Ziegler-Natta chain-growth

Alternatively, the intermediate acetaldehyde (qv) for this process was obtained from ethylene by the Wacker process (9). A small amount of -butyl alcohol is produced in the United States by the Ziegler-Natta chain growth reaction from ethylene [74-85-1] (10). 

Ziegler-Natta chain-growth polymerization involves the formation of an alkyl-transition metal compound and then the repeated insertion of alkene monomers into the transition metal-to-carbon bond to yield a saturated polymer chain. 

Ziegler-Natta chain-growth polymerization of ethylene and substituted ethylenes (Section 16.5B)... 

Titanium-Mediated (Ziegler-Natta) Chain-Growth Polymerization of Ethylene and Substituted Ethylenes (Section 29.6B)... 

Assume as a model for a Ziegler-Natta system the diffusion of monomer to a site of catalytic activity—presumably one of a number of sites on a solid particle—where it is inserted into a growing polymer chain. For the bulk polymerization of a monomer such as 4-methylpentene-l where polymer is insoluble in monomer, the solid catalyst particle becomes the center of an expanding sphere of precipitated polymer chain (s) growing from the inside. On this molecular level, the rate of chain growth will be directly proportional to the monomer activity at the individual sites. At equilibrium the monomer activity at each site encapsulated in precipitated polymer will equal that of the surrounding bulk monomer, [Mo]. Under nonequilibrium conditions, where the rate of diffusion of monomer from the bulk monomer thru the precipitated polymer to the polymerization site becomes comparable to the rate of polymerization at that site, the localized activity will be lower, and the rate of polymerization will be correspondingly lower. 

Many examples of such eliminations have now been seen for the f-block and for d metals. This type of /3-aIkyl elimination is recognized as an important chain transfer step in Ziegler-Natta and metallocene polymerization catalysis. When it occurs the polymer chain terminates in a C=C bond (equation 2) and in certain cases the aUcene chain end can undergo reinsertion and get back into the polymer growth... 

Using Ziegler-Natta catalysts, the termination of the polymer chain growth can proceed with the participation of a cocatalyst, a monomer, or hydrogen or via a P-hydride shift ... 

Despite passage of more than 57 years since the basic discoveries, the mechanism of Ziegler-Natta polymerization is still not fully understood. As in all chain-growth polymerizations (12), the basic steps are initiation, propagation and termination (chain transfer). 

Additionally, if the initiation reaction is more rapid an the chain propagation, a very narrow molecular weight distribution, MJM = 1 (Poisson distribution), is obtained. Typically living character is shown by the anionic polymerization of butadiene and isoprene with the lithium alkyls [77, 78], but it has been found also in butadiene polymerization with allylneodymium compounds [49] and Ziegler-Natta catalysts containing titanium iodide [77]. On the other hand, the chain growth can be terminated by a chain transfer reaction with the monomer via /0-hydride elimination, as has already been mentioned above for the allylcobalt complex-catalyzed 1,2-polymerization of butadiene. 

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