(s):  
Basavalinganadoddy Thimme Gowda ◽  
Jozef Kožíšek ◽  
Ingrid Svoboda ◽  
Hartmut Fuess
Keyword(s):  
Solid State ◽  
Crystal Structures ◽  
Nitro Group ◽  
Room Temperature ◽  
Asymmetric Unit ◽  
Strong Electron ◽  
Space Group ◽  
Lattice Constants ◽  
Crystal System ◽  
Electron Withdrawing Group

The crystal structures of N-(meta-substituted phenyl)-2,2,2-trichloro-acetamides such as N- (3-methylphenyl)-2,2,2-trichloro-acetamide, 3-CH3C6H4NH-CO-CCl3 (3MPTCA); N-(3-chlorophenyl)- 2,2,2-trichloro-acetamide, 3-ClC6H4NH-CO-CCl3 (3CPTCA); N-(3,5-dimethylphenyl)- 2,2,2-trichloro-acetamide, 3,5-(CH3)2C6H3NH-CO-CCl3 (35DMPTCA) and N-(3,5-dichlorophenyl)- 2,2,2-trichloro-acetamide, 3,5-Cl2C6H3NH-CO-CCl3 (35DCPTCA) have been determined at room temperature. The crystal system, space group, formula units and lattice constants (Å ) of the new structures are: 3MPTCA: orthorhombic, Pbca, Z = 8, a = 12.3199(11), b = 8.9719(8), c = 20.2058(15); 3CPTCA: orthorhombic, Fdd2, Z =16, a=19.285(4), b=40.765(8), c=5.5920(11); 35DMPTCA: triclinic, P1̄, Z = 2, a = 8.994(4), b = 9.9890(10), c = 14.760(5), α = 79.56(2)°, β = 73.32(3)°, γ = 86.47(2)°; and 35DCPTCA: orthorhombic, Pbca, Z = 8, a = 22.485(5), b=10.738(2), c=10.028(3). The compound 35DMPTCA has two molecules in its asymmetric unit, similar to o-NO2-, m-NO2- and p-CH3-substituted phenyl-trichloro-acetamides, while 3MPTCA, 3CPTCA and 35DCPTCA have one molecule each in their asymmetric units. The analysis of data indicates that the substitution of a strong electron withdrawing group such as a nitro group into PTCA at ortho or meta positions has a significant effect on the crystal parameters.

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