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  • 1995-1999  (1)
  • 1975-1979  (1)
  • Chemistry  (2)
  • 1
    ISSN: 0044-2313
    Keywords: Diphosphene dimerization ; Ylide substituents, Cyclotetraphosphine structure, 31P-NMR spectra analysis, Transanular electron lone pair interaction ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: 1,3-Bis(triphenylphosphonium-ylidyl)cyclotetraphosphinesThe title compounds 3a, b result from the condensation of the ylidyldichlorophosphines Ph3PCR—PCl2 1a, b (R = Me, 3-Tol) with phenyl bis(trimethylsilyl)phosphine 2. Analysis of the 31P-NMR spectra and the X-ray structure investigation of 3a demonstrate a folding of the four-membered ring and an all-trans orientation of the substituents.
    Notes: Die Titelverbindungen 3a, b entstehen durch Kondensation der Ylidyldichlorphosphane Ph3PCR—PCl2 1a, b (R = Me, 3-Tol) mit Phenyl-bis(trimethylsilyl)phosphan 2. Die Analyse der 31P-NMR-Spektren und die Röntgenstrukturbestimmung von 3a zeigen eine Faltung des Vierrings und all-transständige Substituenten.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Phosphazenes. LXVI. 31P-NMR Investigations. XI. Preparation of Cyclotri(phosphazene) Derivatives via the Corresponding Lithium Compound and Spreading of a 31P-NMR Spectrum by a Shift ReagentLess reactive partners such as phosphinyl chlorides do not react with the hydridocyclotri(phosphazene) I, but they react with the lithiated phosphazene II giving P-substituted products. Silyl-, stannyl-, imidophosphinyl- and thiophosphinylcyclotri(phosphazenes) have been prepared as examples. In the dimethylthiophosphinyl derivative VI the two 31P nuclei of the biphosphine grouping are nearly isochronous and their n.m.r. signals as well as those of the methyl protons are therefore degenerate. Using a shift reagent the shift difference can be increased by more than a factor of ten and the degeneracy removed.
    Notes: Mit weniger elektrophilen Partnern wie Phosphinylchloriden kann das Hydridocyclotri(phosphazen) I nicht mehr direkt, wohl aber nach Überführung in seine Lithiumverbindung II am Phosphor substituiert werden. Als Beispiele wurden Silyl-, Stannyl-, Imidophosphinyl- und Thiophosphinylcyclotri(phosphazene) dargestellt. Im Dimethylthiophosphinylderivat VI sind die beiden 31P-Kerne der Biphosphingruppierung nahezu isochron und ihre NMR-Signale und die der Methylprotonen deshalb entartet. Durch ein Shiftreagens kann ihre Verschiebungsdifferenz mehr als verzehnfacht und die Entartung damit aufgehoben werden.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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