ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Halogenocyclotetraphosphanes  (1)
  • 1995-1999  (1)
  • 1
    ISSN: 0044-2313
    Keywords: Phosphanediyl ; Halogenocyclotetraphosphanes ; NMR Crystal Structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: In situ Generation of [PX] and Insertion into (tBuP)3, (X = Cl, Br). Synthesis of the Functionalized Cyclophosphanes (tBuP)3PX, [1-(tBu)(X)P-2,3,4-(tBu)3]P4 and Structure Analysis of (tBuP)3PClThe redox system PX3/SnX2 (X = Cl, Br) can be used as a source for the in situ generation of halogenphosphanediyl [PX]. In the presence of tri-t-butylcyclotriphosphane (tBuP)3 the intermediately formed [PX] is added to a ring P atom followed by an insertion reaction, which leads to a ring expansion, whereby monohalogenocyclotetraphosphanes (tBuP)3PX (X = Cl, Br; 1, 2) are formed. Excess [PX] does not lead to further ring expansion but through a complex reaction course to the functionalized cyclotetraphosphanes [1-(tBu)(X)P-2,3,4-(tBu)3]P4, 3 (X = Br); 7 (X = Cl). 1, 2 and 3 could be obtained in a pure form and NMR and mass spectroscopically, 7 31P-NMR spectroscopically, characterized. For 1 and 7 31P—35,37Cl-isotopic shifts could be identified. 1 was further characterized by an X-ray structure analysis.
    Notes: Das Redoxsystem PX3/SnX2 (X = Cl, Br) kann als Quelle zur in situ-Bildung von Halogenphosphandiyl [PX] verwendet werden. In Gegenwart von Tri-t-butylcyclotriphosphan (tBuP)3 wird intermediär auftretendes [PX] zuerst an ein Ring-P-Atom addiert, dann unter Ringexpansion insertiert, wobei Monohalogenocyclotetraphosphane (tBuP)3PX (X = Cl, Br; 1, 2) gebildet werden. Überschüssiges [PX] führt nicht zu einer weiteren Ringexpansion; vielmehr entstehen in einem komplexen Reaktionsverlauf die funktionalisierten Cyclotetraphosphane [1-(tBu)(X)P-2,3,4-(tBu)3]P4, 3 (X = Br); 7 (X = Cl). 1, 2 und 3 konnten in reiner Form isoliert und NMR- sowie massenspektroskopisch, 7 31P-NMR-spektroskopisch, charakterisiert werden. Bei 1 und 7 konnten 31P—35,37Cl-Isotopieverschiebungen nachgewiesen werden. Von 1 wurde eine Röntgenstrukturanalyse durchgeführt.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...