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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 458 (1979), S. 318-320 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Ultra-Purification of Oligomeric ChlorocyclophosphazenesChlorocyclophosphazenes are obtained usually as a mixture of different ring size oligomers. Isolation of the raw oligomeric species may be performed easily, while their ultrapurification is a rather difficult operation. For special requirements, ultrapure oligomeric chlorocyclophosphazenes may be obtained by a high-yield zone-melting procedure.
    Notes: Die applikativ und theoretisch bedeutenden oligomeren Chlorcyclophosphazene fallen bei den klassischen Syntheseverfahren als Komponenten eines Gemisches verschiedener Ringgrößen an. Während eine Isolierung der einzelnen Spezies in rohem Zustand im allgemeinen keine Schwierigkeiten bereitet, ist ihre Reinstdarstellung nicht unproblematisch. Die manchmal erforderlichen hochgereinigten Verbindungen sind mit geringem Aufwand im Zonenschmelzverfahren zugänglich.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 435 (1977), S. 98-102 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Chalcogenolates and their Derivatives. I. Syntheses and Properties of Ionic ChalcogenophenolatesThe syntheses and properties of ionic chalcogenophenolates are described. Using liquid ammonia as solvent the alkali chalcogenophenolates M[EPh] (M = Na, K; E = Se, Te; Ph = C6H5) have been synthesized via reduction of the diphenyl dichalcogenides with alkali metals. Similarly, the tetraphenylphosphonium chalcogenophenolates [Ph4P][EPh] (E = S, Se, Te) have been obtained by reacting alkali chalcogenophenolates with tetraphenylphosphonium chloride.
    Notes: Darstellung und Eigenschaften salzartiger Chalkogenolate werden beschrieben. In verflüssigtem Ammoniak als Lösungsmittel lassen sich die Alkalichalkogenophenolate M[EPh] (M = Na, K; E = Se, Te; Ph = C6H5) durch Spaltung der Diphenyldichalkogenide mit Alkalimetallen, die Tetraphenylphosphoniumchalkogenophenolate [Ph4P][EPh] (E = S, Se, Te) durch doppelte Umsetzung der Alkalichalkogenophenolate mit Tetraphenylphosphoniumchlorid erhalten.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 436 (1977), S. 283-288 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Hydrogen-bonded Dimerisation of Several P-oxo-N-hydro-cyclophosphazenes1,3,3,5,5-Pentamethoxy-1-oxo-2-hydro-cyclotriphosphazadiene and 1,3,3,5,5,7,7-heptamethoxy-1-oxo-2-hydro-cyclo-tetraphosphazatriene are hydrogen-bonded dimers in solutions of low polarity. Partial dissoziation of these dimers occurs e. g. in chloroform. Monomeric and dimeric species may be properly quantitated by infrared spectroscopy in deuterochloroform. Equilibrium constants and dissociation enthalpies were determined.
    Notes: 1,3,3,5,5-Pentamethoxy-1-oxo-2-hydro-cyclotriphosphazadien und 1,3,3-,5,5,7,7-Heptamethoxy-1-oxo-2-hydro-cyclotetraphosphazatrien liegen in Lösungen geringer Polarität als doppelt wasserstoffverbrückte Dimere vor. In Chloroform sind diese teilweise dissoziiert. Monomeres und Dimeres können infrarotspektroskopisch in Deuterochloroform quantitativ erfaßt werden. Gleichgewichtskonstanten und Dissoziationsenthalpien wurden auf diesem Wege ermittelt.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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