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Links preparation

Sulfuric acid, methanol, and polystyrene are other industrially important chemicals that depend on equilibrium reactions for their production. Choose one of these chemicals, or another industrial chemical. Research methods that are used to produce it, as well as the products that are derived from it. To start your research, go to the web site above and click on Web Links. Prepare a report that outlines what you learned. [Pg.369]

Figure 4.12 Sketch of the trapping of cyclics during the end-linking preparation of a network.292 Reproduced by permission of the American Chemical Society. Figure 4.12 Sketch of the trapping of cyclics during the end-linking preparation of a network.292 Reproduced by permission of the American Chemical Society.
Figure 9. Trapping of cyclic molecules during end-linking preparation of a network. (Reproduced from reference 47. Copyright 1987 American Chemical... Figure 9. Trapping of cyclic molecules during end-linking preparation of a network. (Reproduced from reference 47. Copyright 1987 American Chemical...
The oligonucleotide d(C)28 containing only phosphorothioate internucleotidic links (prepared chemically as a diastereoisomeric mixture) is a remarkably powerful linear competitive inhibitor of HIV reverse transcriptase, with a Ki value more than two orders of magnitude lower than that of all-phosphodiester d(C)28- Other d(C)28 analogues with cumulative runs of nine phosphorothioate links at the beginning, middle, and end of the sequence gave intermediate Ki values. Unfortunately, the all-phosphorothiate d(C)28 showed substantial inhibition also of DNA polymerases a and y, and may thus be cytotoxic. [Pg.258]

Sephadex A trade name for an insoluble hydrophilic substance prepared by cross-linking dextran, and used in gel filtration. It can also be linked to acidic or basic groups for ion exchange or to alkanes for the chromatography of lipophilic compounds. [Pg.356]

The successful preparation of polymers is achieved only if tire macromolecules are stable. Polymers are often prepared in solution where entropy destabilizes large molecular assemblies. Therefore, monomers have to be strongly bonded togetlier. These links are best realized by covalent bonds. Moreover, reaction kinetics favourable to polymeric materials must be fast, so tliat high-molecular-weight materials can be produced in a reasonable time. The polymerization reaction must also be fast compared to side reactions tliat often hinder or preclude tire fonnation of the desired product. [Pg.2515]

Copper(I) tends towards a tetrahedral coordination geometry in complexes. With 2,2 -bipyr-idine as a chelate ligand a distorted tetrahedral coordination with almost orthogonal ligands results. 2,2 -Bipyridine oligomers with flexible 6,6 -links therefore form double helices with two 2,2 -bipyridine units per copper(I) ion (J. M. Lehn, 1987,1988). J. M. Lehn (1990 U. Koert, 1990) has also prepared such helicates with nucleosides, e.g., thymidine, covalently attached to suitable spacers to obtain water-soluble double helix complexes, so-called inverted DNA , with internal positive charges and external nucleic bases. Cooperative effects lead preferentially to two identical strands in these helicates when copper(I) ions are added to a mixture of two different homooligomers. [Pg.345]

As early as 2500 bce m India indigo was used to dye cloth a deep blue The early Phoenicians discovered that a purple dye of great value Tyrian purple could be extracted from a Mediterranean sea snail The beauty of the color and its scarcity made purple the color of royalty The availability of dyestuffs underwent an abrupt change m 1856 when William Henry Perkin an 18 year old student accidentally discovered a simple way to prepare a deep purple dye which he called mauveme from extracts of coal tar This led to a search for other synthetic dyes and forged a permanent link between industry and chemical research... [Pg.4]

Hexamethylolmelamine can further condense in the presence of an acid catalyst ether linkages can also form (see Urea Eormaldehyde ). A wide variety of resins can be obtained by careful selection of pH, reaction temperature, reactant ratio, amino monomer, and extent of condensation. Eiquid coating resins are prepared by reacting methanol or butanol with the initial methylolated products. These can be used to produce hard, solvent-resistant coatings by heating with a variety of hydroxy, carboxyl, and amide functional polymers to produce a cross-linked film. [Pg.1017]

Liquid coating resins are prepared by reacting methanol or butanol with the initial hydroxyme-thylureas. Ether exchange reactions between the amino resin and the reactive sites on the polymer produce a cross-linked film. [Pg.1025]

Uses. Furfuryl alcohol is widely used as a monomer in manufacturing furfuryl alcohol resins, and as a reactive solvent in a variety of synthetic resins and appHcations. Resins derived from furfuryl alcohol are the most important appHcation for furfuryl alcohol in both utihty and volume. The final cross-linked products display outstanding chemical, thermal, and mechanical properties. They are also heat-stable and remarkably resistant to acids, alkaUes, and solvents. Many commercial resins of various compositions and properties have been prepared by polymerization of furfuryl alcohol and other co-reactants such as furfural, formaldehyde, glyoxal, resorcinol, phenoHc compounds and urea. In 1992, domestic furfuryl alcohol consumption was estimated at 47 million pounds (38). [Pg.80]


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Cross-linked polyacrylamide gels preparation

Cross-linking solution-based preparation

Enzyme-linked cell extract preparation

Enzyme-linked immunosorbent assay conjugate preparation

Enzyme-linked immunosorbent assay preparation

Plastics surface preparation cross-linking

Preparation of immunosorbents by cross-linking antigens

Randomly cross-linked preparation

Surface preparation Terms Links

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