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Ion functional groups

Excited states of iminium ion functional groups have been shown to undergo one electron reduction readily from a number of unlikely one electron donors such as simple olefins, aromatic hydrocarbons, alcohols and ethers. PET reaction from these systems have led to the development of synthetically important carbon-carbon bond forming methodology. A number of studies... [Pg.209]

Keywords. Palladium catalyst, OrganosUicate, Fluoride ion. Functional group tolerance... [Pg.61]

Anion exchange resins have bonded quaternary ammonium ion functional groups ( 3 mmol/g resin) which are ion paired to exchangeable anions. For example, the reaction of a Cl-loaded resin with some singly charged anion, X, is... [Pg.242]

A saturated alkyl group does not exhibit functionality. It is not a d -synthon, because the functional groups, e.g. halide or metal ions, are lost in the course of the reaction. It functions as an alkyl synthon. Alkenyl anions (R. West, 1961) on the other hand, constitute d -synthons, because the C = C group remains in the product and may be subject to further synthetic operations. [Pg.5]

Carbocations stabilized by functional groups can also effect 3-alkylalion of indoles. From a synthetic point of view the most important are jV.jV-dialkyl-methyleneiminium ions which can be generated under Mannich conditions from formaldehyde and secondary amines[13]. The products, 3-(A/,A-dialkyl-aminornethyl)indoles, are useful synthetic intermediates (see Chapter 12). [Pg.106]

Polarography is used extensively for the analysis of metal ions and inorganic anions, such as lOg and NOg. Organic compounds containing easily reducible or oxidizable functional groups also can be studied polarographically. Functional groups that have been used include carbonyls, carboxylic acids, and carbon-carbon double bonds. [Pg.516]

Fig. 3. (a) Chemical stmcture of a synthetic cycHc peptide composed of an alternating sequence of D- and L-amino acids. The side chains of the amino acids have been chosen such that the peripheral functional groups of the dat rings are hydrophobic and allow insertion into Hpid bilayers, (b) Proposed stmcture of a self-assembled transmembrane pore comprised of hydrogen bonded cycHc peptides. The channel is stabilized by hydrogen bonds between the peptide backbones of the individual molecules. These synthetic pores have been demonstrated to form ion channels in Hpid bilayers (71). [Pg.202]

Ion-exchange resins are categorized by the nature of functional groups attached to a polymeric matrix, by the chemistry of the particular polymer in the matrix, and by the porosity of the polymeric matrix. There are four primary types of functionaHty strong acid, weak acid, strong base, and weak base. Another type consists of less common stmctures in specialty resins such as those which have chelating characteristics. [Pg.371]

Functionalization. Copolymers do not have the abiHty to exchange ions. Such properties are imparted by chemically bonding acidic or basic functional groups to the aromatic rings of styrenic copolymers, or by modifying the carboxyl groups of the acryHc copolymers. There does not appear to be a continuous functionalization process on a commercial scale. [Pg.373]

Capacity. Capacity is a measure of the quantity of ions, acid, or base removed (adsorbed) by an ion-exchange material. The quantity removed is direcdy correlated with the number of functional groups. Capacity is reported ia several different ways, but requites further definition because the word by itself does not cover ad situations. Total capacity is a measure of ad the functional groups on a resia and is recorded on a weight as wed as a volume basis. [Pg.377]


See other pages where Ion functional groups is mentioned: [Pg.13]    [Pg.437]    [Pg.506]    [Pg.117]    [Pg.3084]    [Pg.12]    [Pg.28]    [Pg.13]    [Pg.437]    [Pg.506]    [Pg.117]    [Pg.3084]    [Pg.12]    [Pg.28]    [Pg.2521]    [Pg.111]    [Pg.48]    [Pg.1113]    [Pg.1117]    [Pg.1147]    [Pg.8]    [Pg.346]    [Pg.346]    [Pg.547]    [Pg.590]    [Pg.591]    [Pg.265]    [Pg.209]    [Pg.209]    [Pg.305]    [Pg.207]    [Pg.371]    [Pg.371]    [Pg.374]    [Pg.376]    [Pg.377]    [Pg.377]    [Pg.378]    [Pg.378]    [Pg.379]    [Pg.380]    [Pg.380]    [Pg.384]    [Pg.384]    [Pg.384]    [Pg.386]    [Pg.387]   
See also in sourсe #XX -- [ Pg.132 ]




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