Isomer of polymers

In solid, the molecules of trans isomers pack more closely and crystallize more readily than those of cis isomers. This is reflected in the fact that the melting point of fumaric acid is about 160°C higher than that of of maleic acid. Similarly, the differences in the properties of cis and trans isomers of polymers are also significant, as shown below with the example of poly(isoprene). 

Table 6.1 Thermal behavior of ordered and random constitutional isomers of polymer P5 (data from [3])...

When a synthetic fiber is stretched or drawn, the molecules in most cases will orient themselves in crystalline areas parallel to the fiber axis, although crystalline areas in some chain-folded polymers such as polypropylene can be aligned vertical to the fiber axis. The degree of crystallinity will be affected by the total forees available for chain interaction, the distance between parallel chains, and the similarity and uniformity of adjacent chains. The structure and arrangement of individual polymer chains also affects the morphology of the fiber. Also, configurations or optical isomers of polymers can have very different phys-ieal and chemical properties. 

The allyl bromides formed by method (A) contain 25% of the undesired (Z)-isomer. The selectivity of the palladium-catalyzed amination can be steered by the application of polymer-bound systems (see section 2.6.3 B. M. Trost, 1978),... 

Although the conditions of the polymerization reaction may be chosen to optimize the formation of one specific isomer, it is typical in these systems to have at least some contribution of all possible isomers in the polymeric product, except in the case of polymers of biological origin, like natural rubber and gutta-percha. 

The polymerization of j3-carboxymethyl caprolactam has been observed to consist of initial isomerization via a second-order kinetic process followed by condensation of the isomer to polymer ... 

Other minor raw materials are used for specific needs. Eumaric acid [110-17-8] the geometric isomer of maleic acid, is selected to maximize thermal or corrosion performance and is the sole acid esterified with bisphenol A diol derivatives to obtain optimum polymer performance. CycloaUphatics such as hydrogenated bisphenol A (HBPA) and cyclohexanedimethanol (CHDM) are used in selective formulations for electrical apphcations. TetrahydrophthaUc anhydride [85-43-8] (THPA) can be used to improve resiUence and impart useful air-drying properties to polyester resins intended for coating or lining apphcations. 

The steric effects in isocyanates are best demonstrated by the formation of flexible foams from TDI. In the 2,4-isomer (4), the initial reaction occurs at the nonhindered isocyanate group in the 4-position. The unsymmetrically substituted ureas formed in the subsequent reaction with water are more soluble in the developing polymer matrix. Low density flexible foams are not readily produced from MDI or PMDI enrichment of PMDI with the 2,4 -isomer of MDI (5) affords a steric environment similar to the one in TDI, which allows the production of low density flexible foams that have good physical properties. The use of high performance polyols based on a copolymer polyol allows production of high resiHency (HR) slabstock foam from either TDI or MDI (2). 

Compounds whose molecular compositions are multiples of a simple stoichiometry are polymers, stricdy, only if they are formed by repetition of the simplest unit. However, the name polymerization isomerism is applied rather loosely to cases where the same stoichiometry is retained but where the molecular arrangements are different. The stoichiometry PtCl2(NH3)2 applies to the 3 known compounds, [Pt(NH3)4][PtCU], [Pt(NH3)4][PtCl3(NH3)]2, and [PtCl(NH3)3]2[PtCl4] (in addition to the cis and trans isomers of monomeric [PtCl2(NH3)2]). There are actually 7 known compounds with the stoichiometry Co(NH3)3(N02)3. Again it is clear that considerable differences are to be expected in the chemical properties and in physical properties such as conductivity. 

As noted in the Chapter 7 Focus On, rubber is a naturally occurring polymer of isoprene, or 2-methyl-l,3-butadiene. The double bonds of rubber have Z stereochemistry, but gutta-percha, the E isomer of rubber, also occurs naturally. Harder and more brittle than rubber, gutta-percha has a variety of minor applications, including occasional use as the covering on golf balls. 

One practical example of demixing that might be attributed to a difference in crystallizability is the incompatibility in blends of polymers with different stereochemical compositions. The stereochemical isomers contain both chemical and geometrical similarities, but differ in the tendency of close packing. In this case, both the mixing energy B and the additional mixing entropy due to structural asymmetry between two kinds of monomers are small. However, the stereochemical differences between two polymers will result in a difference in the value of Ep. Under this consideration, most experimental observations on the compatibility of polymer blends with different stereochemical compositions [89-99] are tractable. For more details, we refer the reader to Ref. [86]. 

Campo et al. (1999) synthesized the ortho-isomers of PCPP and PCPH, poly[l,3-bis(o-carboxyphenoxy)propane] (Po-CPP) and poly[l,6-bis( o-carboxyphenoxy)hexane] (Po-CPH), in an attempt to improve the solubility and processability of these two polymers. Solubility was improved... 

The 1,3-dipolar cycloaddition of nitrones to vinyl ethers is accelerated by Ti(IV) species. The efficiency of the catalyst depends on its complexation capacity. The use of Ti( PrO)2Cl2 favors the formation of trans cycloadducts, presumably, via an endo bidentate complex, in which the metal atom is simultaneously coordinated to the vinyl ether and to the cyclic nitrone or to the Z-isomer of the acyclic nitrones (800a). Highly diastereo- and enantioselective 1,3-dipolar cycloaddition reactions of nitrones with alkenes, catalyzed by chiral polybi-naphtyl Lewis acids, have been developed. Isoxazolidines with up to 99% ee were obtained. The chiral polymer ligand influences the stereoselectivity to the same extent as its monomeric version, but has the advantage of easy recovery and reuse (800b). 

Examples of ditactic polydienes are provided by a class of crystalline polymers derived from the alkyl-esters of the trans-trans isomer of sorbic acid.101,102 For example trans-poly (methyl sorbate) (-CH(CH3)-CH =... 

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