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261Author    Tsutomu Okuda, Yoshihiro Kinoshita, Hiromitsu Terao, Koji YamadaRequires cookie*
 Title    Structure and Bonding of Bromoantimonate (III) Complexes with Unusual Valency by Means of NQR and Powder X-Ray Diffraction  
 Abstract    NQR and powder X-ray diffraction were observed for several bromoantimonate (III) complexes which contain C"H2n+ jNF^ (n = 1 -3) or (C"H2lt + 1)2N H 2 (n = 1 -4) as a cation. The bond character, anion structure, crystal structure, and phase transition are discussed on the basis of the three-center-four-electron bond. A good correlation was found between the halogen NQR frequency and the Sb-X bond length. 
  Reference    Z. Naturforsch. 49a, 185—192 (1994); received July 23 1993 
  Published    1994 
  Keywords    81Br NQR, Temperature dependence, Phase transition, Crystal structure 
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 TEI-XML for    default:Reihe_A/49/ZNA-1994-49a-0185.pdf 
 Identifier    ZNA-1994-49a-0185 
 Volume    49 
262Author    Jacek ZaleskiRequires cookie*
 Title    Crystal Structure and Phase Transitions of [C(NH2)3]3Sb2C l9 * 0.9 H 20 A dam Pietraszko  
 Abstract    The room temperature structure of [C(NH2)3]3Sb2C l9 ■ 0.9 H 20 (GNCA) was solved. It crystal­ lizes in the monoclinic C2/c space group with a = 15.275, b = 8.794, c = 17.904 (in Ä), ß = 96.40°, V = 2390 Ä 3, Z = 4. Refinement of the atomic parameters by a least squares methods gave R = 0.042, wR = 0.039 for 1958 reflections with F>4ct(F). The structure consists of polyanionic (Sb2Cl|_)n layers built of deformed corner connected SbX^-octahedra. Two crystallographically inequivalent guanidinium cations are present, one situated between polyanionic layers, the other one together with a disordered water molecule inside cavities formed by polyanions. Temperature X-ray scattering experiments together with DSC studies were carried out above room temperature. Temperature dependence of the lattice parameters between 300 K and 380 K was determined and a phase transition of mixed order at 364 K was revealed. 
  Reference    Z. Naturforsch. 49a, 895—901 (1994); received June 7 1994 
  Published    1994 
  Keywords    Guanidinium, Chloroantimonate, Crystal structure, Phase transition, DSC 
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 TEI-XML for    default:Reihe_A/49/ZNA-1994-49a-0895.pdf 
 Identifier    ZNA-1994-49a-0895 
 Volume    49 
263Author    Hiroyuki Ishida, Hironobu Maeda, Akiko Hirano, Tamotsu Fujimoto, Yoshihiro Kubozono, Setsuo Kashino, Shuichi EmuraRequires cookie*
 Title    E X A F S S tu d y o n th e P h a s e T r a n s itio n ( P h a s e a ' -5) in C H 3 N H 3 I  
 Abstract    The local structure of CH3NH3I around the I" ion in Phase a 'and 8 was studied by iodine K-edge EXAFS. The crystal structure in Phase a ' was redetermined by single crystal X-ray diffraction. The Debye-Waller factor <r(2) derived from EXAFS spectra shows an anomalous behavior around the order-disorder transition temperature from Phase 8 to a '. The phase transition has been interpreted as the disordering process which involves not only the H atoms but also the C atoms in the cation. 
  Reference    Z. Naturforsch. 50a, 876—880 (1995); received June 16 1995 
  Published    1995 
  Keywords    Crystal structure, EXAFS, Phase transition, X-ray diffraction 
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 TEI-XML for    default:Reihe_A/50/ZNA-1995-50a-0876.pdf 
 Identifier    ZNA-1995-50a-0876 
 Volume    50 
264Author    Hiroyuki Ishida, Hiroshi Ono, Ryuichi IkedaRequires cookie*
 Title    Crystal Structure of the High-temperature Solid Phases of Choline Tetrafluoroborate and Iodide  
 Abstract    The crystal structure of the highest-and second highest-temperature solid phases of choline tetrafluoroborate and iodide was determined by X-ray powder diffraction. The structure in the highest-temperature phase of both salts is NaCl-type cubic (a = 10.16(2) Ä, Z = 4 for tetrafluorobo-rate; a = 10.08(2) A, Z = 4 for iodide). The second highest-temperature phase of tetrafluoroborate and iodide is CsCl-type cubic (a = 6.198(6) Ä and Z = 1) and tetragonal (a = 8.706(2) A, c = 6.144(6) Ä, and Z = 2), respectively. DSC was carried out for the iodide, where the presence of three solid-solid phase transitions was confirmed. Enthalpy and entropy changes of these transitions were evaluated. 
  Reference    Z. Naturforsch. 52a, 679—680 (1997); received June 17 1997 
  Published    1997 
  Keywords    Crystal structure, Powder X-ray diffraction, Phase transition 
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 TEI-XML for    default:Reihe_A/52/ZNA-1997-52a-0679_n.pdf 
 Identifier    ZNA-1997-52a-0679_n 
 Volume    52 
265Author    J. Pirnat, Z. Trontelj, Z. Jagličić, K. Lutar, H. BorrmannRequires cookie*
 Title    Arsenic NQR in the Paramagnetic Complex Co(AsF 6 ) 2 -2AsF 3  
 Abstract    Arsenic NQR in Co(AsF 6) 2 .2AsF 3 reveals three lines: one near 122 MHz and two near 50 MHz. Relations of the spectral lines to the structure and to thermal vibrations are discussed. Possible influence of paramagnetic Co is examined. 
  Reference    Z. Naturforsch. 55a, 212—214 (2000); received October 13 1999 
  Published    2000 
  Keywords    Co(AsF 6 ) 2, Complex, NQR, Paramagnet, Crystal Structure 
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 TEI-XML for    default:Reihe_A/55/ZNA-2000-55a-0212.pdf 
 Identifier    ZNA-2000-55a-0212 
 Volume    55 
266Author    Hideta Ishihara, Keizo Horiuchi, ThorstenM. Gesing, Shi-Qi Dou, J.-Christian Buhl, Hiromitsu TeraoRequires cookie*
 Title    I NQR and Crystal Structure Studies of [N(CH 3 ) 4 ] 2 CdI 4  
 Abstract    The temperature dependence of 127 1 NQR and DSC as well as the crystal structure at room temperature of the title compound were determined. This compound shows a first-order phase transition of an order-disorder type at 245 K. Eight 127 I(i^i: m = ±5 <-+ ±|) NQR lines of 79. corresponding eight 127 I(^ 2 : m = ±| <-» • ±|) NQR lines were observed at liquid nitrogen temperature. Three 127 I(^i) NQR lines wfth an intensity ratio of 1:1:2 in the order of decreasing frequency were observed just above the transition point and two NQR lines except for the middle-frequency line disappeared around room temperature. This temperature behavior of NQR lines is very similar to that observed in [N(CH 3)4] 2 Hgl4. Another first-order phase transition takes place at 527 K. The structure of the room-temperature phase was redetermined: orthorhombic, Pnma, Z = 4, a = 1342.8(3), b = 975.7(2), c = 1696.5(3) pm. The NQR result of three lines with an intensity ratio of 1:1:2 is in agreement with this structure. The thermal displacement parameters of atoms in both cations and anions are large. 
  Reference    Z. Naturforsch. 55a, 225—229 (2000); received October 13 1999 
  Published    2000 
  Keywords    NQR, DSC, Crystal Structure, Phase Transition 
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 TEI-XML for    default:Reihe_A/55/ZNA-2000-55a-0225.pdf 
 Identifier    ZNA-2000-55a-0225 
 Volume    55 
267Author    Hideta Ishihara, Keizo Horiuchi, V. G. Krishnan, Ingrid Svoboda, Hartmut FuessRequires cookie*
 Title    Isolated versus Condensed Anion Structure VI: X-ray Structure Analysis and 81 Br NQR of Guanidinium Pentabromodicadmate(II), [C(NH 2 ) 3 ]Cd 2 Br 5 , fns-Hydrazinium Pentabromocadmate(II), [H 2 NNH 3 ] 3 CdBr 5 , and fo's-Hydrazinium Tetrabromocadmate(II)-Tetra Hydrate, [H 2 NNH 3 ] 2 CdBr 4 -4H 2 0  
 Abstract    The structure of the condensed bromocadmate anions in [C(NH 2) 3 ]Cd 2 Br 5 (1) and [H 2 NNH 3 ] 3 CdBr 5 (2) were studied at room temperature by X-ray diffraction. (1) crystallizes with double-chains bridged by Br atoms (orthorhombic, Pmmn, Z= 2, a = 1394.0(5), b = 394.5(1), c = 1086.9(5) pm). This chain structure was not described previously. (1) shows three 8 'Br NQR lines at temperatures between 77 and 323 K. Structural phase transitions take place at 283 K and at 535 K. (2) crystallizes with Br bridged zigzag-chains (monoclinic, P2[, Z=2,a = 943.1(1), b = 778.8(2), c = 942.0(2) pm, ß = 102.10(2)°) and shows a first-order phase transition around 304 K with a large thermal hysteresis. Below the transition point five 81 Br NQR lines are observed at temperatures between 122 and 304 K, and above the transition point four 81 Br NQR lines at tem-peratures between 288 and 353 K. Two 81 Br NQR lines are observed in [H 2 NNH 3 ] 2 CdBr 4 -4H 2 0 (3) at temperatures between 77 and around 320 K with positive temperature coefficients. 
  Reference    Z. Naturforsch. 55a, 390—396 (2000); received November 19 1999 
  Published    2000 
  Keywords    NQR, DSC, Crystal Structure, Phase Transition, Bromocadmate 
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 TEI-XML for    default:Reihe_A/55/ZNA-2000-55a-0390.pdf 
 Identifier    ZNA-2000-55a-0390 
 Volume    55 
268Author    Hiroyuki Ishida, Setsuo Kashino, Ryuichi IkedaRequires cookie*
 Title    Crystal Structure of Trimethylammonium Tetrafluoroborate in Three Solid Phases  
 Abstract    The crystal structure of (CH 3) 3 NHBF 4 was studied in three solid phases by X-ray diffraction techniques. The structures of the ionic plastic phase (Phase I) stable above 453 K and Phase II between 384 and 453 K are CsCl-type cubic (a = 5.772(4) Ä) and tetragonal (a = 9.815(5) and c = 6.895(5) A), respectively. The room temperature phase (Phase III) forms a monoclinic lattice (space group P2,/m, a = 5.7017(8), b = 8.5724(9), c = 7.444(1) Ä, and ß = 102.76(1)°). BF 4 ~ ions in this phase were shown to be disordered in four orientations. 
  Reference    Z. Naturforsch. 55a, 765—768 (2000); received June 28 2000 
  Published    2000 
  Keywords    Crystal Structure, X-ray Diffraction, Ionic Plastic Phase, Disorder 
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 TEI-XML for    default:Reihe_A/55/ZNA-2000-55a-0765.pdf 
 Identifier    ZNA-2000-55a-0765 
 Volume    55 
269Author    Hideta Ishihara, Toshiya Okajima, Keizo Horiuchia, Ingrid Svobodab, Hartmut FuessbRequires cookie*
 Title    Isolated versus Condensed Anion Structure VII: X-ray Structure Analysis of 1,3-Propanediammonium Dibromodichlorocadmate(II), [H3N(CH2)3NH3]CdBr2Cl2, and Estimation of Stability of Five-coordinated Halide Anions, MXg3-(M = Cd, Zn; X = Cl, Br) by Means of Ab-initio MO Calculations  
 Abstract    The coordination capability of Cl and Br in halogenocadmate(II) complexes is estimated by a solution of the structure of 1,3-propanediammonium dibromodichlorocadmate(II). The compound crystallizes as a layered anion structure with Cl bridges and Br terminals at 293 K: Imma, a = 741.56(7), b = 1869.5(5), and c -771.55(8) pm, Z = 4. In order to explain the stronger tendency of halogenocadmate(II) complexes to form layered structures as compared to halogenozincate(II), ab-initio calculations were performed. The stability of MX53-(M = Cd, Zn; X = Cl, Br) is compared. Isolated ZnX53-and CdBr53-ions are not stable. On the other hand a trigonal bipyramid CdCl53-ion is considered to be subtly stable in the crystal mainly due to Coulomb attractive interactions between the positively charged metal cation Cd2+ in a CdCl3 " fragment and two Cl-ions. 
  Reference    Z. Naturforsch. 56a, 641—646 (2001); received June 16 2001 
  Published    2001 
  Keywords    Crystal Structure, Halogenocadmate(II), Ab-initio MO Calculations 
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 TEI-XML for    default:Reihe_A/56/ZNA-2001-56a-0641.pdf 
 Identifier    ZNA-2001-56a-0641 
 Volume    56 
270Author    Requires cookie*
 Title    Zur Kenntnis der Erdalkaliantimonide und -wismutide Sr2Bi, Ba2Sb, Sr5Bi3, Ba5Sb3 und Ba5Bi3  
 Abstract    On the Earth-Alkali-A ntim onides and Bismutides Sr2Bi, B a2Sb, Sr5Bi3, B a5Sb3 and B a5Bi3 B r i g i t t e E i s e n m a n n und K l a u s D e l l e r The new compounds Sr2Bi, B a2Sb, Sr5B i3, B a5Sb3 and Ba5B i3 were prepared and their structures determined. The A 2B-compounds crystallize tetragonal bodycentered and are isotypic to Ca2Sb, Ca2Bi and Sr2Sb. The A5B 3-compounds build up the Mn5Si3-structure type. In both structures the element (V) atoms are coordinated only to earth alkali atoms. 
  Reference    (Z. Naturforsch. 30b, 66—72 [1975]; eingegangen am 23. September 1974) 
  Published    1975 
  Keywords    Earth Alkali Antimonides, Earth Alkali Bismutides, Crystal Structure 
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 TEI-XML for    default:Reihe_B/30/ZNB-1975-30b-0066.pdf 
 Identifier    ZNB-1975-30b-0066 
 Volume    30 
271Author    W. Haase, R. Mergehenn, W. KrellRequires cookie*
 Title    Die Kristallstruktur von Thiocyanato(2-dimethylaminoäthanolato)kupfer(II) The Crystal Structure of Thiocyanato(2-dimethylaminoethanalato)copper(II)  
 Abstract    The crystal structure of the title compound has been determined from three-dimensional X-ray diffractometer data. Crystals are monoclinic, space group P2i/c with 8 CU(C4HIONO)SCN units in a cell of dimensions a = 11.951(4), b = 8.954(3), c = 16.805(6) Ä, and ß = 107.5(1)°. The structure was refined by least squares techniques to a final discrepancy factor of 0.041 based on 2234 observed independent reflexions. The compound is polymeric with copper atoms alternately bridged by two oxygen atoms and two thiocyanato groups. The coordination geometry around each copper atom is distorted square pyramidal. The basal plane consists of the two bridging oxygen atoms (mean value Cu-O: 1.914(3) A), the amino nitrogen atom (mean value Cu—N: 2.035(3) A) and the nitrogen atom from the thiocyanato group (mean value Cu-N: 1.908(3) A) while the axial coordination site is occupied by a sulfur atom from a thiocyanato group (mean value Cu-S: 2.979(2) A) centrosymmetric to the first. The magnetic susceptibility of the compound shows a broad maximum at 200 K. 
  Reference    (Z. Naturforsch. 31b, 85—89 [1976]; eingegangen am 25. September 1975) 
  Published    1976 
  Keywords    Crystal Structure, Copper Compound, Thiocyanato Bridging, Spin Coupling 
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 TEI-XML for    default:Reihe_B/31/ZNB-1976-31b-0085.pdf 
 Identifier    ZNB-1976-31b-0085 
 Volume    31 
272Author    Klaus-Jürgen Range, Richard LeebRequires cookie*
 Title    Preparation and Crystal Structure of the High Pressure Phase Tm 2 S3-II  
 Abstract    Single crystals of the quenchable high pressure phase Trri2S3-II were grown from a TmJ3-flux at 10 kbar, 1600 °C. The crystals are monoclinic, space group P2i/m, with a = 11.110(5) A, 6 = 3.874(3) A, c = 10.872(5) A, ß = 108.88(2) ° and Z = 4. In Tm2S3-II, which is isotypic with Er3ScS6, the four independent thulium atoms are coordinated by six (2 x), seven and eight sulfur atoms. 
  Reference    (Z. Naturforsch. 31b, 311—314 [1976]; eingegangen am 7. November 1975) 
  Published    1976 
  Keywords    Thulium Sesquisulfide, High Pressure Phase, Crystal Structure 
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 TEI-XML for    default:Reihe_B/31/ZNB-1976-31b-0311.pdf 
 Identifier    ZNB-1976-31b-0311 
 Volume    31 
273Author    Bernd Grande, Hanskarl Müller-BuschbaumRequires cookie*
 Title    Über Oxocuprate, XIV Zur Kristallchemie von Sr2Cu304Cl2 On Oxocuprate, XIV On the Crystal Chemistry of Sr2Cu304Cl2  
 Abstract    The new compound Sr2Cu304Cl2 was prepared in melts of SrCl2. A single crystal X-ray examination (a = 546.2, c= 1259.1 pm, space group D^-14/mmm) shows that the octahedral distortion of the [Cu304Cl2] 4 ~-network cannot be explained only by the JAHN-TELLER effect. 
  Reference    (Z. Naturforsch. 31b, 405—407 [1976]; eingegangen am 24. November 1975) 
  Published    1976 
  Keywords    Strontium, Copper, Oxide Chloride, Crystal Structure, Coordination 
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 TEI-XML for    default:Reihe_B/31/ZNB-1976-31b-0405.pdf 
 Identifier    ZNB-1976-31b-0405 
 Volume    31 
274Author    K. Diehl, D. Khodadadeh, J. Kummer, SträhleRequires cookie*
 Abstract    Upon use of a synthetic method reported earlier by us respective alloys of Na/Sn, Na/Ge and Na/Sb are dissolved in ethylene-diamine and the title compounds precipitated from the solutions in high yield. By recrystal-lisation well shaped, stable crystals are obtain-ed. The crystal structure of [Na4 • 7 en]Sn9 confirms the presence of a Sn9 4 ~-polyhedron which had been suggested by us on the basis of other investigations. The Sn9 4_ -polyhedron may be described as a distorted tricapped trigonal prism. Ethylenediamine is coordi-nated to Na+-ions exclusively. 
  Reference    (Z. Naturforsch. 31b, 522—524 [1976]; eingegangen am 16. Februar 1976) 
  Published    1976 
  Keywords    Polyanionic Compounds, Germanium, Tin, Antimony, Crystal Structure 
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 TEI-XML for    default:Reihe_B/31/ZNB-1976-31b-0522_n.pdf 
 Identifier    ZNB-1976-31b-0522_n 
 Volume    31 
275Author    Heinz-Joachim HübnerRequires cookie*
 Abstract    Manganese MnGa2Se4 and MnGa2Te4 were prepared by direct synthesis from the elements at 900-1000 °C. MnGa2Se4 (Space group l!, a = 5.676(2) A, c = 10.760(3) A, z = 2) is iso-typic with CdGa2S4. 
  Reference    (Z. Naturforsch. 31b, 886—887 [1976]; eingegangen am 12. März 1976) 
  Published    1976 
  Keywords    Gallium Selenide, Manganese Gallium Telluride, Synthesis, Crystal Structure 
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 TEI-XML for    default:Reihe_B/31/ZNB-1976-31b-0886_n.pdf 
 Identifier    ZNB-1976-31b-0886_n 
 Volume    31 
276Author    R. Kipka, Hk Müller-BuschbaumRequires cookie*
 Title    Über Oxocuprate, XVI Ba9Cu7015Cl2 mit Cu 2+ in neuer Koordination About Oxocuprates, XVI Ba9Cu7015Cl2 with Cu 2+ in a New Coordination  
 Abstract    Single crystals of BagC^OisC^ were prepared and investigated by X-ray diffraction methods. They crystallize with hexagonal symmetry (a =1125.7; c = 585.3 pm, Space group D|h-P6/mmm). Cu 2 + has the well-known square 0 2--coordination. The squares are connected to rings of 6-fold symmetry. Another Cu 2+ has a so for unknown coordination of 12 0 2 ~-neighbours. The differences in respect of other oxohalogenocuprates are discussed. 
  Reference    (Z. Naturforsch. 31b, 1067—1069 [1976]; eingegangen am 24. März 1976) 
  Published    1976 
  Keywords    Barium, Copper Oxide Chloride, Crystal Structure 
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 TEI-XML for    default:Reihe_B/31/ZNB-1976-31b-1067.pdf 
 Identifier    ZNB-1976-31b-1067 
 Volume    31 
277Author    Jürgen Weis, Herbert Schäfer, Günter SchönRequires cookie*
 Title    Neue ternäre Telluride und Selenide der Alkalimetalle mit Elementen der 3. Hauptgruppe New Ternary Element(I)/Element(III)-Tellurides and Selenides  
 Abstract    The new ternary compounds NaAlSe2, NaAlTe2, NaGaTe2 and KAlTe2 crystallize in the Tl I Tl III Se2-structure type. The analogous Tl-compounds build up the same structure but show a variable composition within the limits (NaJTli_a.)TlSe2 (Oca; <0.47) and (Ka.Tli_jr)TlSe2 (0 <x <0.56). The compounds KAlSe2, KGaSe2, KInSe2 and KGaTe2 crystallize in a new structure type. 
  Reference    (Z. Naturforsch. 31b, 1336—1340 [1976]; eingegangen am 5. Juli 1976) 
  Published    1976 
  Keywords    Ternary Tellurides, Ternary Selenides, Crystal Structure 
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 TEI-XML for    default:Reihe_B/31/ZNB-1976-31b-1336.pdf 
 Identifier    ZNB-1976-31b-1336 
 Volume    31 
278Author    Brigitte Eisenmann, Gerhard Savelsberg, Herbert SchäferRequires cookie*
 Title    Zur Darstellung und Kristallstruktur von Na2CuAs, K2CuAs und K2CuSb Preparation and Crystal Structure of Na2CuAs, K2CuAs and K2CuSb  
 Abstract    The three new compounds crystallize orthorhombic, space group Cmcm with Na2CuAs: a = 8.86(2) A, b = 7.22(2) A, c = 5.34(2) A; K2CuAs: a = 10.02(2) A, b = 7.56(2) A, c = 5.89(2) A; KsCuSb: a = 10.50(2) A, b = 7.93(2) A, c = 6.23(2) A. There are Cu-E(V)-Cu-E(V)-zigzag-chains in the structure, in which the Cu-atoms are linearly bonded to the E(V)-atoms. 
  Reference    (Z. Naturforsch. 31b, 1344—1346 [1976]; eingegangen am 15. Juli 1976) 
  Published    1976 
  Keywords    Intermetallic Compounds, Crystal Structure, Ternary Arsenides, Ternary Antimonides 
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 TEI-XML for    default:Reihe_B/31/ZNB-1976-31b-1344.pdf 
 Identifier    ZNB-1976-31b-1344 
 Volume    31 
279Author    Helmut Rieskamp, Rainer MattesRequires cookie*
 Title    Fluorreiche Oxofluorovanadate(V): Die Kristallstruktur von [enH2] [VOF5]  
 Abstract    The crystal structure of triclinic [enH2][VOF5], prepared in aqueous solution, has been determined from X-ray diffractometer data (i? = 0.076 for 527 reflections). The structure contains monomeric [VOFs] 2--ions. The bond distances are 1.54(1) Ä (terminal oxygen), 1.80(1) (average for the cis-fluorine atoms) and 2.10(1) Ä for the fluorine atom in trans-position to the terminal oxygen atom. This fluorine atom is involved in strong hydrogen bonds originating from the [NHaCH^CH^NEy 2 " 1 -cation with cisoid conformation. Earlier results about the existence of K2VOF5 could not be confirmed. 
  Reference    (Z. Naturforsch. 31b, 1453—1455 [1976]; eingegangen am 2. August 1976) 
  Published    1976 
  Keywords    Oxopentafluorovanadates(V), Crystal Structure, Vibrational Spectra 
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 TEI-XML for    default:Reihe_B/31/ZNB-1976-31b-1453.pdf 
 Identifier    ZNB-1976-31b-1453 
 Volume    31 
280Author    Gerhard Cordier, Herbert SchäferRequires cookie*
 Title    Neue intermetallische Verbindungen im arcJi-Ce202S-Strukturtyp New Intermetallic Compounds in the awfa"-Ce202S-Structure Type  
 Abstract    The new intermetallic compounds CaMn2Sb2, SrMn2Sb2 and CaMn2Bi2 have been prepared and structurally characterized. They are isotypic and crystallize trigonal in the an^-Ce202S-structure with the lattice constants: CaMn2Sb2: a = 4.54(1), c = 7.48(1), c/a = 1.65. SrMn2Sb2: a = 4.56(1), c = 7.70(1), c/a = 1.69. CaMn2Bi2: a = 4.63(1), c = 7.64(1), c/a = 1.65. 
  Reference    (Z. Naturforsch. 31b, 1459—1461 [1976]; eingegangen am 13. August 1976) 
  Published    1976 
  Keywords    Intermetallic Compounds, Crystal Structure, Ternary Antimonides, Ternary Bismutides 
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 TEI-XML for    default:Reihe_B/31/ZNB-1976-31b-1459.pdf 
 Identifier    ZNB-1976-31b-1459 
 Volume    31