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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 417 (1975), S. 161-170 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The Reaction of Cyclophosphanes with Carbon Tetrachloride and AminesThe cleavage of phenylcyclophosphanes with carbon tetrachloride leads to the chloro-trichloromethyl-phosphine 2a; tetracyclohexycyclotetraphosphine decomposes in the same manner to the diphosphane 3. Methyl-and ethylcyclophosphanes give with carbon tetrachloride the monoquaternary salts 4c and 4d. The cleavage products 5, 2d and 6 are also formed. The tris-(amino)-phosphonium salts 7a-j and the chloromethylphosphonium chloride 8a are obtained by reaction of amines with cyclophosphanes and carbon tetrachloride. All phosphonium chlorides are isolated and charakterized as perchlorates.
    Notes: Phenylcyclophosphane werden durch Tetrachlorkohlenstoff zum Chlor-trichlormethyl-phosphin 2a, Tetracyclohexylcyclotetraphosphan zum Diphosphan 3 abgebaut. Methyl-und Äthylcyclophosphane bilden mit Tetrachlorkohlenstoff die monoquartären Salze 4c bzw. 4d. Daneben entstehen die Spaltprodukte 5 bzw. 2d und 6. Durch die Einwirkung von Aminen auf Cyclophosphane und Tetrachlorkohlenstoff werden die Tris(amino)-phosphoniumsalze 7a,/-j und das Chlormethylphosphoniumchlorid 8a erhalten. Alle Phosphoniumchloride werden als Per-chlorate isoliert und charakterisiert.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 429 (1977), S. 69-73 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Hydrofluorination of Bis(silylimido)tetramethyldiphosphoraneThe silylated bis(imidophosphorane), (CH3)2P[NSi(CH3)3]—P[NSi(CH3)3](CH3)2, 1 reacts in ether with hydrogen fluoride to give the tetrafluorodiphosphorane, (CH3)2PF2—PF2(CH3)2, 2, while hydrofluorination in fluorotrichloromethane gives the diazadiphosphetidin 3 and the iminophosphorane 4. The thermal decomposition of 2, studied by 19F and 31P-n.m.r. spectroscopy, yields trifluorodimethylphosphorane and tetramethyldiphosphane.
    Notes: Das silylierte Bis(imidophosphoran), (CH3)2P[NSi(CH3)3]—P[NSi(CH3)3] (CH3)2, 1 wird durch ätherischen Fluorwasserstoff in das Tetrafluordiphosphoran, (CH3)2PF2—PF2(CH3)2, 2 überführt, während die entsprechende. Hydrofluorierung in Fluortrichlormethan das N-Trimethylsilylfluordimethyl-diazadiphosphetidin 3 und Fluordichlormethyl-dimethyl-N(trimethylsilyl)iminophosphoran 4 liefert. 2 ist thermisch labil und zerfällt in Trifluordimethylphosphoran und Tetramethyldiphosphan.
    Type of Medium: Electronic Resource
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