Poly , polymeric

PPA = polyphosphoric acid al = alkylation ac = acylation chlor = chlorination iso = isomerization halo = halogenation cycl = cyclization poly = polymerization for = formylation dehydr = dehydration nitr - nitration general = active in most Friedel-Crafts reactions deal = dealkylation rearr = rearrangement. 

CHR) , formed, e g. from the reaction of diazomethane and alcohols or hydroxylamine derivatives in the presence of boron compounds or with metal compounds. Poly-methylene is formally the same as polyethene and the properties of the various polymers depend upon the degree of polymerization and the stereochemistry. 

Several studies have demonstrated the successful incoriDoration of [60]fullerene into polymeric stmctures by following two general concepts (i) in-chain addition, so called pearl necklace type polymers or (ii) on-chain addition pendant polymers. Pendant copolymers emerge predominantly from the controlled mono- and multiple functionalization of the fullerene core with different amine-, azide-, ethylene propylene terjDolymer, polystyrene, poly(oxyethylene) and poly(oxypropylene) precursors [63,64,65,66,62 and 66]. On the other hand, (-CggPd-) polymers of the pearl necklace type were fonned via the periodic linkage of [60]fullerene and Pd monomer units after their initial reaction with thep-xy y ene diradical [69,70 and 71]. 

The second category of polymerization reactions does not involve a chain reaction and is divided into two groups poly addition and poly condensation [4]. In botli reactions, tire growth of a polymer chains proceeds by reactions between molecules of all degrees of polymerization. In polycondensations a low-molecular-weight product L is eliminated, while polyadditions occur witliout elimination ... 

Ghassemieli, E. and Nassehi, V., 2001a. Stiffness analysis of polymeric composites using the finite element method. Adv. Poly. Tech. 20, 42-57. 

Diisocyanobenzene (130) undergoes living polymerization to form the poly(quinoxaline-2,3-diyl)s 131, and the optically active helical polyfquinoxa-line-2,3-diyl) 132 is prepared from 131[123]. 

ETHYLENE We discussed ethylene production in an earlier boxed essay (Section 5 1) where it was pointed out that the output of the U S petrochemi cal industry exceeds 5 x 10 ° Ib/year Approximately 90% of this material is used for the preparation of four compounds (polyethylene ethylene oxide vinyl chloride and styrene) with polymerization to poly ethylene accounting for half the total Both vinyl chloride and styrene are polymerized to give poly(vinyl chloride) and polystyrene respectively (see Table 6 5) Ethylene oxide is a starting material for the preparation of ethylene glycol for use as an an tifreeze in automobile radiators and in the produc tion of polyester fibers (see the boxed essay Condensation Polymers Polyamides and Polyesters in Chapter 20)... 

As the demand for rubber increased so did the chemical industry s efforts to prepare a synthetic sub stitute One of the first elastomers (a synthetic poly mer that possesses elasticity) to find a commercial niche was neoprene discovered by chemists at Du Pont in 1931 Neoprene is produced by free radical polymerization of 2 chloro 1 3 butadiene and has the greatest variety of applications of any elastomer Some uses include electrical insulation conveyer belts hoses and weather balloons... 

Coordination polymerization of isoprene using Ziegler-Natta catalyst systems (Section 6 21) gives a material similar in properties to natural rubber as does polymerization of 1 3 butadiene Poly(1 3 buta diene) is produced in about two thirds the quantity of SBR each year It too finds its principal use in tires... 

Polymerization of styrene is carried out under free radical conditions often with benzoyl peroxide as the initiator Figure 1111 illustrates a step m the growth of a poly styrene chain by a mechanism analogous to that of the polymerization of ethylene (Sec tion 6 21)... 

Poly(vinyl alcohol) is a useful water soluble polymer It cannot be prepared directly from vinyl alcohol because of the rapidity with which vinyl alcohol (H2C=CHOH) isomenzes to acetaldehyde Vinyl acetate however does not rearrange and can be polymerized to poly(vinyl acetate) How could you make use of this fact to prepare poly(vinyl alcohol)" ... 

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 ... 

Polylacrylic Acid) and Poly(methacrylic Acid). Glacial acrylic acid and glacial meth-acrylic acid can be polymerized to produce water-soluble polymers having the following structures ... 

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

Commonly used isocyanates are toluene dhsocyanate, methylene diphenyl isocyanate, and polymeric isocyanates. Polyols used are macroglycols based on either polyester or polyether. The former [poly(ethylene phthalate) or poly(ethylene 1,6-hexanedioate)] have hydroxyl groups that are free to react with the isocyanate. Most flexible foam is made from 80/20 toluene dhsocyanate (which refers to the ratio of 2,4-toluene dhsocyanate to 2,6-toluene dhsocyanate). High-resilience foam contains about 80% 80/20 toluene dhsocyanate and 20% poly(methylene diphenyl isocyanate), while semi-flexible foam is almost always 100% poly(methylene diphenyl isocyanate). Much of the latter reacts by trimerization to form isocyanurate rings. 

If a polymer is formed from a single monomer, as in addition and ringopening polymerizations, it is named by attaching the prefix poly to the name... 

The ethylene glycol liberated by reaction (5.L) is removed by lowering the pressure or purging with an inert gas. Because the ethylene glycol produced by reaction (5.L) is removed, proper stoichiometry is assured by proceeding via the intermediate, bis(2-hydroxyethyl) terephthalate otherwise the excess glycol used initially would have a deleterious effect on the degree of polymerization. Poly(ethylene terephthalate) is more familiar by some of its trade names Mylar as a film and Dacron, Kodel, or Terylene as fibers it is also known by the acronym PET. 

The polymer described in the last problem is commercially called poly (phenylene oxide), which is not a proper name for a molecule with this structure. Propose a more correct name. Use the results of the last problem to criticize or defend the following proposition The experimental data for dimer polymerization can be understood if it is assumed that one molecule of water and one molecule of monomer may split out in the condensation step. Steps involving incorporation of the monomer itself (with only water split out) also occur. 

It has been observedt that poly(1,1-dimethyl propane) is the product when 3-methylbutene-l is polymerized with AICI3 in ethyl chloride at -130°C. Write structural formulas for the expected repeat units and those observed and propose an explanation. 

Poly(acrylic acid) and Poly(methacrylic acid). Poly(acryHc acid) (8) (PAA) may be prepared by polymerization of the monomer with conventional free-radical initiators using the monomer either undiluted (36) (with cross-linker for superadsorber appHcations) or in aqueous solution. Photochemical polymerization (sensitized by benzoin) of methyl acrylate in ethanol solution at —78° C provides a syndiotactic form (37) that can be hydrolyzed to syndiotactic PAA. From academic studies, alkaline hydrolysis of the methyl ester requires a lower time than acid hydrolysis of the polymeric ester, and can lead to oxidative degradation of the polymer (38). Po1y(meth acrylic acid) (PMAA) (9) is prepared only by the direct polymerization of the acid monomer it is not readily obtained by the hydrolysis of methyl methacrylate. 

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