Poly linear polymer synthesis

Linear Polymer with Chiral Units 9.4.2.1 Synthesis of Poly (thiophene) 11724a... 

Linear phosphonitrilic chlorides (LPNCs), silicone fluids and, 22 573 Linear photodiode arrays, 19 153 Linear polyesters, 14 116 Linear polyethylene fibers, 20 398 Linear polyimides, synthesis of, 20 273 Linear polymers, 20 391 25 455 high molecular weight, 23 733 zero-shear viscosity of, 19 839 Linear poly(thioarylene)s, 23 705 Linear PPS, 23 704. See also... 

Diffiuex investigated a synthesis of cyclic poly(vinyl ether) using cationic polymerization [26,28]. The reaction process is depicted in Fig. 9. They studied on the living cationic polymerization of 2-chloroethyl vinyl ether (CEVE) initiated with the HI adduct of 4-(vinylbenzyloxy)butyl vinyl ether prepared by reacting chloromethyl styrene with sodium salt of 4-hydroxy-butyl vinyl ether in THF at 80 °C. By the cationic polymerization of CEVE, o /o-hetcrofunclional linear polymer precursor of cyclic poly(CEVE) was produced. The MWDs of the polymers were unimodal and very narrow (< 1.2),... 

Cross-linked resins of polyamidoamine structure can be prepared in the same way as the linear polymers by partly substituting a, m-diaminoalkanes for the same quantity of difunctional aminic monomers in the polymerization process. According to the general scheme of poly(amido-amine)synthesis, bis(primary amine)s, having four mobile hydrogens, act as tetrafunctional monomers 47). 

A benzyl bromide-type initiator (MI-27) was utilized for the copper-catalyzed synthesis of 3-armed poly(acrylate)s with mesogen units as side-chain groups.324 The effect of molecular architecture on the thermotropic behavior was compared with the corresponding linear polymers in both living and conventional polymerizations. 

The synthesis and characterization of four distinct families of poly (ortho esters) are described and designated as poly (ortho esters) I, II, III and IV. Poly (ortho ester) I is prepared by the transesterification of diethoxytetrahydrofuran with diols. Poly (ortho ester) II is prepared by the condensation of 3,9-bis (ethylidene 2,4,8,10-tetraoxaspiro [5, 5] undecane) with diols to produce a linear polymer or with a triol to produce a crosslinked polymer. Poly (ortho ester) III is prepared by the condensation of a flexible triol with and alkyl orthoacetate to produce ointment-like materials. Poly (ortho ester) IV is prepared by the condensation of a rigid triol with and alkyl orthoacetate to produce solid materials. The detailed mechanism of hydrolysis of these polymers has been determined and drug release data for a number of therapeutic agents are presented. 

For organic encapsulation we have used the electrochemical synthesis of poly(oxy-phenylene) as originally presented by Mengoli et al. It is done by the electrochemical oxidation of 2-allylphenol in water/methanol/butylcellosolve mixture to yield poly(oxyphenyl-ene). This electrooxidation is done in the presence of allylamine in order to minimize the competing passivation of the substrate and to crosslink the linear polymer during the curing step. 

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