Methyl polymerized

Reduction of the ester fimction or addition of Grignard reagents led to supported-amino alcohols 178-181 (Scheme 78). The nitrogen atom of these polymers was then methylated to afford the iV-methylaled polymeric aminoalcohols 182-185. 

Partially methylated sugars may be prepared from the corresponding methylated polymerizing substances. Thus, methoxyacetaldehyde, prepared by chromic acid oxidation of methoxyethanol, polymerizes in the presence of potassium carbonate to 2,4-di-O-methylaldotetrose 174). 

CHi=CMeCOOH. Colourless prisms m.p. 15-16 C, b.p. 160-5 C. Manufactured by treating propanone cyanohydrin with dilute sulphuric acid. Polymerizes when distilled or when heated with hydrochloric acid under pressure, see acrylic acid polymers. Used in the preparation of synthetic acrylate resins the methyl and ethyl esters form important glass-like polymers. 

CHjlCH COOH. Colourless liquid having an odour resembling that of ethanoic acid m.p. 13 C, b.p. I4I°C. Prepared by oxidizing propenal with moist AgO or treating -hy-droxypropionitrile with sulphuric acid. Slowly converted to a resin at ordinary temperatures. Important glass-like resins are now manufactured from methyl acrylate, see acrylic resins. Propenoic acid itself can also be polymerized to important polymers - see acrylic acid polymers. 

Figure 14 5 outlines a mechanism for ethylene polymerization m the presence of Cp2ZrCl2 Step 1 describes the purpose of the MAO promoter which is to transfer a methyl group to the metallocene to convert it to its catalytically active form This methyl group will be incorporated into the growing polymer chain—indeed it will be the end from which the rest of the chain grows... 

Hydroxy-2-methylpropanenitrile is then reacted with methanol (or other alcohol) to yield methacrylate ester. Free-radical polymerization is initiated by peroxide or azo catalysts and produce poly(methyl methacrylate) resins having the following formula ... 

Poly (methyl Acrylate). The monomer used for preparing poly(methyl acrylate) is produced by the oxidation of propylene. The resin is made by free-radical polymerization initiated by peroxide or azo catalysts and has the following formula ... 

Poly(methylpentene) is obtained by a Ziegler-type catalytic polymerization of 4-methyl-1-pentene. 

Figure 6.2 Acceleration of the polymerization rate for methyl methacrylate at the concentrations shown in benzene at 50 C. [Reprinted from G. V. Schulz and G. Haborth, Makromol. Chem. 1 106 (1948).]...

Figure 6.3 shows some data which constitute a test of Eq. (6.26). In Fig. 6.3a, Rp and [M] are plotted on a log-log scale for a constant level of redox initiator. The slope of this line, which indicates the order of the polymerization with respect to monomer, is unity, showing that the polymerization of methyl methacrylate is first order in monomer. Figure 6.3b is a similar plot of the initial rate of polymerization—which essentially maintains the monomer at constant con-centration—versus initiator concentration for several different monomer-initiator combinations. Each of the lines has a slope of indicating a half-order dependence on [I] as predicted by Eq. (6.26).

In cationic polymerization the active species is the ion which is formed by the addition of a proton from the initiator system to a monomer. For vinyl monomers the type of substituents which promote this type of polymerization are those which are electron supplying, like alkyl, 1,1-dialkyl, aryl, and alkoxy. Isobutylene and a-methyl styrene are examples of monomers which have been polymerized via cationic intermediates. 

AIBN was synthesized using C-labeled reagents and the tagged compound was used to initiate polymerization of methyl methacrylate and styrene. 

Arnett + initiated the polymerization of methyl methacrylate in benzene at ... 

Figure 7.8 Mole fractions styrene (Mj) and methyl methacrylate (M2) in feedstock (f) and copolymers (F) as a function of the extent of polymerization. Average copolymer compositions are also shown. [From V. E. Meyer and R. K. S. Chan, Polym. Prepr. 8 209(1967), used with permission.]...

Fox and Schneckof carried out the free-radical polymerization of methyl methacrylate between -40 and 250 C. By analysis of the a-methyl peaks in the NMR spectra of the products, they determined the following values of a, the probability of an isotactic placement in the products prepared at the different temperatures ... 

Under acidic conditions, furfuryl alcohol polymerizes to black polymers, which eventually become crosslinked and insoluble in the reaction medium. The reaction can be very violent and extreme care must be taken when furfuryl alcohol is mixed with any strong Lewis acid or Brn nstad acid. Copolymer resins are formed with phenoHc compounds, formaldehyde and/or other aldehydes. In dilute aqueous acid, the predominant reaction is a ring opening hydrolysis to form levulinic acid [123-76-2] (52). In acidic alcohoHc media, levulinic esters are formed. The mechanism for this unusual reaction in which the hydroxymethyl group of furfuryl alcohol is converted to the terminal methyl group of levulinic acid has recendy been elucidated (53). 

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