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Reaction through functionality

Often used as mixtures, the telomers are subsequently converted to commercial surfactants and stain-resistant fiber finishes through functionalizing steps using standard chemical reactions of the C—1 bond. [Pg.269]

Covalent crosslinking. Acrylic polymers can be covalently crosslinked through direct reaction between functional monomers in the polymer itself or by the addition of a crosslinking reagent, which typically reacts with the functional groups or polymer backbone in the PSA. In general, acrylic polymers are very... [Pg.494]

Reactive compatibilization of engineering thermoplastic PET with PP through functionalization has been reported by Xanthos et al. [57]. Acrylic acid modified PP was used for compatibilization. Additives such as magnesium acetate and p-toluene sulfonic acid were evaluated as the catalyst for the potential interchange or esterification reaction that could occur in the melt. The blend characterization through scanning electron microscopy, IR spectroscopy, differential scanning calorimetry, and... [Pg.673]

A different type of catalysis is observed using proline as a catalyst.166 Proline promotes addition of acetone to aromatic aldehydes with 65-77% enantioselectivity. It has been suggested that the carboxylic acid functions as an intramolecular proton donor and promotes reaction through an enamine intermediate. [Pg.131]

As the latest example in this section, the synthesis of clavolonine [314] by the group of Evans is mentioned [315]. Through the action of a multiple anionic domino reaction a functionalized linear carbon chain was converted into the polycyclic architecture of the natural product. [Pg.142]

The transformation of the chain end active center from one type to another is usually achieved through the successful and efficient end-functionalization reaction of the polymer chain. This end-functionalized polymer can be considered as a macroinitiator capable of initiating the polymerization of another monomer by a different synthetic method. Using a semitelechelic macroinitiator an AB block copolymer is obtained, while with a telechelic macroinitiator an ABA triblock copolymer is provided. The key step of this methodology relies on the success of the transformation reaction. The functionalization process must be 100% efficient, since the presence of unfunctionalized chains leads to a mixture of the desired block copolymer and the unfunctionalized homopolymer. In such a case, control over the molecular characteristics cannot be obtained and an additional purification step is needed. [Pg.62]

In the condensation polymerisation or step growth polymerisation, the polymer molecules are built up through many separate reaction of functional groups. [Pg.8]

Coenzymes facilitate chemical reactions through a range of different reaction mechanisms, some of which will be discussed in detail in this review. However, in all cases structural features of the coenzyme allow particular reactions to proceed along a mechanistic pathway in which reaction intermediates are more thermodynamically and kinetically accessible. When incorporated into apoen-zyme active sites, the coenzyme reactivity is influenced by a well-defined array of amino acid functional groups. For a given coenzyme, the particular array of amino acids presented by the different apoenzymes can drastically alter the degree of rate acceleration and product turnover and can specify the nature of the reaction catalyzed. [Pg.3]

The flavin-based coenzymes flavin adenine dinucleotide (FAD) and flavin mononucleotide (FMN) are associated with a wide variety of enzymes that catalyze reactions in critical biosynthetic and catabolic processes (Fig. 16). Unlike other coenzymes, the reactions catalyzed do not conserve specific mechanistic pathways. In each case the apoenzyme serves to steer the course of the reaction through specific interactions with substrate and coenzyme [55]. Nonetheless, there are common features of the interactions of the apoenzymes with the flavin which can be exploited in the design of functional peptides and proteins. [Pg.23]

Why did nature use an Fe-S cluster to catalyze this reaction, when an enzyme such as fumarase can catalyze the same type of chemistry in the absence of any metals or other cofactors One speculation would be that since aconitase must catalyze both hydrations and dehydrations, and bind substrate in two orientations, Fe in the comer of a cubane cluster may provide the proper coordination geometry and electronics to do all of these reactions. Another possibility is that the cluster interconversion is utilized in vivo to regulate enzyme activity, and thus, help control cellular levels of citrate. A third, but less likely, explanation is that during evolution an ancestral Fe-S protein, whose primary function was electron transfer, gained the ability to catalyze the aconitase reaction through random mutation. [Pg.368]

Chemical Degradation is promoted by chemical reaction through additives in the plastic, e.g. metals, functional groups and is operative under all conditions. Fragments produced may biodegrade. [Pg.3]

Coordination polymers can be prepared by a number of routes, among which the three most common being (1) preformed coordination metal complexes polymerized through functional groups where the actual polymer-forming step may be a condensation or addition reaction ... [Pg.371]

The spleen is an organ, the main functions of which are the formation and purification ofblood. Blood from the spleen and intestine is passed through the portal vein to the liver for further reactions. The functions of the lungs, kidneys, and liver are described later in the chapter. The coronary arteries, which branch from the aorta, supply blood to the muscles of the heart. [Pg.254]

However, often it is difficult to produce suitable graft or block copolymers for important commercial applications. Alternatively, these compatibilizing copolymers can be generated in situ during the blend preparation through polymer-polymer grafting reactions using functionalized polymers (38). [Pg.225]

Figure 12.4 Comparison of the reaction rate functions Eqs. 12-27 (curve 1) and 12-28 (curve 2). The straight line through the origin indicates the initial slope of size k. Half-saturation concentrations are at ln2 (J/k) and (J/k), respectively. Parameter values J= 1, k = 1. Figure 12.4 Comparison of the reaction rate functions Eqs. 12-27 (curve 1) and 12-28 (curve 2). The straight line through the origin indicates the initial slope of size k. Half-saturation concentrations are at ln2 (J/k) and (J/k), respectively. Parameter values J= 1, k = 1.
Equilibrium of transamination reactions For most transamina tion reactions, the equilibrium constant is near one, allowing the reaction to function in both amino acid degradation through removal of a-amino groups (for example, after consumption of a protein-rich meal), and biosynthesis through addition of amino groups to the carbon skeletons of a-keto acids (for example, when the supply of amino acids from the diet is not adequate to meet the synthetic needs of cells). [Pg.249]

Poly(vinylbenzyl chloride) (VBC) is an ideal starting material onto which a variety of functional groups can be attached through relatively simple reactions and mild reaction conditions. Functionalized polymers are of interest in a variety of applications including but not limited to fire retardants, selective sorption resins, chromatography media, controlled release devices and phase transfer catalysts. An example of the wide applicability of functionalized polymers is provided by trimethyl ammonium functionalized poly(VBC). [Pg.97]


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