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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 3205-3213 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics and mechanisms of propadiene polymerization under the influence of [Rh(CO)2Cl]2, Rh(CO)2P(C6H5)3Cl, Rh(CO)3Cl are reported. The reaction rates are first-order in Rh(CO)2P(C6H5)3Cl and Rh(CO)3Cl and half-order in [Rh(CO)2Cl]2. They are second-order in the substrate for Rh(CO)3Cl and [Rh(CO)2Cl]2 and first-order for Rh(CO)2P(C6H5)3Cl. The data are interpreted in terms of a common intermediate mechanism. The formation of this common intermediate is the rate-determining step. A solvent effect is also discussed.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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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. 2395-2402 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A literature survey is given of the methods of preparation of 1,2-and 1,2,2,1-polyallene. The spectroscopic data and other physico-chemical properties are compiled. Spectral analysis of the products in relation to the catalyst used leads to conclusions with regard to the effect of electron-donating and electron-withdrawing ligands to the transition metal of the catalyst on the ratio of 1,2 to 1,2,2,1-polyallene structural units in the polymer obtained. This hypothesis enabled us to prepare a structurally homogeneous 1,2 polyallene in almost quantitative yield. The catalyst was prepared by adding propadiene to a benzene solution of Ni(II) acetylacetonate followed by addition of triisobutylaluminum. This sequence of addition appeared to be the essential factor for obtaining an active catalyst. A kinetic scheme for the polymerization is put forward.
    Additional Material: 6 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 10 (1972), S. 3067-3076 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polymerization of propadiene to 1,2-polyallene by various Rh(I) based catalysts is described and discussed. Also the interrelations between these Rh(I) complexes are discussed and an overall reaction scheme is given. A mechanism is put forward in which the formation of a common intermediate from propadiene and different Rh(I) complexes is the rate determining step. It is found that the activity decreases in the order: cis-Rh(CO)2P(C6H5)3Cl 〉 [Rh(CO)2Cl]2 〉 Rh(CO)3Cl. The complexes Rh[P(C6H5)3]2(CO)Cl and Rh[P(C6H5)3]3Cl proved to be inactive in the polymerization of propadiene.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 9 (1971), S. 2403-2407 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A variety of catalyst systems based on 3d transition metals, i.e., V(III), Cr(III), Mn(II), Fe(II), Co(II), Ni(II), Cu(II), and various stabilizing ligands, i.e., propadiene, methylacetylene, phenylacetylene, and 1,4-butadiene, were prepared. The activity of these catalytic systems towards the polymerization of a series of monomers (propadiene, methylacetylene, phenylacetylene, 1,4-butadiene, ethene, and propene) is investigated. Optimum conditions for the preparation of 1,2-polyallene, polymethylacetylene and polyphenylacetylene are given.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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