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Chemical synthesis polymerizations

The synthesis involves the nickel-catalyzed coupling of the mono-Grignard reagent derived from 3-alkyl-2,5-diiodothiophene (82,83). Also in that year, transition-metal hahdes, ie, FeCl, MoCl, and RuCl, were used for the chemical oxidative polymerization of 3-substituted thiophenes (84). Substantial decreases in conductivity were noted when branched side chains were present in the polymer stmcture (85). [Pg.37]

Some six hundred structures of naturally occurring carbogenic molecules appe on the pages which follow, together with the name of each compound and references to the original literature of successful chemical synthesis. Thus, Part Three of this book is effectively a key to the literature of chemical synthesis as applied to the complex molecules of nature. The survey does not include oligomeric or polymeric structures, such as peptides, proteins, carbohydrates and polynucleotides, which fall outside the scope of this book because they can be assembled by repetitive procedures. [Pg.359]

Ring-opening polymerization has played an important role in systematic approaches to the chemical synthesis of polysaccharides and the clarification of their biomedically interesting characteristics in relation to their own molecular structures. The early... [Pg.48]

Acryl amide is an important bulk chemical used in coagulators, soil conditioners and stock additives. The chemical synthesis has several drawbacks because the rate of acryl amide formation is lower than the formation of the by-product acrylic acid [54]. Further, the double bonds of the reactants and products cause by-product formations as well as formation of polymerization products. As a result of optimization with methods of molecular engineering, a very high activity of the biocatalyst nitrile hydratase at low temperature is yielded, enabling a successful biotransformation that is superior to the chemical route. Here, the synthesis is carried out at a low temperature of about 5°C, showing a conversion of 100%. [Pg.94]

Porous polymer materials, especially in particulate form, are of interest in a diverse range of applications, including controlled drug delivery, enzyme immobilization, molecular separation technology, and as hosts for chemical synthesis [101-104]. MS materials have been used as hosts for the template synthesis of nanoporous polymer replicas through in situ polymerization of monomers in the mesopores [105-108]. [Pg.221]

SCHEME 2.60 Synthesis of polythiophene via chemical oxidation polymerization. [Pg.185]

In the following, a number of integrated reaction-separation systems wiU be discussed, with emphasis on the application of polymeric membranes. As a result, the systems discussed will be Hmited to relatively low temperatures, typically below 120°C. In Section 13.2, appHcations of membranes in chemical synthesis will be described. Subsequently, in Section 13.3 various examples of membrane bioreactors will be discussed. [Pg.527]

As for heterogeneous olefin polymerization catalysis, the activity of rare-earth metal catalysts may be also enhanced in organic transformations by the use of silica supports or other carriers [7]. Indeed, several catalytic C-C and C-X (with X = H/D, Si, O) bond formation reactions as weU as functional group transformations witness to the potential of SOLn/AnC-based heterogeneous catalysts for fine chemical synthesis. [Pg.496]

Uses. Solvent for synthetic rubber and resins intermediate in chemical synthesis manufacture of polymerized synthetic materials... [Pg.640]

Carbon dioxide is a widely available, inexpensive, and renewable resource. Hence, its utilization as a source of chemical carbon or as a solvent in chemical synthesis can lead to less of an impact on the environment than alternative processes. The preparation of aliphatic polycarbonates via the coupling of epoxides or oxetanes with CO2 illustrates processes where carbon dioxide can serve in both capacities, i.e., as a monomer and as a solvent. The reactions represented in (1) and (2) are two of the most well-studied instances of using carbon dioxide in chemical synthesis of polymeric materials, and represent environmentally benign routes to these biodegradable polymers. We and others have comprehensively reviewed this important area of chemistry fairly recently. Nevertheless, because of the intense interest and activity in this discipline, regular updates are warranted. [Pg.3]

Segal, D., Chemical Synthesis of Advanced Ceramic Materials, Cambridge Univ. Press, New York, 1991. Sehanobish K., H. T. Pham, and C. P. Bosnyak, Polycarbonates (Overview), in Polymeric Materials Encyclopedia, J. C. Salamone, ed., CRC Press, Boca Raton, FL, 1996. [Pg.193]

Most modern materials are formed empirically by solid-state methods. These methods generally involve more processing activity than chemical synthesis (for example, sintering of ceramic powders, modifying concrete by polymers, thermomechanical processing of alloys, layering polymeric membranes for... [Pg.6]

The inter-relationship between colloid and polymer chemistries is completed by colloidal polymer particles. The formation of 50-nm-diameter, 100- to 200-nm-long polyaniline fibrils in a poly(acrylic acid)-template-guided polymerization, similar in many ways to those produced from polymerized SUVs (see above), provides a recent example of polymer colloids [449], The use of poly(styenesulfonic acid) as a template yielded globular polyaniline particles which were found to be quite different morphologically from those observed in the regular chemical synthesis of polyaniline [449]. [Pg.89]


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See also in sourсe #XX -- [ Pg.5 ]




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