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Of the active groups

The efficacy of ring fluorination depends on the nature and position of the activating group, Y, m the aromatic ring The relative extent of for N (CH3)3 displacement decreases in the following order for Y p-NOy (71%), p-CN (24%), P-CH3CO (15%), p CHO (<5%) = m NO2 (<5%) This fluorodequaternization technique was subsequently adapted to prepare numerous NC A (no-camer-added) F-labeled aryl fluorides [7J, 74]... [Pg.279]

Therefore, the graft copolymerization of vinyl monomers onto macromolecules having active an pendant group can be achieved either by redox initiation with a Ce(IV) ion or by photo-induced charge-transfer initiation with BP, depending on the structure of the active groups. [Pg.552]

Some typical transfer constants for allyl sulfides are given in Table 6.7. The values of Clt for these reagents are less dependent on the particular monomer than those for halocarbons (Table 6.2) or thiol transfer agents (Table 6.4). The low transfer constant of 32 demonstrates the importance of the activating group Z (cf. 11). [Pg.299]

The committee estimates that, in a given year, somewhere between 10 and 25 of the active groups in surface and interfacial engineering will need to acquire a major instrument for adaptation and use. A funding level of 5 million per year for major dedicated instrumentation can meet most of these needs. [Pg.205]

Experiments were made with pure 2-propanol samples stored for six months in white glass containers, which were half full and exposed to the light. It could be proved that peroxides form in these conditions. The experiment showed that peroxidation is faster when a ketone is present. The fact that this oxidation only takes place with secondary alcohols shows that it affects the hydrogen atom in the a position of the active group, (atom that is more reactive than a primary hydrogen), and not the actual function. [Pg.253]

Chain gro tvth polymerization begins when a reactive species and a monomer react to form an active site. There are four principal mechanisms of chain growth polymerization free radical, anionic, cationic, and coordination polymerization. The names of the first three refer to the chemical nature of the active group at the growing end of the monomer. The last type, coordination polymerization, encompasses reactions in which polymers are manufactured in the presence of a catalyst. Coordination polymerization may occur via a free radical, anionic, or cationic reaction. The catalyst acts to increase the speed of the reaction and to provide improved control of the process. [Pg.41]

The symposium on which this book is based assembled the results of worldwide research on surfactant structure/performance relationships by most of the active groups throughout the world. Most of the papers included here embody recent research results a few are invited overview papers. [Pg.1]

Carbon-oxygen bonds adjacent to an aromatic ring or an alkene function can be cleaved by reduction at very negative potentials [1]. The process is often followed by reduction of the activating group as in 1. In these processes, the reduction potential of the activating group controls the electrode potential required. Thus an... [Pg.161]

Besides these important procedures, research to discover new, original, pharmaceutical substances was also started. The first important success came in 1954 as the fruit of research in the field of cytostatics. It was Vargha s idea to combine cytostatically active groups with carbohydrates in the hope that, by using sugars as carriers, the high toxicity of the active groups would be decreased. This... [Pg.6]

There are differences between the kinds of groups that absorb in the IR and those that are Raman active. Parts of Raman and IR spectra are complementary, each being associated with a different set of vibrational modes within a molecule. Other vibrational modes may be both Raman and IR active. The intensity or power of a Raman peak depends in a complex way on the polarizability of the molecule, the intensity of the source, and the concentration of the active group, as well as other factors. Raman intensities are usually directly proportional to the concentration of the active species. [Pg.377]

In Table 1, ion-exchangc resins are classified by type, active exchange group, and configuration of the active group on the polymer. Some of the proprietary resins are noi included. [Pg.863]

Using a surface-sulfonated ion exchange resin (refs. 11-12), optimum accessibility of the active groups which are almost exclusively located at the inner surface of the microparticles is attained. The measured reaction rate (see Table 1) is about ten times higher than that of the identically cross-linked Lewatit SPC 11B. [Pg.492]

The addition of unstabilized a-nitrile carbanions to a,3-unsaturated carbonyl acceptors affords predominantly 1,2-addition products, 56 while lithiated acetonitrile derivatives having a-alkoxy, a-aromatic, a-dialkylamino, a-phenylselenyl, a-phenylthio or a-trimethylsilyl substituents afford 1,4-adducts. However, some of these are acyl anion equivalents (Section 1.2.2.3.2) so this discussion is limited to a-stabi-lized nitriles in which the nitrile function is retained after removal of the activating group. Notable examples are trimethylsilylacetonitrile (208),157 phenylthioacetonitriles (209),158a b phenylselenylacetoni-... [Pg.111]

On application of equation (28), respectively (29), it was found that, as regards simplifications, it was necessary only to assume the concentration of the active groups and the coefficients of diffusion to be constant, in order to be able to solve the flux equations. The osmosis could be accounted for. [Pg.324]

It must be borne in mind, however, that results may be affected unfavourably, because water transport has been neglected. If the concentrations of the outer solutions are very small compared with the concentrations of the active groups, to co-ions in the membrane can be... [Pg.332]

The reactions of Ru(CO)4(C2H4) with activated alkynes have been shown in some cases to yield metallacyclopentanes as well as metallacyclopentenes and metal-lacyclopentadienes, depending on the nature of the activating group (CF3 vs. C02Et)62 (Scheme 20). [Pg.177]


See other pages where Of the active groups is mentioned: [Pg.461]    [Pg.287]    [Pg.310]    [Pg.336]    [Pg.248]    [Pg.315]    [Pg.43]    [Pg.946]    [Pg.297]    [Pg.43]    [Pg.48]    [Pg.23]    [Pg.75]    [Pg.70]    [Pg.45]    [Pg.340]    [Pg.366]    [Pg.462]    [Pg.160]    [Pg.226]    [Pg.461]    [Pg.893]    [Pg.47]    [Pg.49]    [Pg.807]    [Pg.313]    [Pg.326]    [Pg.53]    [Pg.635]    [Pg.226]    [Pg.69]    [Pg.72]    [Pg.14]   
See also in sourсe #XX -- [ Pg.72 ]




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Activating groups

Activation of the carbonyl group

Active groups

Group Activation

Preparation of polymethylphenylsiloxanes with active hydrogen atoms and vinyl groups at the silicon atom

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