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Ring opening polymerization polyisoprene

PMPS-Z -PS and PMPS-/ -Pl were synthesized by the anionic ring-opening polymerization of tetramethyltetraphenylcyclotetrasilane (prepared from commercially available octaphenyltetrasilane) initiated by the living anionic chain ends of polystyrene and polyisoprene [52, 53] (Fig. 4b). [Pg.254]

Photoinitiated Ring-Opening Polymerization of Epoxidized Polyisoprene... [Pg.286]

The discovery of the anionic ring-opening polymerization of silicon-bridged[l]ferrocenophanes enabled the synthesis of well-defined, near-monodisperse poly(ferrocenylsilane) homo- and block copolymers. PFS was combined with polystyrene [38], polyisoprene [39], poly(dimethylsilox-ane) [40], poly(ethylene oxide) [41], poly(ferrocenylphenylphosphine) [42], poly(aminoalkyl methacryate) [43] and recently with poly(methyl methacrylate) [44,45] blocks. [Pg.93]

Polyisoprene-Z)/oc -polyferrocenyldimethylsilane (PI-i-PFDMS) was synthesized by the anionic ring-opening polymerization of 1 initiated by living polyisoprene prepared inTHF (Scheme 1). The products were recovered as amber gumlike materials. [Pg.88]

It is noteworthy that poly(l-methylbutenamer) obtained by ring-opening metathesis polymerization has the structure of 1,4-polyisoprene, a well known elastomer of high commercial value. [Pg.106]

Z/E Isomerism (generally indicated by cis/trans). This is found in polymers obtained from conjugated dienes or by ring-opening metathesis polymerization of cycloalkenes (polyalkenamers). The example illustrated hereafter is that of 1,4-polyisoprene (or 2-methylbuta-l,3-diene). It is important from an economical point of view—in particular, in the industry of natural and synthetic elastomers. [Pg.32]


See other pages where Ring opening polymerization polyisoprene is mentioned: [Pg.17]    [Pg.429]    [Pg.297]    [Pg.429]    [Pg.502]    [Pg.4351]    [Pg.76]    [Pg.499]    [Pg.147]    [Pg.190]    [Pg.106]    [Pg.171]   


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