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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1975 (1975), S. 509-520 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reactions between Benzyl Derivatives of Titanium and AluminiumThe reaction between tribenzylaluminium (AlBz3) and tetrabenzyltitanium (TiBz4) or tris(p-methylbenzyl)aluminium (AlXy3) and tetrakis(p-methylbenzy1)titanium (TiXy4) with elimination of toluene or xylene respectively, which yields catalytic systems for α-olefin polymerization, has been investigated using cryoscopy, MS, and 1H-NMR spectroscopy. The extent of the reaction depends on the Al/Ti ratio, reaching a maximum for values between 4 and 5. The reaction is accompanied by a reduction of Ti(IV) to Ti(III). On mixing tetrabenzyltitanium (TiBz4) with dibenzylzinc (ZnBz2) [Zn/Ti = 1.23] only titanium reduction occurs. This system does not polymerize 4-methyl-1-pentene.
    Notes: Die Reaktion zwischen Tribenzylaluminium (AlBz3) und Tetrabenzyltitan (TiBz4) oder Tris(p-methylbenzyl)aluminium (AlXy3) und Tetrakis(p-methylbenzyl)titan (TiXy4) unter Eliminierung von Toluol bzw. Xylol, welche katalytische Systeme für die Polymerisation von α-Olefinen liefert, wurde durch Kryoskopie, MS- und 1H-NMR-Spektroskopie untersucht. Das Reaktionsausmaß hängt von dem Al/Ti-Verhältnis ab und erreicht ein Maximum für Al/Ti zwischen 4 und 5. Die Reaktion wird von einer Reduktion von Ti(IV) zu Ti(III) begleitet. Beim Mischen von Tetrabenzyltitan (TiBz4) mit Dibenzylzink (ZnBz2) [Zn/Ti = 1.23] findet nur die Reduktion des Titans statt. Dieses System polymerisiert 4-Methyl-1-penten nicht.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 58 (1975), S. 1512-1517 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The cyclisation of either 1a or 3a with acid yielded the cis-fused erythrinanone 2; no trans-isomer could be detected. The structure of this unexpected product was determined by NMR. and confirmed by an X-ray analysis. Various tetrahydro- and hexahydro-2-indolinones were prepared to facilitate the interpretation of the NMR.-spectrum of 2.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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