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  • Inorganic Chemistry  (21)
  • Biochemistry  (3)
  • Wiley-Blackwell  (24)
  • Springer
  • 1985-1989  (24)
  • 1930-1934
  • 1985  (24)
Collection
Publisher
  • Wiley-Blackwell  (24)
  • Springer
Years
  • 1985-1989  (24)
  • 1930-1934
Year
  • 1
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Syntheses and Conformational Properties of Stereoisomeric 1,3-Cyclohexanediol and 3-Aminocyclohexanol Derivatives. X-Ray Structure Analysis of trans-1,3-Dihydroxy-1,5,5-trimethylcyclohexane and c-3-Amino-r-1-hydroxy-1,5,5-trimethylcyclohexaneSolvomercuration of cyclohexenols 3 and 4 yields the respective cis/trans-diols 1a and pure trans-diol 2a. Via the monotosylates the analogous cis-diol cis-2a as well as the cis-amino alcohols cis-1b and cis-2b are prepared diastereomerically pure in good yields by SN2 reaction with KHCO3/18-crown-6 and KN3/18-crown-6, resp., followed by LiAlH4 reduction. NMR spectroscopic investigations show that in the cis-series the bisaxial (cis-1-sc-sc) or the trisaxial (cis-2-sc-sc) conformations - stabilized by an intramolecular H-bond - exist in aprotic solvents, while in protic media the inverted chair conformations (cis-1-ap-ap and cis-2-ap-ap) dominate. The conformational interactions in the higher substituted compounds 2 are investigated by X-ray structure analyses of a cis (cis-2b) and a trans (trans-2a) representative.
    Notes: Die Solvomercurierungsreaktion der Cyclohexenole 3 und 4 liefert die cis/trans-Diole 1a bzw. reines trans-Diol 2a. Über die Monotosylate lassen sich das cis-Diol 2a sowie die cis-Aminoalkohole 1b und 2b diastereomerenrein durch SN2-Reaktionen mit KHCO3/18-Krone-6 bzw. KN3/18-Krone-6 und Reduktion mit LiAlH4 in guten Ausbeuten herstellen. NMR-spektroskopische Untersuchungen zeigen, daß in der cis-Reihe in aprotischen Medien die bisaxialen (cis-1-sc-sc) bzw. trisaxialen (cis-2-sc-sc) Konformationen - stabilisiert durch intramolekulare H-Brücken - vorliegen, während in protischen Medien die jeweiligen inversen Sesselkonformationen (cis-1-ap-ap bzw. cis-2-ap-ap) dominieren. Die konformativen Wechselwirkungen in den höher substituierten Cyclohexanderivaten 2 werden durch Röntgenstrukturanalyse eines cis- (cis-2b) und eines trans-Vertreters (trans-2a) untersucht.
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  • 2
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Multiple Bonds Between Main Group Elements and Transition Metals, XII. Generation and Complex Stabilization of Arsinidene and Diarsene Fragments by Complex-Induced Degradation of MonoarsaneThe Lewis base monoarsane is degraded in the presence of the solvens complex (η5-C5Me5)Mn-(CO)2THF (1; Me = CH3) to yield, under elimination of hydrogen, the arsinidene fragment AsH which latter species acts as a symmetrically bridging ligand in the novel dinuclear organometallic compound 2, thus forming a bent Mn, As, Mn′ three-center four-electron system (dMn — As = 224.7(1) pm, Mn — As — Mn′ = 139.3(1)°; single-crystal X-Ray structure analysis). The arsenic-hydrogen bond present in 2 is kinetically labile, allowing carbene insertion and As — As coupling reactions. Thus, treatment of 2 with diazoalkanes N2=CRR′ leads to N2-elimination and formation of the carbene insertion products (μ, η2-AsCHRR′)[(η5-C5Me5)Mn(CO)2]2 (3a - c); in these products, one of the two manganese-arsenic bonds originally present in the precursor compound 2 is bridged by the respective alkyl groups. Vacuum thermolysis of solid 2 cleanly proceeds at 120 - 140°C with climination of hydrogen and formation of the μ,η2-diarsane complex 4 that has a butterfly-type Mn2As2-structure with a very short As — As bond (dMn — As = 255.5 pm; av., dAs — As = 222.5(2) pm, double bond; no Mn — Mn bond; single crystal X-Ray structure analysis). Consecutive H2-elimination reactions are also observed when the THF complex 5 reacts with monoarsane; here, the tetranuclear diarsane complex 8 is formed which is structurally derived from coupling of two μ-arsinidene precursor species of type 6.
    Notes: Unter Wasserstoff-Eliminierung wird die Lewis-Base Monoarsan in Gegenwart des Solvens-Komplexes (η5-C5Me5)Mn(CO)2THF (1; Me = CH3) zum Arsiniden-Liganden AsH abgebaut, der in der neuen zweikernigen Komplexverbindung 2 als symmetrischer Brückenligand vorliegt und mit den beiden Metallatomen ein gewinkeltes Dreizentren-Vierelektronen-Bindungssystem bildet (dMn — As = 224.7(1) pm, Mn — As — Mn′ = 139.3(1)°; Einkristall-Röntgenstruktur-analyse). Die in 2 vorliegende Arsen-Wasserstoff-Bindung ist kinetisch labil und erlaubt Carben-Insertionen sowie As — As-Kupplungsreaktionen. Umsetzung mit Diazoalkanen N2=CRR′ ergibt unter N2-Eliminierung die Carben-Insertionsprodukte (μ, η2-AsCHRR′)[(η5-C5Me5)Mn-(CO)2]2 (3a - c) in denen eine der beiden Mangan-Arsen-Bindungen des Edukts 2 alkylverbrückt ist. Vakuumthermolyse von festem 2 bei 120 - 140°C führt unter H2-Abspaltung glatt zum μ,η2-Diarsen-Komplex 4, der eine Mn2As2-Butterfly-Struktur mit einer sehr kurzen As — As-Bindung besitzt (dMn — As = 255.5 pm, Mittelwert; dAs - As = 222.5(2) pm, Doppelbindung; keine Mn — Mn-Bindung; Einkristall-Röntgenstrukturanalyse). Konsekutive H2-Eliminierungsschritte begleiten auch die Reaktion des substitutionslabilen THF-Komplexes 5 mit Monoarsan zum vierkernigen Diarsen-Komplex 8, der als intermolekulares Kupplungsprodukt zweier μ-Arsiniden-Komplexvorstufen vom Typ 6 aufzufassen ist.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 118 (1985), S. 210-220 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Investigations on the Conformation and the Electronic Structure of CyclooctadienynesConformations and electronic structures of the cyclooctadienynes 1 and 2, predicted by semi-empirical quantum mechanics, are verified experimentally with the aid of 1H NMR and PE spectra. The results are correlated with those of other cycloalkynes 3-5 and cycloalkenes 6-11. In contrast to the decisive influence of the high geometrical ring strain in 1 and 2, homoaromaticity based on six almost planar π-electron centres is not significant.
    Notes: Die mit semiempirischer Quantenmechanik vorhergesagten Konformationen und elektronischen Strukturen der Cyclooctadienine 1 und 2 werden experimentell an Hand von 1H-NMR- und PE-Spektren verifiziert. Dabei wird Bezug genommen auf eine Reihe von anderen, verwandten Cycloalkinen 3-5 und Cycloalkenen 6-11. Während die hohe geometrische Ringspannung entscheidenden Einfluß auf 1 und 2 hat, ist eine Homoaromatizität, die auf sechs nahezu eben angeordneten π-Elektronen-Zentren beruht, nicht signifikant.
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  • 4
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Silicon Compounds with Strong Intramolecular Steric Interactions, 17. Disilenyl Anions \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm R}_{\rm 2} {\rm Si = }\,\left. {{\rm SiR}_{\rm 2} } \right]^{^{\mathop {\rm - }\limits_{\rm .} } } $\end{document} and Other Long-lived Silicon Centered RadicalsThe interaction of alkali metals with sterically congested 1,2-dihalo-1,1,2,2-tetraorganyldisilanes (2a-c) leads via the disilenes to the corresponding tetraorganyldisilenyl radical anions which have been characterized by their ESR spectra. The reaction of 1,2-dichloro-1,1,2,2-tetramesityl-disilane (3) with the tetraaminoethylene 5, however, yields a disilyl radical with a bridging chlorine atom (6). The preparation of several disilanes containing bulky ligands and the estimation of their conformations by variable-temperature NMR spectroscopy is described.
    Notes: Die Einwirkung von Alkalimetallen auf sterisch überladene 1,2-Dihalogen-1,1,2,2-tetraorganyldisilane (2a-c) führt über die Stufe der Disilene hinweg zu den entsprechenden Tetraorganyldisilenyl-Radikalanionen, die durch ihre ESR-Spektren charakterisiert werden. Dagegen liefert die Reaktion von 1,2-Dichlor-1,1,2,2-tetramesityldisilan (3) mit dem Tetraaminoethylen 5 ein chlorverbrücktes Disilyl-Radikal 6. Die Darstellung einiger Disilane mit sperrigen Liganden und die Abschätzung ihrer Konformation durch Tieftemperatur-NMR-Spektroskopie wird beschrieben.
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  • 5
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: Conformational energy profiles were calculated for τ1, the C—C—C=O torsion, and τ2, the C—C—C—C torsion, of methyl butanoate, using Pulay's ab initio gradient procedure at the 4-21G level with geometry optimization at each point. In addition, the structures of seven conformations were fully relaxed, including the energy minima (τ1, τ2) = (0, -60), (0, 180), (120, 180), (120, -60), and the maxima (0, 0), (180, 180), and (60, -60). The calculated geometries confirm the previously formulated rule that, in saturated hydrocarbons, a C—H bond trans to a C—C bond (C—Hs) is consistently shorter than a C—H bond (C—Ha) trans to another C—H bond. Specifically, for X—C(α) (= O)—C(β)—C(γ)—C(δ) systems, the following rules can be formulated, incorporating results from previous studies of butanal, butanoic acid, and 2-pentanone: (1) C(δ)—Hs 〈 C(δ)—Ha in all the conformers in which the δ-methyl group is remote from the ester group; whereas, in all the conformers in which nonbonded interactions are possible between the C(δ)-methyl and the ester groups, the bonding pattern is affected by a C—H⃛O=C interaction. (2) In the most stable conformers, (0, 60), C(β)—Ha 〈 C(β)—Hs, and C(γ)—Ha 〈 C(γ)—Hs, regardless of X. (3) The average C—C bonds in the τ2 = 180° conformers are consistently shorter than those with τ2 = 60° (compared at τ1 constant). In the most stable conformations (τ1 = 0°, τ2 = 60° or 180°), the bonding sequence is consistently C(α)—C(β) 〈 C(β)—C(γ) 〈 C(γ)—C(δ); whereas, when τ1 = 120°, C(α)—C(β) 〈 C(β)—C(γ) 〉 C(γ)—C(δ).
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 522 (1985), S. 108-116 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Sublimation Pressure of NbBr5, NbI5, and TaI5The sublimation pressure of NbBr5, NbI5 and TaI5 has been determined by a spectralphotometric method: \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{*{20}c} {{\rm log}\,{\rm P(NbBr}_{{\rm 5,}\,{\rm s}})\, = \, - \frac{{5240}}{{\rm T}}\, + \,8.66;} \hfill \\ {{\rm log}\,{\rm P(NbI}_{{\rm 5,}\,{\rm s}})\, = \, - \frac{{6762}}{{\rm T}}\, + \,8.566;} \hfill \\ {{\rm log}\,{\rm P(TaI}_{{\rm 5,}\,{\rm s}})\, = \, - \frac{{6938}}{{\rm T}}\, + \,9.38} \hfill \\ \end{array} $$\end{document}.The vapour pressure of NbI5,1 is equal to log \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm P}\,{\rm = }\, - \frac{{4653}}{{\rm T}}\, + \,5.43 $\end{document}. All the pressure are given in atm.The melting point of NbI5 is 673 ± 1 K.
    Notes: Der Sättigungsdruck von NbBr5, NbI5, und TaI5 wurde mit einer spektral- photometrischen Methode bestimmt; \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{*{20}c} {{\rm log}\,{\rm P(NbBr}_{{\rm 5,}\,{\rm f}})\, = \, - \frac{{5240}}{{\rm T}}\, + \,8,66;} \hfill \\ {{\rm log}\,{\rm P(NbI}_{{\rm 5,}\,{\rm f}})\, = \, - \frac{{6762}}{{\rm T}}\, + \,8,566;} \hfill \\ {{\rm log}\,{\rm P(TaI}_{{\rm 5,}\,{\rm f}})\, = \, - \frac{{6938}}{{\rm T}}\, + \,9,38} \hfill \\ \end{array} $$\end{document}.Der Dampfdruck von NbI5,fl ist log \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm P}\,{\rm = }\, - \frac{{4653}}{{\rm T}}\, + \,5,43 $\end{document}. Alle Drucke in atm.Der Schmelzpunkt von NbI5 liegt bei 673 ± 1 K.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 522 (1985), S. 99-107 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Vapour Pressure of NbCl4 and NbBr4The vapour pressur of solid NbCl4 has been determined spectralphotometrically near 600 K: \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{*{20}c} {{\rm log}\,{\rm P}({\rm NbCl}_4,\,60{\rm 0}\,{\rm K})\, = \, - \frac{{5937}}{{\rm T}}\, + \,7.931.} \hfill \\ {\Delta {\rm H}^ \circ {\rm (subl}{\rm .,}\,{\rm 298}\,{\rm K)}\,{\rm = }\,{\rm 28696}\,{\rm cal/Mol;}\,\Delta {\rm S(subl}{\rm .,}\,{\rm 298}\,{\rm K)}\,{\rm = }\,{\rm 40}{\rm .10}\,{\rm eu;}} \hfill \\ {\Delta {\rm Cp}\, = \, - 6.1\, + \,0.9 \times \,10^5 {\rm T}^{{\rm - 2}} } \hfill \\ \end{array} $$\end{document}.NbCl4 is monomolecular in the gaseous state.In the same way the vapour pressure of NbBr4 has been found: \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm log}\,{\rm P}({\rm NbBr}_4,\,626\,{\rm K})\, = \, - \frac{{6722}}{{\rm T}}\, + \,9.057 $$\end{document}.
    Notes: Der Sättigungsdruck von festem NbCl4 wurde spektralphotometrisch bei Temperaturen um 600 K gemessen: \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{*{20}c} {{\rm log}\,{\rm P}({\rm NbCl}_4,\,60{\rm 0}\,{\rm K})\, = \, - \frac{{5937}}{{\rm T}}\, + \,7,931.} \hfill \\ {\Delta {\rm H(subl}{\rm .,}\,{\rm 298}\,{\rm K)}\,{\rm = }\,{\rm 28696}\,{\rm cal/Mol;}\,\Delta {\rm S(subl}{\rm .,}\,{\rm 298}\,{\rm K)}\,{\rm = }\,{\rm 40,10}\,{\rm eu;}} \hfill \\ {\Delta {\rm Cp}\, = \, - 6,10\, + \,0,9\, \cdot \,10^5 {\rm T}^{{\rm - 2}} } \hfill \\ \end{array} $$\end{document}.Gasförmiges NbCl4 ist monomolekular.Auf gleiche Weise wurde der Sättigungsdruck von festem NbBr4 gemessen: \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm log}\,{\rm P}({\rm NbBr}_4,\,626\,{\rm K})\, = \, - \frac{{6722}}{{\rm T}}\, + \,9,057 $$\end{document}.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 524 (1985), S. 83-89 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On Chalcogenidosilicates: Ba2SiTe4 and Ba2SiSe4The new compounds Ba2SiSe4 and Ba2SiTe4 crystallize in the monoclinic system, space group: P21/m (No. 11) with the lattice constants s. “Inhaltsübersicht”. Both compounds are isotypic to the Sr2GeS4 structure. Ba2SiTe4 is the first o-telluridosilicate with discrete SiTe44- anions.
    Notes: Die neuen Verbindungen Ba2SiSe4 und Ba2SiTe4 kristallisieren monoklin (Raumgruppe: P21/m, Nr. 11) in der Sr2GeS4-Struktur mit den GitterkonstantenBa2SiSe4: a = 918,4(5) pm, b = 703,3(3) pm, c = 687,2(3) pm, β = 109,2(1)°Ba2SiTe4: a = 965,0(5) pm, b = 762,6(3) pm, c = 746,6(3) pm, β = 108,9(1)°Ba2SiTe4 ist das erste ortho-Telluridosilicat, d. h. es treten diskrete SiTe44--Anionen auf.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 524 (1985), S. 137-143 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reaction of [Mo6Cl8]X4 with N-Bases[Mo6Cl8]X4 (X = Cl, Br, I) in ethanol solution by titration with Ag+ showed 4 labil X atoms. The displacement of X- especially by F- accelerates the titration decisively. Conductivity measurements in ethanol or acetone showed that [Mo6Cl8]X4 at 25°C behave as weak 1:1-electrolytes. Solutions of [Mo6Cl8]X4 in DMF heated up to 60°C and than lowered to 25°C showed that the compounds in this solvent behave as (potential) strong 2:1-valent electrolytes.From the following compounds the labil halides have been determined by titration with Ag+: [Mo6Cl8]X4(Py)2 (X = Cl, Br), [Mo6Cl8]X4(bipy)2 (X = Cl, Br, I), [Mo6Cl8]X4(Phenpy)2 (X = Cl, Br, I), (PyH)2[Mo6Cl8]X6 (X = Cl, Br); (bipyH)2[Mo6Cl8]I4Cl2. Always 4 (respectively 6) labil halides have been observed; exception [Mo6Cl8]Cl4(Py)2 in acetone (2 labil Cl).Lattice constants and mole volumina for the adducts with pyridin and bipyridin have been determined. The adducts with bipyridin and phenylpyridin are isotypic.Conductivity measurements have been made in different solutions.The decomposition on the thermobalance showed that in [Mo6Cl8]Cl4(Py)2 the bond of pyridin is weak. The 2 pyridin molecules are evolved at the same time. However [Mo6Cl8]I4(Bipy)2 loses 1 bipyridin only.(PyH)2[Mo6Cl8]X6 formed during the first decomposition step the novel compounds (PyH) [Mo6Cl8]X5 (X = Cl, Br). Both compounds are isotypic. They behave in ethanol solution as strong 1:1-valent electrolytes.
    Notes: [Mo6Cl8]X4 (X = Cl, Br, I) lieferte in ethanolischer Lösung bei der Titration mit Ag+ 4 labile X. Dabei förderte die Verdrängung von X- insbesondere mit F- die Geschwindigkeit der Reaktion entscheidend. Bei Leitfähigkeitsmessungen in Ethanol oder Aceton verhält sich [Mo6Cl8]X4 bei 25°C als schwacher 1:1 wertiger Elektrolyt. Lösungen in DMF auf 60°C erhitzt und dann bei 25°C gemessen, zeigten, daß sich die Verbindungen [Mo6Cl8]X4 in diesem Lösungsmittel als (potentiell) starke 2:1 wertige Elektrolyte verhalten.In den folgenden Verbindungen wurden die labilen Halogene durch potentiometrische Titration mit Ag+ bestimmt: [Mo6Cl8]X4(Py)2 (X = Cl, Br), [Mo6Cl8]X4(bipy)2 (X = Cl, Br, I), [Mo6Cl8]X4 (Phenpy)2 (X = Cl, Br, I), (PyH)2[Mo6Cl8]X6 (X = Cl, Br); (bipyH)2[Mo6Cl8]I4Cl2. Stets wurden 4 (bzw. 6) labile Halogene gefunden, Ausnahme [Mo6Cl8]Cl4(Py)2 in Aceton (2 labile Cl).Gitterkonstanten und Molvolumina wurden für die Pyridin- und Bipyridin-Addukte bestimmt. Die Addukte mit Bipyridin und Phenylpyridin sind isotyp.Leitfähigkeiten wurden für die verschiedenen verdünnten Lösungen bestimmt.Der Abbau an der Thermowaage zeigte, daß in [Mo6Cl8]Cl4(Py)2 2 Pyridin locker gebunden sind und gleichzeitig abgegeben werden. Dagegen verlor [Mo6Cl8]I4(bipy)2 an der Thermowaage nur 1 Bipyridin.(PyH)2[Mo6Cl8]X6 bildete in erster Abbaustufe die neuen Verbindungen (PyH)[Mo6Cl8]X5 (X = Cl, Br). Beide Verbindungen sind isotyp. Sie sind in Ethanol starke 1:1 wertige Elektrolyte.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 530 (1985), S. 74-78 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Ca5Sn2As6, The First Inoarsenidostannate(IV)The new compound Ca5Sn2As6 crystallizes in the orthorhombic system (space group Pbam (No. 55)) with the lattice constants s. „Inhaltsübersicht“. In the structure SnAs4-tetrahedra are connected by common corners to „Einereinfach“ chains. The compound belongs to the “Zintlphases”.
    Notes: Die neue Verbindung Ca5Sn2As6 kristallisiert orthorhombisch in der Raumgruppe Pbam (Nr. 55) mit den Gitterkonstanten a = 1 364,3(8) pm, b = 1 183,0(6) pm, c = 412,1(4) pm.In der Struktur sind SnAs4-Tetraeder über gemeinsame Ecken zu „Einereinfachketten“ verknüpft. Die Verbindung gehört zu den „Zintlphasen“.
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