Ring-opening polymerization polymers made

Since it was shown that free radical ring-opening polymerization (2) made it possible to introduce functional groups, such as esters C3j, carbonates (4), thioesters (5), and amides (6), into the backbone of an addition polymer, it was reasoned that simple hydrolysis would produce the desired oligomers that could be terminated with various combinations of hydroxyl, amino, thiol, and carboxylic acid groups. 

Braided Synthetic Absorbable Sutures. Suture manufacturers have searched for many years to find a synthetic alternative to surgical gut. The first successful attempt to make a synthetic absorbable suture was the invention of polylactic acid [26023-30-3] suture (15). The polymer was made by the ring-opening polymerization of L-lactide [95-96-5] (1), the cycUc dimer of L-lactic acid. 

Nylon 66 is a condensation polymer made from adipic acid and iiexamethylenediamine. Nylon 6 is made by ring-opening polymerization of caprolactam. 

This indicates the possibility of making addition polymers biodegradable by the introduction of ester linkages in to the backbone. Since the free radical ring-opening polymerization of cyclic ketene acetals, such as 2-methylene-1,3-dioxepane (1, Scheme I), made possible the introduction of ester groups into the backbone of addition polymers, this appeared to be an attractive method for the synthesis of biodegradable addition polymers. 

This polymer is obviously totally inorganic, and can be made directly by the ring-opening polymerization of rhombic sulfur, which consists of eight-membered sulfur rings. 

In the second chapter, we try to emphasize the possibilities of producing tailor-made polymers with predicted properties. By using different types of initiators and catalysts, ring-opening polymerization of lactones and lactides provides macromolecules with advanced molecular architecture - a careful selection of appropriate conditions is crucial. The purpose of this chapter is also to describe the mechanisms and typical kinetic features. 

Spiro orthoesters (92, R = Me, Ph, and H) show typical equilibrium polymerization behavior at or below ambient temperature. [92] The poly(cyclic orthoester)s derived from 92 depolymerize to the monomers, although they have sufficient strains to be able to undergo ring-opening polymerization. The polymerization enthalpies and entropies for these three monomers were evaluated from the temperature dependence of equilibrium monomer concentrations (Table 5). The enthalpy became less negative as the size of the substituent at the 2-position in 92 was increased H < Me < Ph. This behavior can be explained in terms of the polymer state being made less stable by steric repulsion between the bulky substituents and/or between the substituent and the polymer main chain. The entropy also changed in a similar manner with the size of the substituents. 

In the literature, linear polymers are referred to as poly(iminoethylene), and branched polymers as poly(ethylenimine), since the latter derive from the ring-opening polymerization of ethylenimine. In this review, both polymers will be referred to as PEI. Mention will be made, however, to their structure whenever opportune. 

Nylon 6,6 and nylon 6 are polyamides. These polymers are used in carpets, in hosiery, and in certain cases as engineering plastics. Nylon 6,6 8.19, is the condensation product between adipic acid and 1,6-diamino hexane. Nylon 6 8.20 is made from caprolactam by ring-opening polymerization. 

The use of dicarbodiimides as monomers in polyaddition reactions have not as yet found wide utility. However, polymers containing carbodiimide groups are known, and further nucleophilic reactions of these polymers with numerous substrates are reported. Carbodiimides, generated in situ from isocyanates are used as catalyst in the formation of polyamides from diisocyanates and dicarboxylic acids. Also, homoleptic lanthanide amidinates, made from carbodiimides, exhibit high catalytic activity for the ring opening polymerization of e-caprolactone at room temperature. ... 

Polyoxymethylene polymers, POM, commonly known as polyacetals or Acetal resins are linear thermoplastic polymers containing predominantly the -CH -O- repeat unit in their backbone. There are two types of acetal resins available commercially (1) homopolymers made by the polymerization of formaldehyde, followed by endcapping, (2) copolymers derived from the ring opening polymerization of trioxane (a cyclic trimer of formaldehyde), and a small amount of a comonomer such as ethylene oxide. Acetal resins are... 

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