Kantenverknüpfte VO6-0ktaeder und PO4-Tetraeder in BaCa(VO)(PO4)2 / Edge-Connected VO6 Octahedra and PO4 Tetrahedra in BaCa(VO)(PO4)2

1997 ◽  
Vol 52 (5) ◽  
pp. 549-552 ◽  
Author(s):  
S. Meyer ◽  
Hk. Müller-Buschbaum
Keyword(s):  
Crystal Structure ◽  
Solid State ◽  
Melting Point ◽  
Single Crystals ◽  
Solid State Reactions ◽  
Monoclinic Symmetry ◽  
X Ray ◽  
Vanadyl Group ◽  
Symmetry Space ◽  
Symmetry Space Group

Abstract Single crystals of the new compound BaCa(VO)(PO4)2 have been prepared by solid state reactions below the melting point of the reactants in evacuated quartz tubes. X-ray investigations led to monoclinic symmetry, space group C2h5 - P21/c, a = 7.300(1), b = 7.053(1), c = 14.460(1) Å, β = 101,43(1)°, Z = 4. The crystal structure is characterized by layers of corner-and edge-connected PO4 tetrahedra and VO1+5 octahedra. There is an unusually short O(1)-O(4) distance in a VO6 octahedron of 2.44 Å associated with the sharing of edges with PO4 tetrahedra. The short V-O distance of 1.61 Å indicates a vanadyl group.

Ein Cadmium-Kupfer-Phosphat mit einfach überkappten trigonalen CdO6-Prismen-Netzen: Cd1.35Cu1.65(PO4)2

1996 ◽  
Vol 51 (2) ◽  
pp. 229-232 ◽  
Author(s):  
S. Münchau ◽  
Hk. Müller-Buschbaum
Keyword(s):  
Crystal Structure ◽  
Solid State ◽  
Melting Point ◽  
Single Crystals ◽  
Solid State Reactions ◽  
Monoclinic Symmetry ◽  
Space Group ◽  
Symmetry Space ◽  
Light Green ◽  
Symmetry Space Group

Abstract Single crystals of Cd1.35Cu1.65(PO4)2 have been prepared by solid state reactions below the melting point of the starting compounds. The light green crystals crystallize with monoclinic symmetry, space group C52h-P21/c , a = 9.062(2), b = 11.669(2), c = 5.950(2) Å , β = 97.88(2)°, Z = 4. Cd1.35Cu1.65(PO4)2 shows relationship to the mineral graftonite. The crystal structure is characterized by nets of corner connected Cd2O12 polyhedra. One point position is statistically occupied by Cd2+ and Cu2+ ions.

Isolierte MnCl6-Oktaeder im Oxohalogeno-Vanadat Ba5(Mg0,4Mn0,6)(V2O7)2MnCl6 / Isolated MnCl6 Octahedra in the Oxohalogeno Vanadate Ba5(Mg0,4Mn0,6)(V2O7)2MnCl6

1997 ◽  
Vol 52 (4) ◽  
pp. 457-461 ◽  
Author(s):  
R. Rettich ◽  
Hk. Müller-Buschbaum
Keyword(s):  
Crystal Structure ◽  
Solid State ◽  
Melting Point ◽  
Vanadium Oxide ◽  
Single Crystals ◽  
Solid State Reactions ◽  
Monoclinic Symmetry ◽  
Space Group ◽  
Symmetry Space ◽  
Symmetry Space Group

Single crystals of Ba5(Mg0,4Mn0,6)(V207)2MnCl6 have been prepared by solid state reactions of MgCO3, Mn2O3, V2O5 and BaCl2·2H2O below the melting point of BaCl2. The new vanadium oxide chloride crystallizeswith monoclinic symmetry, space group C42h-P2/c, a = 13.345(4), b = 5.711(2), c = 15.859(4) Å, β = 113.69(2)°, Z = 2. Special features of the crystal structure are isolated MnCl6 octahedra and layers created by divanadat groups and (Mg,Mn)O6 octahedra. The 2∞ [(Mg,Mn)V2O7] nets of Ba3(Mg0,4Mn0,6)(V2O7)2MnCl6 are discussed with respect to other oxohalogeno vanadates Containing divanadate groups.

Cd0,73Cu0,27V2O6: Eine Verbindung mit Branneritstruktur / Cd0 ,73Cu0,27V2O6: A Compound with Brannerite Structure

1994 ◽  
Vol 49 (7) ◽  
pp. 927-930 ◽  
Author(s):  
S. Münchau ◽  
Hk. Müller-Buschbaum
Keyword(s):  
Crystal Structure ◽  
Solid State ◽  
Single Crystals ◽  
Solid State Reactions ◽  
Monoclinic Symmetry ◽  
Space Group ◽  
X Ray ◽  
Jahn Teller ◽  
Symmetry Space ◽  
Symmetry Space Group

Abstract Single crystals of Cd0.73Cu0.27V2O6 were prepared by solid state reactions. X-ray investigations lead to monoclinic symmetry, space group C32h-C2/m , a = 9.339, b = 3.5604, c = 6.893 Å, β = 111.85°, Z = 2. It belongs to the Brannerite structure, showing a statistical distribution of Cd2+ and Cu2+ on one point position. The crystal structure of Brannerites is discussed with respect to the distorted O2- octahedra around V5+ and the influence of the Jahn-Teller active Cu2+ ion to the shortened M2+O6 octahedra.

Über das erste Oxopalladat-Arsenat: KMg3Pd(AsO4)3 / On the First Oxopalladat-Arsenate: KMg3Pd(AsO4)3

1995 ◽  
Vol 50 (6) ◽  
pp. 867-870 ◽  
Author(s):  
D. Frerichs ◽  
Hk. Müller-Buschbaum
Keyword(s):  
Crystal Structure ◽  
Solid State ◽  
Melting Point ◽  
Single Crystals ◽  
Crystal Chemistry ◽  
Point Of View ◽  
Solid State Reactions ◽  
Monoclinic Symmetry ◽  
Symmetry Space ◽  
Symmetry Space Group

Single crystals of KMg3Pd (AsO4)3 have been p repared by solid state reactions below the melting point of the reaction mixture. This compound crystallizes isotypic to the mineral Johilleriteo with monoclinic symmetry, space group C 2h6 -C 2/c , a = 12.098(3) Å, b = 12.853(5) Å , c = 6.688(3) Å, β = 112.92(3)°, Z = 4. The crystal structure is characterized by AsO4 tetrahedra, isolated planar but twisted PdO4 polygons, MgO6 octahedra and a 2+4+2- coordination of potassium . From the point of view of crystal chemistry KMg3Pd (AsO4)3 both belongs to the arsenates and oxopalladates(II).

scholarly journals Zur Kenntnis eines Barium-Oxoniobat-Tellurats: Ba2Nb2TeO10 / On a Barium-Oxoniobate-Tellurate: Ba2Nb2TeO10

1996 ◽  
Vol 51 (10) ◽  
pp. 1407-1410 ◽  
Author(s):  
B. Wedel ◽  
Hk. Müller-Buschbaum
Keyword(s):  
Crystal Structure ◽  
Solid State ◽  
Single Crystals ◽  
Solid State Reactions ◽  
Orthorhombic Symmetry ◽  
X Ray ◽  
Lattice Constants ◽  
Group D ◽  
Symmetry Space ◽  
Symmetry Space Group

Single crystals of Ba2Nb2TeO10) have been prepared by solid state reactions in air. X-ray investigations led to orthorhombic symmetry, space group D152h-Pbca, a = 7.242(4), b = 12.433(3), c = 9.932(3) Å. Z = 4. Nb5+ and Te6+ show octahedral coordination by O2- . The crystal structure is characterized by planes of edge- and corner-sharing NbO6- and TeO6octahedra. It is shown that in spite of nearly identical lattice constants of Ba2Nb2TeO10 with compounds of the composition M0,5BaNbTe2O9 the so far unknown crystals of these substances may not be derived from the Ba2Nb2TeO10 type.

Synthese und Struktureines Strontium-Vanadyl-Phosphats: Sr2(VO)(PO4)2 / Synthesis and Structure of a Strontium Vanadyl Phosphate: Sr2(VO)(PO4)2

1996 ◽  
Vol 51 (7) ◽  
pp. 929-933 ◽  
Author(s):  
C. Wadewitz ◽  
Hk. Müller-Buschbaum
Keyword(s):  
Solid State ◽  
Solid State Reactions ◽  
Vanadyl Phosphate ◽  
Monoclinic Symmetry ◽  
X Ray ◽  
Vanadyl Group ◽  
Dark Green ◽  
Symmetry Space ◽  
Oxygen Distance ◽  
Symmetry Space Group

Dark green single crystals of Sr2(VO)P2O8 have been prepared by solid state reactions in closed quartz tubes. X-ray investigations led to monoclinic symmetry, space group C2h6-I2/a, a = 6.744(4), b = 15.866(4), c = 7.032(2) Å, β = 115.41(2), Z = 4. Sr2(VO)P2O8 is isotypic to Sr2(VO)V2O8 and shows V4+ in split positions. The split positions are in non-centric octahedral coordination forming a short vanadium to oxygen distance typical for the vanadyl group. The crystal chemistry of the monovanadyl orthophate Sr2(VO)P2O8 is discussed considering related divanadyl phosphates.

Ein Beitrag zur Kristallchemie von Verbindungen mit Johillerit-Struktur: KCo3Cu(As2,58V0,42)O12 / On the Crystal Chemistry of Compounds with Johillerite Structure: KCo3Cu(As2,58V0,42)O12

1994 ◽  
Vol 49 (11) ◽  
pp. 1463-1466 ◽  
Author(s):  
D. Frerichs ◽  
Hk. Müller-Buschbaum
Keyword(s):  
Solid State ◽  
Melting Point ◽  
Single Crystals ◽  
Crystal Chemistry ◽  
Structure Type ◽  
Solid State Reactions ◽  
Tetrahedral Coordination ◽  
Monoclinic Symmetry ◽  
Symmetry Space ◽  
Symmetry Space Group

Single crystals of KCo3Cu(As2.58V0.42)O12 were prepared by solid state reactions below the melting point of the reaction mixture (K2CO3, CuO, COC2O4, V2O5 and 3 As2O5 · 5H2O). It crystallizes with monoclinic symmetry, space group C62h-C2/c, a = 12.207, b = 12.730, c = 6.811 Å, β = 113.69°, Z = 4. The structure type is characterized by isolated twisted-square CuO4-polygons, CoO6-octahedra and a special 4+4-coordination of the potassium ion. As5+ and V5+ are in tetrahedral coordination with a partly statistical distribution of these ions.

Kristallstrukturuntersuchung am Barium-Yanadyl-Vanadat: Ba2(VO)V2O8 / Crystal Structure Investigation of the Barium Vanadyl-Vanadate: Ba2(VO)V2O8

1996 ◽  
Vol 51 (4) ◽  
pp. 489-492 ◽  
Author(s):  
J. Feldmann ◽  
Hk. Müller-Buschbaum
Keyword(s):  
Crystal Structure ◽  
Solid State ◽  
Single Crystals ◽  
Structure Type ◽  
Solid State Reactions ◽  
Tetrahedral Coordination ◽  
Structure Investigation ◽  
Monoclinic Symmetry ◽  
Symmetry Space ◽  
Symmetry Space Group

Abstract Single crystals of Ba2(VO)V2O8 have been prepared by solid state reactions of Ba2V2O7, V2O3 and V2O5 in sealed silica tubes. This compound crystallizes with monoclinic symmetry, space group C22 -P21, a = 8.1174(9), b = 5.9699(9), c = 9.2903(9) Å , β = 113.94(1)°, Z = 2. V 5+ shows tetrahedral coordination. V 4+ inside 1∞ [V (3)O4] chains is characterized by a square pyramidal coordination with a short apical V-O distance of 1.6 Å typically for vanadyl groups. Ba2(VO)V2O8 represents a new structure type and is not isotypic to Sr2(VO)V2O8.

Kurze O-O-Abstände einer gemeinsamen Polyederkante bei Verknüpfung von PO4-Tetraedern mit VO6-Oktaedern im Vanadyl-Orthophosphat CaNi(VO)(PO4)2 / Short O-O Distances in Edge Sharing PO4 Tetrahedra and VO6 Octahedra of the Vanadyl- Orthophosphate CaNi(VO)(PO4)2

1997 ◽  
Vol 52 (8) ◽  
pp. 981-984 ◽  
Author(s):  
S Meyer ◽  
Hk Müller-Buschbaum
Keyword(s):  
Crystal Structure ◽  
Melting Point ◽  
Solid State Reactions ◽  
Orthorhombic Symmetry ◽  
Oxide Mixture ◽  
X Ray ◽  
Vanadyl Group ◽  
Group D ◽  
Symmetry Space ◽  
Symmetry Space Group

Abstract Single crystals of the new compound CaNi(VO)(PO4)2 have been prepared by solid state reactions below the melting point of the oxide mixture in evacuated quartz tubes. X-ray investigations led to orthorhombic symmetry, space group D2h16-Pnma, a =14.113(1), b =6.408(1), c = 7.364(1) Å, Z = 4. The crystal structure shows 1∞[NiO4] and 1∞[VO6P2O3] polyhedra chains closely related to analogous chains in the isotypic compound CdV2O(PO4)2. The short V -O distance of 1.66 Å indicates a vanadyl group as the main difference to CdV2O(PO4)2. The short O-O distance of 2,395 Å of the edge-sharing PO4 tetrahedra and VO6 octahedra is discussed.

Ba4Mn2Ag2O(As04)4 , ein Barium-Mangan-Oxid-Arsenat mit nichtlinearen O-Ag-O-Hanteln / Ba4Mn2Ag2O(AsO4)4, a Barium Manganese Oxide-Arsenate Showing Nonlinear O-Ag-O Dumbbells

1998 ◽  
Vol 53 (5-6) ◽  
pp. 512-516 ◽  
Author(s):  
M. Staack ◽  
Hk. Müller-Buschbaum
Keyword(s):  
Crystal Structure ◽  
Solid State ◽  
Bond Angle ◽  
Magnetic Measurements ◽  
Solid State Reactions ◽  
Metallic Silver ◽  
Monoclinic Symmetry ◽  
X Ray ◽  
Symmetry Space ◽  
Symmetry Space Group

Abstract Single crystals of Ba4Mn2Ag2O(AsO4)4 have been prepared by solid state reactions using metallic silver as reactant. X-ray techniques led to monoclinic symmetry, space group D2h-P2,/m, a = 8.739(2), b = 5.912(1), c = 9.440(2) Å, β = 115.21(1)°, Z = 1. The crystal structure is characterized by O-Ag-O dumbbells, bond angle = 165,3°, containing one oxygen atom not associated with the arsenate groups. Considering these facts Ba4Mn2Ag2O(AsO4)4 may be seen as an oxide-arsenate or an oxoargentate(I)-arsenate. Assuming the oxidation state +II for manganese, as confirmed by magnetic measurements, the compound has an oxygen deficite which was accounted for by a split position model.

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