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Alkene Ziegler-Natta polymerization

The preparation and structure determination of ferrocene marked the beginning of metallocene chemistry Metallocenes are organometallic compounds that bear cyclo pentadiemde ligands A large number are known even some m which uranium is the metal Metallocenes are not only stucturally interesting but many of them have useful applications as catalysts for industrial processes Zirconium based metallocenes for example are the most widely used catalysts for Ziegler-Natta polymerization of alkenes We 11 have more to say about them m Section 14 15... [Pg.610]

Alkene polymerization can be carried out in a controlled manner using a Ziegler-Natta catalyst. Ziegler-Natta polymerization minimizes the amount of chain branching in the polymer and leads to stereoregular chains—either isotactic (substituents on the same side of the chain) or syndiotactic (substituents on alternate sides of the chain), rather than atactic (substituents randomly disposed). [Pg.1220]

The mechanistic similarity between Ziegler-Natta polymerization of olefins and the alkene cyclization reactions described above suggested that early transition metal catalysts would be effective catalysts for the coupling of... [Pg.237]

Aside from the Ziegler-Natta polymerization, alkene and alkyne metathesis, and other reactions of Ti-methylene complexes, carbometallation reactions induced by alkyltitanium compounds have been dominated by those involving... [Pg.259]

Ziegler-Natta polymerization leads to linear unbranched polyethylene, the so-called high density polyethylene (HDPE), which is denser, tougher and more crystalline. By copolymerization with other alkenes it is possible to obtain linear low density polyethylene (LEDPE) with better mechanical properties than LDPE. Blends of LLDPE and LDPE are used to combine the good final mechanical properties of LLDPE and the strength of LDPE in the molten state. [Pg.218]

TRADITIONAL ZIEGLER-NATTA POLYMERIZATION OF NONPOLAR ALKENE MONOMERS... [Pg.644]

When ethylene reacts with triethyl- or tripropylaluminum, multiple carbometa-lation takes place, resulting in the formation of oligomers.509 Oxidation of the products followed by hydrolysis yields alcohols, whereas displacement reaction produces terminal alkenes that are of commercial importance.510 Transition-metal compounds promote the addition to form polymers (Ziegler-Natta polymerization see Section 13.2.4). [Pg.331]

Cyclization of alkenes.1 This Ziegler-Natta polymerization catalyst can effect intramolecular cyclization of unactivated alkenes. Thus transmetallation of a Grignard reagent (1) with Cp2TiCl2 results in a titanium complex (2), which on... [Pg.117]

Migratory insertion is the principal way of building up the chain of a ligand before elimination. The group to be inserted must be unsaturated in order to accommodate the additional bonds and common examples include carbon monoxide, alkenes, and alkynes producing metal-acyl, metal-alkyl, and metal-alkenyl complexes, respectively. In each case the insertion is driven by additional external ligands, which may be an increased pressure of carbon monoxide in the case of carbonylation or simply excess phosphine for alkene and alkyne insertions. In principle, the chain extension process can be repeated indefinitely to produce polymers by Ziegler-Natta polymerization, which is described in Chapter 52. [Pg.1317]

Theoretically, it is possible for the process of olefin coordination and insertion to continue as in Ziegler-Natta polymerization (Chapter 52) but with palladium the metal is expelled from the molecule by a p-hydride elimination reaction and the product is an alkene. For the whole process to be catalytic, a palladium(O) complex must be regenerated from the palladium(ll) product of P-hydride elimination. This occurs in the presence of base which removes HX from the palladium(II) species. [Pg.1320]

One such process is the Cossee-Arlman mechanism,proposed for the Ziegler-Natta polymerization of alkenes (also discussed in Section 14-4-1). According to this mechanism, a polymer chain can grow as a consequence of repeated 1,2 insertions into a vacant coordination site, as follows ... [Pg.533]

The Ziegler-Natta polymerization of ethylene can be adapted to make molecules of only modest size (C6--C20) and containing certain functional groups. If, for example, the mctal-alkyls initially obtained are heated (in the presence of ethylene and a nickel catalyst), the hydrocarbon groups are displaced as straight-chain 1-alkenes of even carbon number. Large quantities of such alkenes in the C12-C20 range are... [Pg.1041]


See other pages where Alkene Ziegler-Natta polymerization is mentioned: [Pg.610]    [Pg.359]    [Pg.345]    [Pg.187]    [Pg.237]    [Pg.118]    [Pg.577]    [Pg.5]    [Pg.5]    [Pg.178]    [Pg.139]    [Pg.3204]    [Pg.1219]    [Pg.978]    [Pg.565]    [Pg.565]    [Pg.1152]   
See also in sourсe #XX -- [ Pg.1270 , Pg.1271 , Pg.1272 , Pg.1273 ]




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