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  • Polymer and Materials Science  (2)
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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 2993-3000 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The oxidation of poly(styryl)lithium with molecular oxygen was investigated in the solid state (with and without N,N,N′, N′-tetramethylethylenediamine) in benzene (with and without N,N,N′, N′-tetramethylethylenediamine) and in benzene/tetrahydrofuran (THF) solutions. The oxidation products included the corresponding polystyrene dimer [(PS)2], the dimeric poly(styrene) peroxide (PSO2PS), poly(styrene) hydroperoxide (PSO2H), and the hydroxyl-terminated polymer (PSOH). The hithertofore unreported macroperoxide (PSO2PS) accounts for approximately 50% of the dimeric product obtained from poly(styryl)lithium oxidations in the presence of Lewis bases. The total amount of peroxide products was determined by iodometric titration in the presence of a phase-transfer catalyst, dicyclohexyl-18-crown-6. On the basis of the effect of polar additives on the amount of dimeric products, it is concluded that dimer formation in the air termination of polymeric organolithium compounds results from oxidation and not carbonation reactions.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 183 (1982), S. 2071-2076 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The carbonation reactions of polymeric organolithium compounds with high purity, gaseous carbon dioxide have been investigated in benzene and benzene/tetrahydrofuran (75/25) solutions. The polymers investigated were poly(styryl)lithium, poly(isoprenyl)lithium, and poly(styrene-b-isoprenyl)lithium. In Benzene solution the products are a mixture of the carboxylic acid and the ketone (dimer). No tertiary alcohol product (trimer) was observed. In benzene/tetrahydrofuran solution, the quantitative carboxylation of chain ends was observed.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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