Poly definition

A plasticizer is a substance the addition of which to another material makes that material softer and more flexible. This broad definition encompasses the use of water to plasticize clay for the production of pottery, and oils to plasticize pitch for caulking boats. A more precise definition of plasticizers is that they are materials which, when added to a polymer, cause an increase in the flexibiUty and workabiUty, brought about by a decrease in the glass-transition temperature, T, of the polymer. The most widely plasticized polymer is poly(vinyl chloride) (PVC) due to its excellent plasticizer compatibility characteristics, and the development of plasticizers closely follows the development of this commodity polymer. However, plasticizers have also been used and remain in use with other polymer types. 

Polyanilines. Initial preparations of polyaniline (PANI) led to insoluble materials that were difficult to characterize. Use of model compounds and polymers (124,125) allowed for definitive stmctural analysis. Poly( phenylene amineimine) (PPAI) was synthesized directiy to demonstrate that PANI is purely para-linked (126). The synthesis was designed so as to allow linkage through the nitrogen atoms only (eq. 9). Comparison of the properties of PPAI and PANI showed PPAI to be an excellent model both stmcturaHy and electronically. 

In reactions at the sulfur atom of a sulfinate ion to form a sulfone, of a sulfoxide to form R3S+—0, or of bisulfite ion to form a sulfonic acid, the fractionally positive sulfur becomes more positively charged in the poly-ionic transition states. Definitive experimental evidence... 

An interesting aspect of the benzofuran cationic polymerization was uncovered by Natta, Farina, Peraldo and Bressan who reported in 196160,61 that an asymmetric synthesis of an optically active poly(benzofuran) could be achieved by using AlCl2Et coupled with (-)j3-phenylalanine, (+)camphorsulphonic acid or with (-)brucine. The optical activity was definitely due to the asymmetric carbon atoms in the polymer chain, indicating that at least some of the polymer s macromolecules possessed a di-isotactic structure, v/ z.62 ... 

These compds may be modified by monocar-boxy lie acids or poly hydroxy alcohols. This definition includes the polycarbonates (qv), which are a well-defined segment of the general class of polyesters. Unsaturated polyesters, which are produced when any of the reactants contain non-aromatic unsaturation, can be cross-linked or copolymerized with an un-saturated copolymerizable monomer. The formulas and properties of the class polyester are as varied and extensive as the reactants themselves. For specific information on the various sub-classes and sub-sub classes, the following refs should be consulted 9, 10, II, 16a, 17,18,... 

In this review the definition of orientation and orientation functions or orientation averages will be considered in detail. This will be followed by a comprehensive account of the information which can be obtained by three spectroscopic techniques, infra-red and Raman spectroscopy and broad line nuclear magnetic resonance. The use of polarized fluorescence will not be discussed here, but is the subject of a contemporary review article by the author and J. H. Nobbs 1. The present review will be completed by consideration of the information which has been obtained on the development of molecular orientation in polyethylene terephthalate and poly(tetramethylene terephthalate) where there are also clearly defined changes in the conformation of the molecule. In this paper, particular attention will be given to the characterization of biaxially oriented films. Previous reviews of this subject have been given by the author and his colleagues, but have been concerned with discussion of results for uniaxially oriented systems only2,3). 

This concept covers most situations in the theory of AB cements. Cements based on aqueous solutions of phosphoric acid and poly(acrylic acid), and non-aqueous cements based on eugenol, alike fall within this definition. However, the theory does not, unfortunately, recognize salt formation as a criterion of an acid-base reaction, and the matrices of AB cements are conveniently described as salts. It is also uncertain whether it covers the metal oxide/metal halide or sulphate cements. Bare cations are not recognized as acids in the Bronsted-Lowry theory, but hydrated... 

In transition metal-catalyzed domino reactions, more than one catalyst is often employed. In Tietze s definition and the classification of domino reactions, no distinction has been made between transformations where only one or more transition metal catalyst is used for the different steps, provided that they take place in a chronologically distinct order. Poli and coworkers [13] differentiated between these processes by calling them pure-domino reactions (which consisted of a single catalytic cycle driven by a single catalytic system) or pseudo-domino reactions . The latter type was subdivided into ... 

Figure 8.3. LORENTZ-polarization corrected WAXS curve of poly(3-dodecylthiophene) before and after background subtraction (from PROSA et al. [109]). The authors define q in the way that is identical to the definition of s in this book...

The regulations prescribe the energy values to be used as in Table 3. There are agreed values for some other materials. The synthetic dextrose polymer poly dextrose is accepted to be only 1 kcal g 1 (or 4 kJ g 1) even though it would otherwise fall within the definition of a carbohydrate. The accepted value for gum acacia, a polysaccharide obtained from trees of the species Acacia Senegal and closely related species, is 2 kcal g 1 (or 8 kJ g-1). 

Fujiki also reported end-chain chiral functionalization in (.S )-2-methy I butyl-terminated poly( -hexyl-2-methylpro-pylsilylene), 114, and found a weak, though definite, induced PSS (gabs — 1 x 10 s) of the opposite sign to the PSS induced when the unichiral groups were incorporated in the side chains.204 323... 

Table IV summarizes the results for the resist screening studies at SSRL. The resist candidates generally exhibited good sensitivity, Dg 5 < 50 mJ/cm2, and contrast, 7 = 1.5. Definitive conclusions regarding the effect of structure on sensitivity are made difficult by the fact that polymer molecular weight and poly-dispersity varied considerably from sample to sample and, since we found a very strong dependence of Dg 5 on these parameters, specific structural effects are obscured. Several generalizations can be made, however.

General Comment. The foregoing examples clearly show that poly(vinyl alcohol) can be modified readily and that some of these derivatives have potential (and/or actual) biological activity. This survey is definitely not encyclopedic in scope but rather illustrative. No doubt many more examples of potentially biologically active poly(vinyl alcohol) derivatives will be developed in the future and it is entirely possible that some of these may become of value in chemotherapy and other areas where biologically active polymers are now being studied. 

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