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Alkene Polymerization Ti, Zr, Sc, and others

The catalytic cycle for alkene polymerization, the Cossee mechanism, is extremely simple. Coordination of the alkene to Cp2ZrR+ is followed by insertion to give a new complex Cp2ZrR+. No change in the oxidation state of Zr occurs in either of these steps. [Pg.288]

There are several mechanisms for termination of the growing polymer chain. One common chain termination step is jS-hydride elimination to give Cp2ZrH+ and the polymer with a terminal double bond. When the polymerization is carried out under H2, a cr-bond metathesis can take place to give the saturated polymer and Cp2ZrH +.  [Pg.289]

When alkenes higher than ethylene are polymerized, regio- and stereochemical issues arise. The regiochemical issue arises when the alkene H2C=CHR in- [Pg.289]

Problem. 6.5. When alkenes are subjected to polymerization conditions in the presence of a sufficiently high concentration of H2 gas, alkene hydrogenation occurs instead of polymerization. Draw a reasonable mechanism for this transformation. [Pg.290]


See other pages where Alkene Polymerization Ti, Zr, Sc, and others is mentioned: [Pg.288]    [Pg.282]   


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