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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 11 (1978), S. 424-426 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 12 (1984), S. 331-335 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Multiblock copolymers of styrene and α-methylstyrene (¯Mn ≦ 70.000 g.mole−1) with various α-methylstyrene contents were synthetized by anionic polymerization. The glass transition temperatures (Tg) of these copolymers have been measured by D.T.A. A single Tg was observed over the whole composition range. This Tg obeys the derived GORDON and TAYLOR equation. Moreover these copolymers are heat resistant up to temperatures of at least 280°C.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 54 (1994), S. 1439-1447 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Owing to the low Tg of polystyrene, the mechanical properties of polystyrene-block-poly-butadiene-block-polystyrene (SBS) thermoplastic elastomers drop steeply above 60°C. To overcome this behavior, many research groups have considered the replacement of styrene (S) by α-methylstyrene (MS). We also attempted the synthesis of copolymers with a central polybutadiene (poly B) block and rigid blocks consisting of polystyrene (poly S) and poly(α-methylstyrene) (poly MS) blocks. Starting from a dilithium initiator, difunctional poly B's with low 1,2 content (10%) were prepared and toluene was added. After addition of a small amount of styrene, MS was added in the presence of a 15% (in vol) of THF at T ≤ -40°C. The copolymers did not have the expected structure and poor mechanical properties resulted, which were, however, still measurable at 120°C. These results probably resulted from secondary reactions involving the MS carbanions. To identify these reactions and to control the polymer structure, the synthesis of multiblock copolymers was carried out with a monofunctional polybutadienyllithium to which were added successively S and MS (in a mixture of hexane and benzene as solvent). MS was added at low temperature in the presence of small amounts of THF or at room temperature after addition of TMEDA. These attempts were unsuccessful, the copolymer being always multimodal as a result of unwanted coupling reactions involving terminal double bonds. The synthesis of elastomers using a coupling reaction of poly MS-poly S-poly B was also considered but the yield in poly B was low since termination reactions involving the polar additive occurred. © 1994 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 15 (1977), S. 2373-2379 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A kinetic study in tetrahydrofuran of the addition of 1,1-diphenylethylene on para-substituted styrylcarbanions (with Cs+ as counterion) has given the reactivities of free ions and ion-pairs. For both species, the addition rate constant increased in the following sequence for the substituent of the phenyl ring: pH 〈 p-CH3 〈p-CH3O. It was also shown that in the same solvent, the dissociation constants of the polystyryl ion-pairs decreased with the electron-donating power of the substituent.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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