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Ammonium ions quaternary

Complex Ion Formation. Phosphates form water-soluble complex ions with metallic cations, a phenomenon commonly called sequestration. In contrast to many complexing agents, polyphosphates are nonspecific and form soluble, charged complexes with virtually all metallic cations. Alkali metals are weakly complexed, but alkaline-earth and transition metals form more strongly associated complexes (eg, eq. 16). Quaternary ammonium ions are complexed Htde if at all because of their low charge density. The amount of metal ion that can be sequestered by polyphosphates generally increases... [Pg.339]

Other common five-membered heterocyclic amines include imidazole and thiazole. Imidazole, a constituent of the amino acid histidine, has two nitrogens, only one of which is basic. Thiazole, the five-membered ring system on which the structure of thiamin (vitamin Bt) is based, also contains a basic nitrogen that is alkylated in thiamin to form a quaternary ammonium ion. [Pg.948]

Blackborow and Ridd51 studied the deuteration of aryl quaternary ammonium ions by deuterated sulphuric acid under second-order conditions (Table 173), and the results showed that, contrary to earlier beliefs, the positive nitrogen pole has... [Pg.261]

In each case, the N atom is sp hybridized, with one lone pair of electrons and three o-bonds. A quaternary ammonium ion is a tetrahedral ion of the form R4N, where as many as three of the R groups (which may all be different) can be replaced by H atoms. For example, the tetramethylammonium ion, (CH3)4N+, and the trimethylammonium ion, (CH3)3NH+, are quaternary ammonium ions. The amino group, the parent functional group of amines, is —NH2. [Pg.879]

The electrolytes Na", and Cl are second only to glucose in being the most frequently run hospital tests. Many clinical chemistry analyzers now contain an ISE module for electrolyte analysis. Most commonly the module will consist of a Na -glass electrode, a valinomycin/PVC electrode, a Ag/AgCl pellet or a quaternary ammonium ion/PVC electrode and a reference electrode. A selective electrode for the bicarbonate ion continues to elude workers in the field. An indirect measurement of HCOf must be made. The sample is usually reacted with acid to evolve carbon dioxide gas which is measured with a traditional Severinghaus type CO2 electrode. Alternatively, the sample is treated with base to convert HCO to CO3 and a carbonate ion-selective electrode is used In this manner, the complete primary electrolyte profile is obtained electrochemically. [Pg.61]

Bouchard, G., Carrupt, P. A., Testa, B., Gobry, V., Girault, H. H. The apparent lipophilicity of quaternary ammonium ions is influenced by Galvani potential difference, not ion-pairing a cyclic voltammetry study. Pharm. Res. 2001, 18, 702-708. [Pg.435]

If in the quaternary ion a /3-hydrogen is not available, as in tetramethyl-, benzyltrimethyl- or phenyltrimethylammonium hydroxide, reaction 4.101 cannot occur, but reaction 4.102 still can this means that the quaternary ammonium ions without a /1-hydrogen are appreciably more stable, so that the type of base concerned is mainly the commercially available one (in alcoholic solution) (CH3)4NOH appears especially attractive, although the (CH3)4N salts are less soluble in non-aqueous media than, for instance, (C4H9)4N salts. [Pg.298]

The azide form of the quaternary ammonium ion exchange resin IR-400 (which exhibits low lfiction-sensitivity) reacts with bromoform, analogously to dichloro-and dibromo-methane, to form the highly explosive triazidomethane. Solutions of above 50% concentration explode in contact with a pipette or on injection into a GLC inlet port. [Pg.157]

Quaternary ammonium ions have long been known to act as stmcture-directing agents in the crystallization of zeolites <1961JCS971 >. Millini and co-workers have more recently employed the azoniaspiro compounds 154,9, and 155 for this reason to produce novel microporous frameworks <1998MI199>. [Pg.1060]

Another way for covalent immobilisation is to synthesise indicator chemistry with polymerizable entities such as methacrylate groups (Figure 4). These groups can then be copolymerized with monomers such as hydrophobic methyl methacrylate or hydrophilic acryl amide to give sensor copolymers. In order to obtain self-plasticized materials, methacrylate monomers with long alkyl chains (hexyl or dodecyl methacrylate) can be used. Thus, sensor copolymers are obtained which have a Tg below room temperature. Similarly, ionophores and ionic additives (quaternary ammonium ions and borates) can be derivatised to give methacrylate derivatives. [Pg.307]

The hydroxyethyl quaternary ammonium ion in (20) is a weak acid the pATa-value of the non-micellizing model compound, choline, is 12.8 (Haber-field and Pessin, 1982). Reactions of the alkoxide zwitterion are therefore followed at relatively high pH, and from the variation of rate constant with... [Pg.263]

This situation is illustrated qualitatively in Fig. 5 where an indicator, BH, is located close to quaternary ammonium ion head groups and will be deprotonated by hydroxide ions which are in their vicinity. But the functional hydroxyl groups are in the diffuse layer and their deprotonation will... [Pg.264]

The effect of mixtures of surfactants and polyelectrolytes on spontaneous, water-catalysed hydrolysis (Fadnavis and Engberts, 1982) was mentioned in Section 4, but mixtures of functionalized polyelectrolytes and cationic surfacants are effective deacylating agents (Visser et al., 1983). Polymerized isocyanides were functionalized with an imidazole group and the deacylation of 2,4-dinitrophenyl acetate in the polyelectrolyte was speeded by addition of single or twin chain quaternary ammonium ion surfactants, up to a plateau value. Anionic surfactants had essentially no effect. It is probable that the cationic surfactants accelerate the reaction by increasing the deprotonation of the imidazole groups. [Pg.265]

Section 6) can be applied to reactions of the non-micellizing ions. The second-order rate constants at the surface of a functionalized micelle and tri-n-octylammonium ion are very similar (Biresaw et al., 1984 Bunton and Quan, 1984). Some examples are given in Table 11. In some reactions mixtures of functional and nonfunctional amphiphile were used and allowance was made for the dilution. The second-order rate constants in Table 11 are calculated using nucleophile concentrations written as mole ratios of nucleophile to quaternary ammonium ion because it is not obvious how a molar volume element of reaction can be estimated for the tri-n-octylammo-nium ions. [Pg.275]

Most of the attempted asymmetric reductions have used sodium borohydride in conjunction with quaternary ammonium catalysts. Recently, the solution structures of ion pairs formed by quaternary ammonium ions derived from quinine with borohydride ion have been characterized by nuclear magnetic resonance methods in CDC13.1741... [Pg.139]

Another mode of termination by monomer, which has been suggested for the polymerization of N-vinylcarbazole, is formation of a quaternary ammonium ion from the growing cation and the monomer [25] which is essentially the same as reaction (XIa). [Pg.145]

Anthoni U, Nielsen PH, Smith-Hansen L, Wium-Andersen S, Christophersen C (1987) Charamin, a quaternary ammonium ion antibiotic from the green alga Chara globularis. J Org Chem 52 694-695... [Pg.116]


See other pages where Ammonium ions quaternary is mentioned: [Pg.939]    [Pg.257]    [Pg.2]    [Pg.939]    [Pg.169]    [Pg.812]    [Pg.956]    [Pg.172]    [Pg.19]    [Pg.879]    [Pg.940]    [Pg.963]    [Pg.1037]    [Pg.312]    [Pg.180]    [Pg.184]    [Pg.339]    [Pg.29]    [Pg.148]    [Pg.150]    [Pg.152]    [Pg.165]    [Pg.167]    [Pg.9]    [Pg.221]    [Pg.253]    [Pg.255]    [Pg.264]    [Pg.274]    [Pg.169]    [Pg.598]   
See also in sourсe #XX -- [ Pg.148 , Pg.150 , Pg.152 , Pg.167 ]

See also in sourсe #XX -- [ Pg.45 ]

See also in sourсe #XX -- [ Pg.50 ]




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