Search
Go toArchive
Browse byFacets
Bookbag ( 0 )
'copper' in keywords Facet   Publication Year 1995  [X]
Facet   section ZfN Section B:Volume 050  [X]
Modify Search
Results  14 Items
Sorted by   
Section
expandZfN
expandZfN Section A
collapseZfN Section B
Volume 050[X]
expandZfN Section C
Publication Year
1995[X]
1Author    Ch LangRequires cookie*
 Title      
 Abstract    Single crystals of LiBa2Cu30 6 have been pre­ pared by recrystallization from melts in a stream of dry Argon as well as by spontaneous CO 2-LASER heating. It crystallizes with orthorhom bic symmetry, space group -Fmmm, a = 8,219(2), b = 11,520 (2), c = 14,284(3) A, Z = 8. The crystal structure is isotypic to NaBa2Cu30 6. 
  Reference    Z. Naturforsch. 50b, 681—683 (1995); eingegangen am 19. September 1994 
  Published    1995 
  Keywords    Lithium, Barium, Copper, Oxide 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/50/ZNB-1995-50b-0681_n.pdf 
 Identifier    ZNB-1995-50b-0681_n 
 Volume    50 
2Author    H. Szillat, Hk Müller-BuschbaumRequires cookie*
 Title    Synthesis and Crystal Structure of (Cu,Zn)3 7 5 Mo30 12  
 Abstract    Single crystals of (Cu,Zn)3 75Mo30 12 have been prepared by crystallization from melts and investigated by X-ray diffractometer techniques. (Cu,Zn)3 75Mo3Oi2 crystallizes orthorhom-bically, space group D^-P212,21, Z = 4, a = 17.947(9), b = 5.092(3), c = 10.685(5) A. It is isotypic to Cu385Mo30 12. All molybdenum atoms are tetrahedrally coordinated by oxygen atoms. There are layers of C u 0 6 and Z n 0 6 octahedra, while other metal sites are occupied by copper in a deformed prismatic coordination with one oxygen atom at a remarkably greater distance from copper than the other five. Some of the zinc atoms occupy positions in chains of face-sharing octahedra with an occupancy factor of 0.75. The crystal structure is discussed with respect to the isotypic compound Cu385Mo30 12 and compounds of the type CuLnMo20 8. 
  Reference    Z. Naturforsch. 50b, 247—251 (1995); eingegangen am 13. September 1994 
  Published    1995 
  Keywords    Crystal Structure, Copper, Molybdenum, Zinc, Oxide 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/50/ZNB-1995-50b-0247.pdf 
 Identifier    ZNB-1995-50b-0247 
 Volume    50 
3Author    H. Szillat, Hk Müller-BuschbaumRequires cookie*
 Title    Uber das Oxomolybdat AgKCu3Mo4Oi6 mit Silber in siebenfacher Koordination About the Oxomolybdate AgKCu3Mo4O i6 with Silver in Seven-Fold Coordination  
 Abstract    Single crystals of AgKCu3Mo40 16 have been prepared by crystallization from melts and investigated by X-ray diffractometer techniques. This compound crystallizes with monoclinic symmetry, space group C |h-P 2 Je, a = 5.056(1), b = 14.546(4), c = 19.858(9) Ä, ß = 86.64(5)°, Z = 4. The crystal structure of AgKCu3Mo40 16 is closely related to K2Cu3Mo40 16 showing ribbons of edge-sharing C u 0 6 and AgÖ7 polyhedra. The ribbons are linked by tetrahedrally coordinated molybdenum and K2O 10 groups. Another kind of M o 0 4 tetrahedra occupies the cavities inside the ribbons. The crystal structure and the coordination of silver, copper, potas­ sium and molybdenum by oxygen are discussed with respect to K2Cu3Mo40 16. 
  Reference    Z. Naturforsch. 50b, 252—256 (1995); eingegangen am 19. September 1994 
  Published    1995 
  Keywords    Crystal Structure, Copper, Silver, Molybdenum, Potassium 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/50/ZNB-1995-50b-0252.pdf 
 Identifier    ZNB-1995-50b-0252 
 Volume    50 
4Author    H. Szillat, Hk Müller-BuschbaumRequires cookie*
 Title    Zur Kristallchemie eines neuen Oxomolybdats: Cu2YbMo30 12 On the Crystal Chemistry of a New Molybdenum Oxide: Cu2YbM o30 12  
 Abstract    Single crystals of Cu2YbMo30 12 have been prepared by crystallization from melts and investigated by X-ray diffractometer techniques. Cu2YbMo30 12 crystallizes with monoclinic symmetry (space group C 2h -P 12i/m l, a = 5.162(2), b = 10.885(4), c = 8.699(4) A. ß -95.73(7)°, Z = 2), forming a new structure type. Typical features are layers of C u 0 6 octahedra, connected via corners and edges. These layers are linked by molybdenum and ytterbium ions along [001]. The crystal structure as well as the coordination of copper, ytterbium and molybdenum and the oxidation states of copper and molybdenum are discussed with respect to the related but not isotypic compound (Cu,Zn)3 75Mo30 12. 
  Reference    Z. Naturforsch. 50b, 257—260 (1995); eingegangen am 19. September 1994 
  Published    1995 
  Keywords    Crystal Structure, Copper, Molybdenum, Ytterbium, Oxide 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/50/ZNB-1995-50b-0257.pdf 
 Identifier    ZNB-1995-50b-0257 
 Volume    50 
5Author    H. Szillat, Hk Müller-BuschbaumRequires cookie*
 Title    Synthese und Kristallstruktur eines Oxoantimonats mit Verwandtschaft zum Delafossit-Typ: Cu3MgSbl940 6 Synthesis and Crystal Structure of an Oxoantimonate with Relationship to the Delafossite Type: Cu3MgSbi 40 6  
 Abstract    Single crystals of Cu3MgSb140 6 have been prepared by crystallization from melts and investigated by X-ray diffractometer techniques. Cu^MgSb] 40 6 crystallizes trigonally, space group C 3v — R3/c, a = 5.348(1), c = 34.482(8) A, Z = 6, with a Delafossite related new structure, characterized by layers containing S b 0 6 and M g06 octahedra. These layers are connected by O -C u -O dumb-bells. The crystal structure is discussed with respect to the Delafossite type. 
  Reference    Z. Naturforsch. 50b, 261—264 (1995); eingegangen am 26. September 1994 
  Published    1995 
  Keywords    Crystal Structure, Copper, Magnesium, Antimony, Oxide 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/50/ZNB-1995-50b-0261.pdf 
 Identifier    ZNB-1995-50b-0261 
 Volume    50 
6Author    JanKarsten Schaefer, BluhmRequires cookie*
 Title    C  
 Abstract    uT m 2[ B 20 5] 2: D as erste "M etaborat" mit einem x [ B 20 5] 4 -Anion CuTm2[B20 5]2: The First " Metaborate" with a ^ [ B ^ s ] 4 -Anion Single crystals o f the compound CuTm2[B 20 3]2 were obtained by a B20 3 flux technique. The compound contains a hitherto unknown metaborate anion with the formula ^ [ ^ O s ] 4-. It crystallizes in the monoclinic space group C|h-P2!/c with a = 452.18(7); b = 720.0(2); c = 929.2(5) pm; ß -90.16(5)°; Z = 2. The metaborate layers consists of four and eight membered rings of edge-sharing B 0 4-tetrahedra resembling the complex anion in the isotypic gadolinite structure of F e Y 2[B eS i0 3]2. The layers are connected via copper-centered elongated oxygen octahedra and slightly distorted thulium-centered tetragonal oxygen antiprisms. 
  Reference    Z. Naturforsch. 50b, 630—634 (1995); eingegangen am 2. August/11. November 1994 
  Published    1995 
  Keywords    Copper, Thulium, Borate, Synthesis, Crystal Structure 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/50/ZNB-1995-50b-0630.pdf 
 Identifier    ZNB-1995-50b-0630 
 Volume    50 
7Author    H. Szillat, Hk Müller-BuschbaumRequires cookie*
 Title    On the Oxocuprate (C u,C o)375Mo30 12  
 Abstract    Single crystals of (C u,C o)3 7?Mo30 12 have been prepared by recrystallization from melts and investigated by X-ray diffractometer techniques. TTie compound crystallizes with ortho-rhombic symmetry, space group D'2 6 h-P n m a , a = 5.092(1), b = 10.624(3), c = 17.804(4) A, Z = 4 and is isotypic to NaCo2.3iMo30 12. The crystal structure is discussed and it is shown, that the trigonal prismatically coordinated copper positions are occupied in a different m an­ ner. One of the alternate sites is beside the centre of the prisms, and the other one is shifted towards one of the faces of the rectangular prism. This detail may be interpreted by assigning the valance states C u1 and Cu11. The M 0 6 octahedra are occupied statistically by copper and cobalt. 
  Reference    Z. Naturforsch. 50b, 707—711 (1995); eingegangen am 10. O ktober 1994 
  Published    1995 
  Keywords    Crystal Structure, Copper, Cobalt, Molybdenum, Oxide 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/50/ZNB-1995-50b-0707.pdf 
 Identifier    ZNB-1995-50b-0707 
 Volume    50 
8Author    H. Szillat, Hk Müller-BuschbaumRequires cookie*
 Title    Zur Darstellung und Kristallstruktur eines neuen Kupfer-Antimon-Oxomolybdats: CuSbMo20 8 On the Synthesis and Crystal Structure of a New Copper Antimony Oxomolybdate: CuSbMo20 8  
 Abstract    Single crystals of the hitherto unknown com pound CuSbMo2O s were prepared by recrys­ tallization from melts in closed copper tubes and investigated by X-ray diffractometer techni­ que. CuSbMo^Os crystallizes in a new structure type with monoclinic symmetry, space group q ? h-I 1 2 /a l, a = 5.554(2), b = 4.916(1), c = 21.519(4) Ä, ß = 93.42(3)°, Z = 4. The crystal structure shows Sb111 in a one-sided coordination by four oxygen. Molybdenum shows the rare octahedral coordination by oxygen. M o 0 6 and C u 0 6 octahedra form triple layers stacked and connected by Sb ions along [001], 
  Reference    Z. Naturforsch. 50b, 717—720 (1995); eingegangen am 12. O ktober 1994 
  Published    1995 
  Keywords    Crystal Structure, Copper, Antimony, Molybdenum, Oxide 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/50/ZNB-1995-50b-0717.pdf 
 Identifier    ZNB-1995-50b-0717 
 Volume    50 
9Author    J. Schaefer, K. BluhmRequires cookie*
 Title    Synthese und Kristallstruktur von CuLn2[B20 5]2 (Ln = Er3*, Lu3+): zwei Kupferlanthanoidborate m it^ [B 20 5 ]4_-A nionen Synthesis and Crystal Structure of CuLn2[B20 5]2 (Ln = E r3+, Lu3+): Two Copper Lanthanoid B orates with 2.[B20 5]4~-Anions  
 Abstract    Single crystals of the new com pounds CuLn2[B20 5]2 (Ln = Er3+(I), Lu3+(II)) were ob­ tained by a B9O 3 flux-technique. They crystallize in the space group C ih -P 2 \lc with I: a = 453.14(6); b = 721.94(5); c = 929.5(4) pm; ß = 90.01(3)°; Z = 2 und II: a = 451.4(4); b = 718.3(1); c = 928.1(3) pm; ß = 90.00(6)°; Z = 2. The compounds are isotypic to CuTm2[B20 5 ] 2 as well as to the mineral Gadolinite (FeY 2 [B eSi0 5 ]2) and exhibit layer like 2.[B20 5]4 --anions consisting of edge sharing B 0 4 -tetrahedra, which form four-and eight-membered rings. The borate anions are separated by layers of elongated C u 0 6-octahedra and slightly distorted tetragonal L n 0 8-antiprisms. 
  Reference    Z. Naturforsch. 50b, 1141—1145 (1995); eingegangen am 19. Januar 1995 
  Published    1995 
  Keywords    Copper, Erbium, Lutetium, Borate, Crystal Structure 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/50/ZNB-1995-50b-1141.pdf 
 Identifier    ZNB-1995-50b-1141 
 Volume    50 
10Author    Sabine Münchau, Karsten BluhmRequires cookie*
 Title    Zur Synthese und Kristallstruktur von Kupfercadmiumpyroboratoxid: Cu2Cd(B20 5) 0 Synthesis and Crystal Structure of Copper Cadmium Pyroborate Oxide: Cu2Cd(B20 5) 0  
 Abstract    Single crystals of the new compound Cu2C d(B20 5) 0 have been prepared by B 20 3/V 20 5 flux technique in a closed silver tube. Their structure is isotypic with Cu2C o(B 20 5) 0 but its preparation is quite different. X-ray investigations on single crystals led to the space group C |h-P 2 !/c (Nr. 14), a = 339.9(2); b = 1509.8(2); c -927,0(1) pm; ß = 93.19(1)°; Z -4. The structure contains isolated B 2O s groups and oxygen that is not coordinated to boron. Cad­ mium is octahedrally coordinated by oxygen, while copper exhibits a nearly square planar or a fivefold pyramidal coordination. 
  Reference    Z. Naturforsch. 50b, 1151 (1995); eingegangen am 19. Januar 1995 
  Published    1995 
  Keywords    Copper, Cadmium, Pyroborate, Oxide, Crystal Structure 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/50/ZNB-1995-50b-1151.pdf 
 Identifier    ZNB-1995-50b-1151 
 Volume    50 
11Author    VerbindungC., S. Münchau, Hk Müller-BuschbaumRequires cookie*
 Title    Synthese und Kristallstruktur einer mit dem Johillerit verwandten  
 Abstract    Single crystals of C dC u^M gx.5Pbo.5V30 12 have been prepared in closed steel tubes using V 20 5 as a flux. The orange crystals show monoclinic symmetry, space group C2h-C 2 /c , a = 12.417(5), b = 12.983(6), c = 6.911(3) Ä , ß = 113.02(1)°, Z = 4. CdCu1.5Mg1.5PbojV30 12 reveals a relationship to the Johillerite type, but it is characterized by an additional point position for cadmium, situated betw een the square planar C u 0 4 polygons of the Johillerite structure. 
  Reference    Z. Naturforsch. 50b, 1158—1162 (1995); eingegangen am 22. D ezem ber 1994 
  Published    1995 
  Keywords    Cadmium, Copper, Magnesium, Lead, Vanadium, Oxide, Crystal Structure 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/50/ZNB-1995-50b-1158.pdf 
 Identifier    ZNB-1995-50b-1158 
 Volume    50 
12Author    J. Feldmann, Hk Müller-BuschbaumRequires cookie*
 Title    Kristallstrukturuntersuchung an einem bismuthaltigen Hollandit: Crystal Structure Investigation of the Bismuth Containing Hollandite: Bij 9Cu4V40 16  
 Abstract    Single crystals of B^ 9Cu4V 4O i6 have been prepared by quenching of CO2-LA SER heated samples. They were investigated by X-ray techniques. The compound^ crystallizes with tetra­ gonal symmetry, space group C4h-I 4 /w , a = 9.945(2) A, c = 2.915(3) A, Z = 1, and is isotypic to the mineral Hollandite. B^ 9Cu4V4O i6 is the first Hollandite with a statistical distribution of vanadium and copper in the network o f octahedra. Calculations of the Coulomb terms of lattice energy led to a distance o f bismuth to the lone pair of 1.07 A. Considering the lone pair as part of the coordination sphere of Bi3+ a square pyramidal polyhedron is obtained. 
  Reference    Z. Naturforsch. 50b, 1163—1166 (1995); eingegangen am 22. D ezem ber 1994 
  Published    1995 
  Keywords    Bismuth, Copper, Vanadium, Oxide, Crystal Structure 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/50/ZNB-1995-50b-1163.pdf 
 Identifier    ZNB-1995-50b-1163 
 Volume    50 
13Author    Karsten Busche, BluhmRequires cookie*
 Title    Silke  
 Abstract    The compound Cu2 Z n(B 2 0 s) 0 was prepared by using a B 2 0 3 flux technique, and single crystals were investigated by X-ray diffraction (monoclinic symmetry, space group C2 h-P 2 i/c). The structure is isotypic to Cu2 C o(B 2 0 5) 0 with lattice parameters a = 327.38(2), b = 1479.4(3), c = 915.39(13), ß = 95.794(11)°, Z = 4, but with the significant difference that zinc is penta-coordinated by oxygen. Copper exhibits a nearly square planar or a square pyramidal coordi­ nation, respectively. The structure contains isolated B2 0 ? units and oxygen which is not coordinated to boron. Zur Synthese und Kristallstruktur von Kupferzinkpyroboratoxid Cu2Zn(B20 5) 0 
  Reference    Z. Naturforsch. 50b, 1854—1858 (1995); eingegangen am 17. Mai 1995 
  Published    1995 
  Keywords    Copper, Zinc, Pyroborate, Oxide, Crystal Structure 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/50/ZNB-1995-50b-1854.pdf 
 Identifier    ZNB-1995-50b-1854 
 Volume    50 
14Author    H. Szillat, Hk Müller-BuschbaumRequires cookie*
 Title    Uber das Erdalkalimetall-Lanthanoid  
 Abstract    Kupfer-Oxomolybdat (Cu0,22Mg0 ,78)BaNd2Mo4O 16 The Alkaline Earth R are E arth Copper-Oxomolybdate (C u 0 . 2 2 M g 0 . 7 8) B a N d 2 M o 4 O 1 6 Single crystals of (Cu0.22Mg0 78)B aN d2M o4O i6 have been prepared by crystallization from melts and investigated by X-ray methods. The compound crystallizes monoclinically, space group C ^ -C 1 2 /cl, Z = 4, a = 5.351(1), b = 12.891(2), c = 19.391(4) Ä, ß = 90.899(14)° and is isotypic to CuKHo2M o40 16. The crystal structure is dominated by B aO 10 and N d 0 8 poly-hedra forming a three-dimensional polyhedra network, which is filled by axially distorted (C u,M g)O fi octahedra and M o 0 4 tetrahedra. 
  Reference    Z. Naturforsch. 50b, 577 (1995); eingegangen am 4. Oktober 1994 
  Published    1995 
  Keywords    Crystal Structure, Copper, M agnesium, Barium, Neodymium, Molybdenum, Oxide 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/50/ZNB-1995-50b-0577.pdf 
 Identifier    ZNB-1995-50b-0577 
 Volume    50 
Disclaimer   ★    Pivacy Policy   ★    Contact

Creative Commons License