High polymer reaction

Thus, the second approach to the synthesis of poly(organophosphazenes) involves the introduction of the organic (or organometallic) side groups at the cyclic trimer level, followed by ring-opening polymerization of the substituted cyclic trimer to the high polymer (reaction (ll)).23... 

Dienes. The dienes present a particularly challenging case since both stereoisomerism and geometric isomerism can be observed in the products (the dienes are not only polyfunctional but also permit different tacticities). For butadiene, the following possibilities exist trans-1,4 cis-1,4 atactic 1,2 isotactic 1,2 syndiotactic 1,2 cyclic oligomers and cyclic high polymers (Reaction 16). 

W. A. Bishop, High Temperature Infrared Cells for Studies of Solid High Polymer Reactions, Anal. Chem. 33, 456, 1961. 

Polyester resins can also be rapidly formed by the reaction of propylene oxide (5) with phthaUc and maleic anhydride. The reaction is initiated with a small fraction of glycol initiator containing a basic catalyst such as lithium carbonate. Molecular weight development is controlled by the concentration of initiator, and the highly exothermic reaction proceeds without the evolution of any condensate water. Although this technique provides many process benefits, the low extent of maleate isomerization achieved during the rapid formation of the polymer limits the reactivity and ultimate performance of these resins. 

Plastics are made by a chemical reaction in which monomers add (with nothing left over) or condense (with FljO left over) to give a high polymer. 

The highly exothermic reaction has already been mentioned. It is particularly important to realise that at the elevated temperatures employed other reactions can occur leading to the formation of hydrogen, methane and graphite. These reactions are also exothermic and it is not at all difficult for the reaction to get out of hand. It is necessary to select conditions favourable to polymer formation and which allow a controlled reaction. 

It has not been found possible to prepare high polymers from a-methylstyrene by free-radical methods and ionic catalysts are used. The reaction may be carried out at about -60°C in solution. 

The opening of the caprolactam ring for nylon 6 involves an equilibrium reaction which is easily catalysed by water. In the case of nylon 12 from dodecanelactam, higher temperatures, i.e. above 260°C, are necessary for opening the ring structures but since in this case the condensation is not an equilibrium reaction the process will yield almost 100% of high polymer. ... 

Polyethylene is the simplest of so-called high polymers. The reaction for low density polyethylene (LDPE) follows the classical free radical polymerization steps of initiator decomposition, initiation, propagation, and termination. The reaction is... 

In the polymerization of phenyl acetylene [27] by tungsten and mo]ybdenum hexcarbonyls, high-polymer yields were obtained in CCI4 solvent. The following reaction scheme was proposed, which is different from that reported by Bamford and coworkers [17-20] ... 

A systematic study of this class of compounds did not start until twenty years later and led to the preparation of a series of M3Q7X4 (M = Mo, W Q = S, Se and X = C1, Br) inorganic polymers by high-temperature reactions (ca. 350 °C) of the elements in a sealed tube [10-14]. The interest on these cluster phases was mainly motivated by their excellent role as synthons for the preparation of molecular M3Q7 and M3Q4 cluster complexes, as will be presented in this section. 

The statistical approach has since assumed a dominant role in the treatment of the constitution, reactions, and physical properties of polymeric substances. The complexities of high polymers are far too great for a direct mechanistic deduction of properties from the detailed structures of the constituent molecules even the constitution of... 

Work on phosphazene high polymers continues to attract increased interest. Advances in the study of the ring-opening polymerization, and physical characterization in the solid state, of the materials produced by these reactions have been reported. 

The discovery that soluble high molecular weight polysilanes may be prepared by the reductive coupling of dichlorodialkylsilanes by alkali metals (1,2) has led to considerable work on the properties of this interesting class of polymers (3,4,5). The preparation of the polymers leaves much to be desired as frequently the high polymer is only a minor product. Mechanistic studies of the reaction with a view to improving the relevant yields have been few (6). The major ones by Zeigler (7,8,9) showed that a silylene diradical was not involved in the reaction, and stressed the importance of polymer solvent interactions. 

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