Das Schwingungsspektrum von Sr2V2O7 und die Schwingungseigenschaften des Divanadat-Ions

The infrared and laser-Raman spectra of Sr₂V₂O₇ are reported and discussed by means of a Site Symmetry analysis. The principal force constants as well as the mean amplitudes of vibration for the V₂O₇ ^4– ion have been calculated using a simplified molecular model. Some aspects of the vibrational behaviour of the V–O–V bridge in this ion are also discussed.

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22. Mitt. der Reihe Orthovanadate und verwandte Verbindungen. 21. Mitt.:M. E. Escobar undE. J. Baran, Z. Naturforsch.B32, 349 (1977); 20. Mitt.:E. J. Baran undI. L. Botto, Mh. Chem.,108, 311 (1977); 19. Mitt.:E. J. Baran, Z. anorg. allgem. Chem.427, 131 (1976).     

Das Schwingungsspektrum von Barium-Divanadat

The infrared and laser-Raman spectra of crystalline Ba₂V₂O₇ are reported and discussed by means of a Site Symmetry analysis.

28. Mitt. der Reihe Orthovanadate und verwandte Verbindungen. 27. Mitt.:E. J. Baran undM. E. Escobar, J. Phys. Chem. Solids, im Druck; 26. Mitt.:E. J. Baran, I. L. Botto, J. F. Ramos undP. J. Aymonino, Mh. Chem.109, 1139 (1978); 25. Mitt.:E. J. Baran, J. Mol. Struct.48, 441 (1978); 24. Mitt.:E. J. Baran undI. L. Botto, J. inorg. nucl. Chem.40, 1603, (1978); 23. Mitt.:M. E. Escobar undE. J. Baran, Z. Anorg. allg. Chem.,441, 273 (1978).     

Das Schwingungsspektrum von Magnesium-orthovanadat

The infrared and laser-Raman spectra of crystalline Mg₃(VO₄)₂ are reported and a factor group analysis for the full lattice is presented to support the discussion. The 1,000 to 600 cm^?1 region of the spectrum is essentially related to internal (stretching) modes of the greatly distorted VO₄ tetrahedra, whereas the bands in the low frequency region must be assigned to complex vibrations originating in the interaction of the bending vibrations of the tetrahedral groups with the external modes.     

Das Schwingungsspektrum von Ba2ZnTeO6

The Vibrational Spectrum of Ba₂ZnTeO₆ The vibration modes of Ba₂ZnTeO₆ are assigned to TeO₆ octahedra linked by apexes and sharing faces respectively. Both octahedra types show different force constants, bond order, and Te? O distances.     

Das Schwingungsspektrum von kristallinem syndiotaktischem Polyvinylchlorid

Ohne Zusammenfassung     

Das Schwingungsspektrum von Li5ReO6

The infrared and laser-Raman spectra of crystalline Li₅ReO₆ are reported and discussed and some comparisons with other lithium hexaoxometallates are made.     

Das Schwingungsspektrum von Ba5(ReO6)2

The infrared and laser-Raman spectra of crystalline Ba₅(ReO₆)₂ are reported and discussed. From the obtained spectroscopic data a calculation of force constants and mean amplitudes of vibration for the ReO₆ ^5– ion has been carried out.

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Das Schwingungsspektrum des Trimethyl-s-triazins

The Vibrational Spectra of Trimethyl-s-triazine The vibrational spectra (IR and Raman) of trimethyl-s-triazine have been measured, discussed and assigned. For the (dissolved) compound the data point to a planar six membered ring of (pseudo-)D_3h symmetry.     

Das Schwingungsspektrum des synthetischen Carnotits

The infrared and laser-Raman spectra of synthetic carnotite, K₂[(UO₂)₂V₂O₈], are reported and discussed. Force constants for the terminal V-O bonds as well as for the UO₂ ²⁺ ions are evaluated. From the spectroscopic data, a U-O bond length of 1.81 Å is estimated for the uranyl ion in this compound.

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15. Mitteilung der Reihe Orthovanadate und verwandte Verbindungen 14. Mitt:E. J. Baran, J. C. Pedregosa undP. J. Aymonino, Mh. Chem.106 1085 (1975).     

Das Schwingungsspektrum von α-Te2MoO7 und ein Vorschlag zur Struktur der Telluromolybdate zweiwertiger Kationen

Vibrational Spectrum of α-Te₂MoO₇ and a Proposal for the Structure of Telluromolybdates of Divalent Cations Infrared and Raman spectra of α-Te₂MoO₇ have been recorded and discussed in relation to their known crystalline structure. The comparison of these spectra with those of telluromolybdates of the type M^IITeMoO₆, allows us to propose a structural model for these phases, which is totally consistent with the spectroscopic findings.     

Synthese und Kristallstruktur von Pb2P4O12 · 3 H2O

Synthesis and Crystal Structure Determination of Pb₂P₄O₁₂ · 3 H₂O Pb₂P₄O₁₂ · 3 H₂O precipitates at mixing aqueous solutions of Pb(NO₃)₂ and Na₄P₄O₁₂ (25°C). Crystal growth was achieved by applying gel-techniques (Agar-Agar-gel). The crystal structure (P1 , a = 786.4(3), b = 914.4(3), c = 1021.6(3) pm, α = 97.42(2)°, β = 100.63(2)°, γ = 114.92(2)°; Z = 2; 4160 unique diffractometer data, R = 0.05) contains cyclo-tetraphosphate anions with point symmetry D_2d. Lead is coordinated by eight oxygen, the polyhedra deriving from a square antiprism.     

Über gemischtvalente Oxoplumbate. Zur Kenntnis von Rb2Pb4O7 = Rb2PbPbO7

On Mixed-valent Oxoplumbates. On Rb₂Pb₄O₇ = Rb₂Pb Pb O₇ For the first time, Rb₂Pb₄O₇ has been prepared by annealing mixtures of Rb₂O₃ and PbO with Rb:Pb = 1:2 [Ag-cylinders, sealed under vacuum in Duran-glass ampoule, 450°C, 30 d (single crystals)]. The rubin red single crystals are of longish [001] shape. The structure determination [5162 symmetry independent hkl, four-circle-diffractometer CAD 4 (Fa. Enraf-Nonius), ω-2Θ—scan, AgKα, ψ-scan absorption correction, R = 7.54%, R_W = 7.71%] confirms the space group P1 with a = 1036.00(10), b = 733.72(8), c = 663.54(10) pm, α = 90.049(12)°, β = 99.236(12)°, γ = 101.641(12)°, Z = 2, d_rö = 7,58 g · cm^?3, d_pyk = 7,55 g · cm^?3. The structure is characterized by a layer-lattice. The coordination number is three for Pb²⁺, six for Pb⁴⁺. The Madelung Part of Lattice Energy, MAPLE, Effective Coordination Numbers, ECoN, these via Mean Effective Ionic Radii, MEFIR, are calculated.     

Elektrochemische Synthese von Ag5Pb2O6

Electrochemical Synthesis of Ag₅Pb₂O₆ Ag₅Pb₂O₆ was prepared by anodic oxidation of silver in a PbO₂ suspension in an aqueous KOH solution. Phase purity was checked by a Rietveld‐fit of the X‐ray powder pattern, thermal and chemical analysis. The compound exhibits ionic conductivity. It' anisotropy leads to an orientation of the crystallites on the silver anode.     

Oriented Formation of Pb2P2O7 from K2Pb[P4O12]

Cyclotetraphosphate K₂Pb[P₄O₁₂] transforms into the lead diphosphate Pb₂P₂O₇ crystallographically oriented by heating up to its transformation point at 537°C in a moist atmosphere. The oriented formation of diphosphate takes place by means of epitaxy.     

Das Schwingungsspektrum des Ti[N(CH3)2]4

Zusammenfassung Die Infrarot- und Ramanspektren von Ti[N(CH₃)₂]₄ werden mitgeteilt, zugeordnet und mit den Spektren der analogen Dimethylamino-Verbindungen von Si, Ge und Sn verglichen.

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The IR and Raman spectra of Ti[N(CH₃)₂]₄ are reported, assigned and compared with those of the Si, Ge and Sn analoga.

     

Mg2Na2V10O28·20H2O and Mg3V10O28·28H2O

The crystal structures of dimagnesium disodium decavanadate icosahydrate, Mg₂Na₂V₁₀O₂₈·20H₂O, (I), and trimagnesium decavanadate octacosahydrate, Mg₃V₁₀O₂₈·28H₂O, (II), have been determined by single‐crystal X‐ray diffraction. They crystallize with monoclinic (C2/c) and triclinic () symmetry, respectively. All the Mg²⁺ cations in (I) and (II) are octahedrally coordinated by six water mol­ecules. The Na⁺ cations in (I) are coordinated by three water mol­ecules and three O atoms of the decavanadate anions, and link the latter into a three‐dimensional network. The decavanadate anions in (II) are not linked to one another.