Go toArchive
Browse byFacets
Bookbag ( 0 )
Facet   section ZfN Section B:Volume 035  [X]
Results  345 Items
Sorted by   
Publication Year
1980 (345)
121Author    Peter Paetzold, Günther SchimmelRequires cookie*
 Title    ungesättigter Stickstoffbasen Boration Reactions with the N-Oxides and m-Imines of Unsaturated Nitrogen Bases  
 Abstract    -Dipolar reagents with an unsaturated CNO-or CNN-skeleton undergo 1,3-organo-boration by triorganoboranes. On the other hand, the unsaturated NNO-skeletons in azoxybenzene or nitrous-oxide are reduced to the corresponding NN-fragment by trialkyl-boranes. The 1,3-addition of aminoborane Cl2BNMe2 to the aldimineoxide PhHC = NMe-0 represents one of the rare examples of analogous reactivity of BN-and CC-double bonds. O-Borylhydroxylamines PhHCR-NMe-OBR2 are reduced by BR'3 to PhHCR-NMe-BR'2 and R'0-BR2. Similar reduction products are isolated from liquid-phase thermolysis of PhHCEt-NMe-OBEt2 (16), whereas gas-phase thermolysis of 16 gives PhCH = NMe, (EtBO)3, and C4HI0. 
  Reference    Z. Naturforsch. 35b, 568—577 (1980); eingegangen am 6. Dezember 1979 
  Published    1980 
  Keywords    O-Borylhydroxylamines, Borylhydrazines, 2-Borylhydrazones, Organoboration, Aminoboration 1, 3 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-0568.pdf 
 Identifier    ZNB-1980-35b-0568 
 Volume    35 
122Author    Horst Richter, Ekkehard Fluck, Wolfgang SchwarzRequires cookie*
 Title    Reaktion von Imidodiphosphorsäuretetraphenylester mit Quecksilber(II)-oxid und Phenylquecksilberhydroxid Reaction of Imidodiphosphoric Tetraphenylester with Mercury (II) Oxide and Phenylmercuryhydroxide  
 Abstract    Imidodiphosphoric Tetraphenylester, Diazadiphosphadimercuracyclododecin Reaction of imidodiphosphoric tetraphenylester with HgO yields the twelve-membered ring system 1, the properties, NMR and X-ray structural data of which are reported. A reaction mechanism is suggested. Reaction product from imidodiphosphoric tetraphenyl-ester and CöHöHgOH is N-phenylmercury-bis(phosphoric diphenylester)-imide (2). 
  Reference    Z. Naturforsch. 35b, 578—583 (1980); eingegangen am 3. Dezember 1979 
  Published    1980 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-0578.pdf 
 Identifier    ZNB-1980-35b-0578 
 Volume    35 
123Author    H. Schmidbaur, G. BlaschkeRequires cookie*
 Title    Ein Ylidkomplex des Rutheniums mit drei-und viergliedrigen Metallocyclen An Ylide Complex of Ruthenium with Three-and Four-Membered Metallocycles  
 Abstract    A spirometallocyclic complex of ruthenium with (CH3)2P(CH2)2, (CH3)2PCH2 and two (CH3)3P ligands (formula 5) is synthesized from (CH3)2P(CH2)2Li and frans-[(CH3)3P]4RuCl2 in the molar ratio 2:1. Two equivalents of (CHs^P are liberated and the ionic complex frans-[(CH3)3P]4Ru[CH2P(CH3)3]Cl + Cl _ is formed as a by-product. The products were characterized by analytical and spectroscopic data. 
  Reference    Z. Naturforsch. 35b, 584—587 (1980); eingegangen am 11. November 1979 
  Published    1980 
  Keywords    Ylide Complexes, Ruthenium, Metallocycle 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-0584.pdf 
 Identifier    ZNB-1980-35b-0584 
 Volume    35 
124Author    GerhardN. Schrauzer, Masao Hashimoto, Abdussalam MaihubRequires cookie*
 Title    Studies on Vitamin B12 and Related Compounds, 50 Synthesis of Substituted Alkylcobalamins from Vitamin B12r and Radicals Generated from Aldehydes, Alcohols and Ethers under "Oxidizing-Reducing" Conditions. A New Synthesis of Coenzyme B12 [1]  
  Reference    Z. Naturforsch. 35b, 588 (1980) 
  Published    1980 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-0588.pdf 
 Identifier    ZNB-1980-35b-0588 
 Volume    35 
125Author    Herbert Schumann, Manfred MeissnerRequires cookie*
 Title    Organometallphosphin-substituierte Übergangsmetallkomplexe, XXVI [1] Diearbonyl-nitrosyl-organometaUphosphin-kobalt-Komplexe Organometalphosphine-Substituted Transition Metal Complexes, XXVI [1] Dicarbonyl Nitrosjd Organometal Phosphine Cobalt Complexes  
 Abstract    The reactions of tricarbonyl nitrosyl cobalt with tri-feri-butylphosphine, di(teri-butyl)-trimethylsilyl-, -germyl-, -stannylphosphine, £er£-butyl-bis(trimethylsilyl)-, -(germyl)-, -(stannyl)phosphine, as well as with tris(trimethylsilyl)-, -(germyl)-, and -(stannyl-phosphine result in the elimination of one CO-ligand and the formation of corresponding dicarbonyl-nitrosyl-organometal phosphine cobalt complexes. The NMR spectra of the products are reported and discussed. 
  Reference    Z. Naturforsch. 35b, 594—598 (1980); eingegangen am 5. Dezember 1979 
  Published    1980 
  Keywords    Organometal Phosphines, Dicarbonyl-nitrosyl Cobalt Complexes, NMR Spectra 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-0594.pdf 
 Identifier    ZNB-1980-35b-0594 
 Volume    35 
126Author    Nils Wiberg, Heinz-Wolfgang Häring, Ulrich SchubertRequires cookie*
 Title    Darstellung und Eigenschaften des Nitrenkomplexes (C5H5)2VNSiMe3 Zur Reaktion von Vanadocen mit Silylaziden [1] Reaction of Vanadocene with Silyl Azides Preparation and Properties of the Nitrene Complex (CsHs^VNSiMes [1]  
 Abstract    Trimethy lsily lnitrene -bis (n-cyclopentadienyl) vanadium, Bis(trimethylsilylnitrene)-bis(^-cyclopentadienyl)divanadiumdichloride, Tris(^-trimethylsilylnitrene)-bis(rc-cyclopentadienyl)divanadium 
  Reference    Z. Naturforsch. 35b, 599—603 (1980); eingegangen am 11. Dezember 1979 
  Published    1980 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-0599.pdf 
 Identifier    ZNB-1980-35b-0599 
 Volume    35 
127Author    Eine Neutronenbeugungsuntersuchung, M. Wintenberger, F. Tcheou, J. David, J. LangRequires cookie*
 Title    Verfeinerung der Struktur des Nitrids MgSiN2 - A Refinement of the Structure of the Nitride MgSiN2 -a Study by Neutron Diffraction  
 Abstract    The tetrahedral wurtzite type structure of MgSiN2 has been refined with the help of neutron diffraction. The interatomic distances for Mg-N and Si-N are in complete agreement with the previously known values and the SiN4 tetrahedra in the structure are slightly deformed. 
  Reference    Z. Naturforsch. 35b, 604—606 (1980); eingegangen am 27. Dezember 1979 
  Published    1980 
  Keywords    Nitride, Tetrahedral Structure, Neutron Diffraction 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-0604.pdf 
 Identifier    ZNB-1980-35b-0604 
 Volume    35 
128Author    JohannesC P M Lapidaire, WillemL. GroeneveldRequires cookie*
 Title    Dodecamethyl Bisimidotriphosphoramide (TRIPA) A Tridentate Ligand, Part II [1]  
 Abstract    In this article we describe the synthesis of TRIPA, dodecamethyl bisimidotriphosphor-amide (C12H36N7O3P3) and of its complexes with various lanthanide-nitrates. Five types of complexes have been isolated according to the compositions, X-ray diffraction patterns and IR spectra. 1. M(N03)3(TRIPA)3(acetone) M = La, Pr, Nd, 2. M(N03)3(TRIPA) M = Y, 3. M(N03)3(TRIPA)2(nitromethane) M = Er, Y, 4. M(N03)3(TRIPA)2(acetone) M = Sm, Gd, Dy, Er, Y (type I), 5. M(N03)3(TRIPA)2(acetone) M = Y (type II). The yttrium complexes, type I and II, are isomeric. IR spectra are given together with the NMR spectra. It is concluded that in all complexes the three TRIPA oxygens are coordinated, except in group 1. The nitrate groups in group 2 to 5 are involved in the coordination, particularly in the type 2 complex, where there are bidentate nitrate groups. There seems to be a difference in the conformation of the TRIPA molecules between the free ligand, the complexes in group 1, in group 2 and in group 3, 4, 5 Hygroscopic TRIPA can be easily confused with a stable mono-hydrate, TRIPA • H20. 
  Reference    Z. Naturforsch. 35b, 607—613 (1980); received October 15 1979/January 9 1980 
  Published    1980 
  Keywords    Complex Formation, Lanthanide-nitrates, Tridentate ligand, Phosphoryl Compound, TRIPA 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-0607.pdf 
 Identifier    ZNB-1980-35b-0607 
 Volume    35 
129Author    Hans-Friedrich Klein, Joachim Groß, Jean-Marie Bassett, Ulrich SchubertRequires cookie*
 Title    Semicobaltate -Alkalimetall-Träger in Kohlenwasserstoffen Darstellung, Eigenschaften und Struktur von K[Co(C2H4)(PMe3)3]2 Semicobaltates -Alkali Metal Carriers in Hydrocarbons Synthesis, Properties, and Structure of K[Co(C2H4)(PMe3)3]2  
 Abstract    Semicobaltates (Co-1/2) containing olefin and trimethylphosphane ligands are synthe-sized from Co(olefin)(PMe3)3 and potassium metal. The X-ray crystal structure determina-tion of the title compound shows that the unit cell contains two K atoms in equal ionic contact with the ethylene ligands of four Co(C2H4)(PMe3)3 complex units, two of which are interacting with both K atoms. In solution the semicobaltates exist in hydrocarbon solvents under argon only, while in contrast under ethylene or nitrogen atmospheres or in donor solvents disproportionation occurs to give Co(O) and Co(-I) species. Allgemeines 
  Reference    Z. Naturforsch. 35b, 614—619 (1980); eingegangen am 3. Januar 1980 
  Published    1980 
  Keywords    Potassium-Ethylene Semicobaltate, Synthesis, Molecular Structure, Crystal Structure 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-0614.pdf 
 Identifier    ZNB-1980-35b-0614 
 Volume    35 
130Author    Albrecht MewisRequires cookie*
 Title    Neue ternäre Phosphor-und Arsenverbindungen mit Zr2Fe12P7-Struktur New Ternary Compounds of Phosphorus and Arsenic with the Zr2Fei2P7-Structure  
 Abstract    The ternary compounds Mg2.5Ni11.5P7, Ca2.1Ni11.9P7 and Ca2.3Nin.7As7 were structurally characterized. They are isotypic and crystallize in the Zr2Fei2P7-type (space group P 6) with the following constants: 
  Reference    Z. Naturforsch. 35b, 620—625 (1980); eingegangen am 11. Januar 1980 
  Published    1980 
  Keywords    Phosphides, Arsenide, 2 A Elements, Nickel, Crystal Structure 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-0620.pdf 
 Identifier    ZNB-1980-35b-0620 
 Volume    35 
131Author    Karl Berroth, Hansjürgen Mattausch, Arndt SimonRequires cookie*
 Title    Neue reduzierte Halogenide der Lanthanoide mit kondensierten Clustern: Tb6Br7 und Er6I7 New Reduced Halides of Rare Earth Metals with Condensed Clusters: TböBr? and Er6l7  
 Abstract    The new compounds TböBr? and Er6l7 are formed from the trihalides with an excess of metal in sealed tantalum containers. X-ray structure investigations [space group C2/m; Tb6Br7 (Er6I7): a = 2057.1 (2137.5), b = 379.3 (386.9), c = 1180.0 (1231.9) pm, ß = 124.59° (123.50°)] show one-dimensional regions connected by Ln-Ln bonds. The structure type can be described in terms of LnöXi2-clusters which are linked via edges of Ln6-octahedra to form double strings. The structure is derived from an FCC arrangement of halogen atoms part of which is systematically substituted by Ln6-octahedra. 
  Reference    Z. Naturforsch. 35b, 626—630 (1980); eingegangen am 10. Januar 1980 
  Published    1980 
  Keywords    Condensed Clusters, Reduced Rare Earth Halides, Crystal Structure 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-0626.pdf 
 Identifier    ZNB-1980-35b-0626 
 Volume    35 
132Author    Fritz Seel, Rudi Lehnert, Eckhard Bill, Alfred TrautweinRequires cookie*
 Title    Produkte der Umsetzung des Pentacarbonyleisens mit N-substituierten Imidazolen Products of the Reaction of Pentacarbonyl Iron with N-Substituted Imidazoles  
 Abstract    1-Methyl-, 1-ethyl-, 1,2-dimethyl-and 1,2,3,4-tetramethylimidazole react with penta-carbonyliron to yield [FeIm6][Fe(CO)8] (1), [FeIm6][Fe(CO)4]2 (2), [FeIm4][Fe(CO)4] (3) and Fe(Im)(CO)2 (4) (Im = substituted imidazole). The crystal and molecular structures of 1 and 2 have been determined by X-ray diffraction. For 1 and 2 agreement between calculated and measured Mössbauer absorption intensities was obtained by taking into account Debye-Waller-factors, which were derived from the X-ray diffraction experiments. 
  Reference    Z. Naturforsch. 35b, 631—638 (1980); eingegangen am 18. Dezember 1979 
  Published    1980 
  Keywords    Imidazole Derivatives, Pentacarbonyl Iron, Crystal Structure, Molecular Structure, Mößbauer Spectra 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-0631.pdf 
 Identifier    ZNB-1980-35b-0631 
 Volume    35 
133Author    Herbert Schumann, Manfred Meißner, Heinz-Jürgen KrothRequires cookie*
 Title    NMR-Untersuchungen an Organoelement(IVb)-phosphinen, VI [1] 61 Ni-NMR-Untersuchungen an Organoelement(rVb)-phosphin-8ubstituierten Komplexen des Tetracarbonylnickel NMR Studies on Organoelement(IVb)-phosphines, VI [1] 61 Ni NMR Spectroscopic Investigations on Organoelement(IVb) Substituted Complexes of Tetracarbonylnickel  
  Reference    Z. Naturforsch. 35b, 639—641 (1980); eingegangen am 7. Januar 1980 
  Published    1980 
  Keywords    Phosphine Substituted Carbonyl Nickel Complexes, 61 Ni NMR Organometal Phosphines, Tricarbonyl Nickel Complexes, 61 Ni NMR 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-0639.pdf 
 Identifier    ZNB-1980-35b-0639 
 Volume    35 
134Author    KlausG. Heumann, Klaus Baier, Gerald WibmerRequires cookie*
 Title    Chlor-Isotopenseparation an einem wasserhaltigen Zirkondioxidaustauscher Chlorine Isotope Separation Using an Hydrous Zirconium Dioxide Exchanger  
 Abstract    zirconium dioxide is used in column experiments for separating the halide ions as well as for isotope fractionation of chlorine. The preparation of the zirconium dioxide particles is carried out by homogeneous hydrolysis of a zirconyl chloride solution using hexamethylenetetramine. The separation order of the halides is I -, Br -and Cl -in contrast to the inverse separation order using a strongly basic anion exchange resin. In chlorine isotope separation experiments an enrichment of 35 C1~ is found in the first fractions, whereas the last fractions show a significant enrichment of 37 C1~. This also indicates an inversion of the isotope separation compared with a strongly basic anion exchange resin. A dependence of the isotope fractionation on the concentration of the NaNC>3 solution used as eluant is found. With increasing concentration the isotope fractionation decreases. Using a 0.5 M NaN03 solution the elementary separation effect was calculated e = 6,1 • 10~ 4 . This is one of the highest isotope fractionations known in a chloride isotope exchange system. The results show that the electrolyte behaviour of isotopes is comparable to that of a series of homologous elements. 
  Reference    Z. Naturforsch. 35b, 642—647 (1980); eingegangen am 11. Januar 1980 
  Published    1980 
  Keywords    Isotope Separation, Chlorine, Zirconium Dioxide, Column Experiments, Halide Separation Hydrous 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-0642.pdf 
 Identifier    ZNB-1980-35b-0642 
 Volume    35 
135Author    Walter Strohmeier, Manfred Michel, Luise WeigeltRequires cookie*
 Title    mit homogenen Ir-und Ru-Katalysatoren Selective Bulk-Hydrogenation of a,ß Unsaturated Ketones to Ketones with Homogeneous Ir and Ru Catalysts  
 Abstract    a,ß Unsaturated ketones are selectively hydrogenated to ketones in homogeneous bulk-catalysis under mild conditions by iridium-and ruthenium complexes. The range of mean turnover is from 6 to 196 depending on substrate, catalyst and reaction conditions. Selectivity ketone/alcohol depends on the degree of conversion and exceeds 100 on con-version of 90%. Einleitende Bemerkungen 
  Reference    Z. Naturforsch. 35b, 648—650 (1980); eingegangen am 7. Dezember 1979 
  Published    1980 
  Keywords    Catalysis, Homogeneous, Selective, Hydrogenation, Unsaturated Ketones 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-0648.pdf 
 Identifier    ZNB-1980-35b-0648 
 Volume    35 
136Author    HansJoachim Berthold, Wolfgang LudwigRequires cookie*
 Title    Präparative und röntgenographische Untersuchungen über Cäsium-Silber-Gold(III)-Chlorid Preparation and X-ray Investigations of Cesium Silver Gold(III) Chloride  
 Abstract    Cesium silver gold(III) chloride has been prepared from hydrochloric acid solutions. The composition of the preparations is variable and depends on the ratio [Au(III)]/[Ag(I)] in solution. It corresponds to the formula Cs2Agi_aAui+a;/3Cl6. In the range 0 < x < 0,64 six crystallographically different phases have been observed. Above x — 0,42 a cubic phase is obtained. The stoichiometric compound Cs2AgAuCl6 is obtained only from solutions with [Au(III)]/[Ag(I)] < 1. Reports in the literature which claim the stoichiometric compound Cs2AgAuCl6 to exist in a cubic and in a tetragonal form cannot be confirmed. Cs2AgAuCl6 crystallizes ortho-rhombically with the lattice constants a = 15,21 A, b= 15,16 A and c= 10,32 A (Z = 8). 
  Reference    Z. Naturforsch. 35b, 651—656 (1980); eingegangen am 7. Februar 1980 
  Published    1980 
  Keywords    Cesium Silver Gold(III) Chloride, Preparation, Chemical Composition, Nonstoichiometric Phases, Lattice Constants 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-0651.pdf 
 Identifier    ZNB-1980-35b-0651 
 Volume    35 
137Author    Oskar Glemser, Eckehard Kindler, Bernt Krebs, Rüdiger Mews, Frank-Michael Schnepel, Joachim WegenerRequires cookie*
 Title    Über das Bis(chlor8chwefel)stick8loff-Kation N(SC1)2 + On the Bis(chlorosulfur)nitrogen Cation N(SC1)2 +  
 Abstract    The synthesis of N(SC1)2+ MF6~ (M = As, Sb) is reported, the structure of N(SC1)2+ AlCLr is determined and some of the spectroscopic properties of the N(SC1)2 + cation are discussed. Das Bis(chlorschwefel)Stickstoff-Kation wurde erstmals aus NSF3 und BCI3 dargestellt [1]: 
  Reference    Z. Naturforsch. 35b, 657—660 (1980); eingegangen am 15. Februar 1980 
  Published    1980 
  Keywords    Bis(chlorosulfur)nitrogen Hexafluoroarsenate, Hexafluoroantimonate, Tetrachloroaluminate, Vibrational Spectra 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-0657.pdf 
 Identifier    ZNB-1980-35b-0657 
 Volume    35 
138Author    Helmut Behrens, Jochen Ellermann, EwaldF. HohenbergerRequires cookie*
 Title    Dicarbonyl-, Carbamoyl-carbonyl-und Carbomethoxo-carbonyl-Komplexe des Rhodiums mit tri-und tetratertiären Phosphinliganden [1] Dicarbonyl-, Carbamoyl-carbonyl-and Carbomethoxo-carbonyl Complexes of Rhodium with Tri-and Tetratertiary Phosphine Ligands [1]  
 Abstract    The cationic dicarbonyl complexes [Rh(CO)2(R2PCH2)3CR']PF6 (R = C6H5; R' = CH3, -CH2PR2), formed by high pressure synthesis from RhCl3(H20)3, CO and (R2PCH2)3CR' react with liquid ammonia at 20 °C to give the carbamoyl complexes Rh(CO)(CONH2)(R2PCH2)3CR'. At 100 °C in liquid ammonia the carbamoyl-carbonyl complexes Rh(CO)(CONH2)(R2PCH2)3CR' form the CO-bridged, dinuclear compounds (^-CO)2[Rh(R2PCH2)3CR']2. Upon treatment of Rh(CO)(CONH2)(R2PCH2)3CR' with CH3OH the carbomethoxo carbonyl complexes Rh(CO)(COOCH3)(R2PCH2)3CR' are obtained. The new compounds were characterised, as far as possible, by their IR, Raman and 31 P NMR spectra. 
  Reference    Z. Naturforsch. 35b, 661—668 (1980); eingegangen am 10. Dezember 1979/30. Januar 1980 
  Published    1980 
  Keywords    Rhodium Complexes, Polytertiary Phosphines, IR Spectra, Raman Spectra, 31 P NMR Spectra 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-0661.pdf 
 Identifier    ZNB-1980-35b-0661 
 Volume    35 
139Author    D. Chales De Beaulieu, Hk Müller-BuschbaumRequires cookie*
 Title    Gemischtvalente Oxovanadate, I Ein neuer Strukturtyp für die Verbindung BaV10O15 Oxovanadates with Mixed Valence, I A New Crystal Structure of BaVioOis  
 Abstract    BaVioOis was prepared by high temperature reaction of BaO and V2O3 in H2-atmosphere (T > 1800°). X-ray investigations of single crystals show a new structure type with octa-hedral coordination of V 3+ /V 2+ (statistical distribution) and cuboctahedral surrounding of Ba 2+ . Orthorhombic symmetry, space group D^|-Ccmb, a = 995,8; b = 1161,8; c = 941,0; Z = 4. 
  Reference    Z. Naturforsch. 35b, 669—671 (1980); eingegangen am 5. Februar 1980 
  Published    1980 
  Keywords    Barium, Vanadium, Oxide, Mixed Valence State, Crystal Structure 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-0669.pdf 
 Identifier    ZNB-1980-35b-0669 
 Volume    35 
140Author    ChrL. TeskeRequires cookie*
 Title    Ba2ZnGe2S60: Ein neues Oxidsulfid mit Tetraedergerüststruktur On Ba2ZnGe2S60. A New Oxide Sulfide with Tetrahedral Framework Structure  
 Abstract    Crystal Structure, Topological Linkage of Tetrahedra Ba2ZnGe2SeO was prepared for the first time and the crystal structure determined by using single crystal X-ray methods. The space group is Dfd-P42im, tetragonal (No. 113). Lattice constants: a = 963.59 ± 0.22; c = 645.06 ± 0.25 pm. The tetrahedral framework structure is described and discussed. Zn is linked only to sulfur. The oxygen belongs to the coordination sphere of Ge and Ba. 
  Reference    Z. Naturforsch. 35b, 672—675 (1980); eingegangen am 21. Januar 1980 
  Published    1980 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-0672.pdf 
 Identifier    ZNB-1980-35b-0672 
 Volume    35 
Prev
...
6
7
8
9
10
...
Next