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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 1209-1232 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The terpolymerization of ethylene, propylene, and methylcyclopentadienyl-5-endonorborn-2-enylmethane (III) by means of different vanadium-based coordination catalysts was investigated. The structure of III and its isomeric composition was studied by using vapor-phase chromatography, mass spectrometry, and NMR, infrared, and ultraviolet spectroscopy. The catalyst system V Acac3-Et2AlCl was used under different conditions, and the influence of several variables regulating the terpolymerization process were related to the properties of the resulting terpolymers (EPTM). The insertion of III into EPTM chains takes place randomly and does not influence the random distribution of comonomers. The selective opening of the norbornene double bond of III has been demonstrated by use of 2,3-dihydro-III as model compound. Tritiated III gave a radiochemical titer of unsaturation in excellent agreement with the value deduced from ultraviolet measurements. The influence of Lewis bases added to VAcac3-Et2AlCl catalyst is discussed.
    Additional Material: 19 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 9 (1971), S. 1575-1598 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A detailed investigation of the terpolymerization reaction of ethylene and propylene with 1-isopropylidene-dicyclopentadiene (II) was carried out by empolying vanadiumbased anionic coordinate catalysts [preferentially V(Acac)3—AlEt2Cl]. The influence of some polymerization parameters, i.e., concentration of II, of the catalyst; polymerization time, etc., were particularly examined. The catalysts were found to be active in C2H4—II copolymerization also, but neither C3H6—II copolymer nor II homopolymer were obtained. By using the 5,6-dihydro derivative of II as comonomer, it was found through ultraviolet, infrared, and NMR analyses that the incorporation of II in polyethylene or ethylene-propylene chains took place randomly and by selective opening of the norbornene double bond. The quantitative determination of the unsaturation present in C2H4—C3H6—II terpolymer was studied by means of absorption of iodine halides and through a spectroscopic ultraviolet method. Reference was made to terpolymer samples containing 14C-labeled II. The content of II was generally less than 35 wt-% both in copolymer and in terpolymer prepared. The relatively high reactivity of II is discussed in terms of norbornene ring strain and compared with the reactivity of 1-isopropylidene-3a,4,7,7a-tetrahydroindene (I) previously reported.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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