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Neutralization cations

The Diels-Alder reaction of dienophiles 5.1a-e, containing neutral, cationic or anionic substituents, with diene 5.2 in the absence of Lewis acids is retarded by micelles of CTAB, SDS and C12E7. In the situation where the dienophile does not bind to the micelle, the reaction is inhibited because uptake of... [Pg.153]

Telechelic Ionomers. Low molecular weight polymers terminated by acid groups have been treated with metal bases to give ionomers in which the cations can be considered as connecting links in the backbones (67—71). The viscoelastic behavior of concentrated solutions has been linked to the neutralizing cation. [Pg.409]

Although UV spectra have been measured for a large number of substituted azoles, there has been no systematic attempt to explain substituent effects on such spectral maxima. Readily available data are summarized in Table 25, and some major trends are apparent. However, detailed interpretation is hindered by the fact that different solvents have been used and that in aqueous media it is not always clear whether a neutral, cationic or anionic species is being measured. Furthermore, values below 220 nm are of doubtful quantitative significance. [Pg.24]

It has been observed that the best neutral cation carriers have the synclinal arrangement of binding atoms in the backbone (see 7.2). Syntheses of both an aliphatic and aromatic ligand are shown below in Eqs. (7.12) and (7.13). [Pg.318]

Total Energy Values of and H Eorms OF lMIDAZO[4,5-/]QUINOLrNES FOR NEUTRAL, CATIONIC AND ANIONIC EORMS... [Pg.233]

As the above half-reactions proceed, a surplus of positive ions (Zn2+) tends to build up around the zinc electrode. The region around the copper electrode tends to become deficient in positive ions as Cu2+ ions are consumed. To maintain electrical neutrality, cations must move toward the copper cathode or, alternatively, anions must move toward the zinc anode. In practice, both migrations occur. [Pg.482]

The intent of this chapter is to establish a comprehensive framework in which the physicochemical properties of permeant molecules, hydrodynamic factors, and mass transport barrier properties of the transcellular and paracellular routes comprising the cell monolayer and the microporous filter support are quantitatively and mechanistically interrelated. We specifically define and quantify the biophysical properties of the paracellular route with the aid of selective hydrophilic permeants that vary in molecular size and charge (neutral, cationic, anionic, and zwitterionic). Further, the quantitative interrelationships of pH, pKa, partition... [Pg.235]

Bernard, P.J. "Neutral Cationic Emulsion Containing a Slow-Fracturing Hydrocarbon Binder," Chemical Abstracts. 78(12) 74596f (1973). [Pg.675]

DF calculations were carried out on CO complexes of small neutral, cationic, and anionic gold clusters Au with n= 1-6. The -coordination mode (terminal C-coordination) was found to be the most favorable one irrespective of the charge of the cluster, and cluster planarity is more stable for the bare clusters and their carbonyls. As expected, adsorption energies are greatest for the cationic clusters, and decrease with size. Instead, the adsorption energies of... [Pg.297]

In this chapter, we demonstrated that the restriction of building a compound with only one type of an element is not a restriction at all and a multitude of neutral, cationic as well as anionic polychalcogen structures is currently known. As expected for the more electronegative nonmetal (S) and meta metals (Se, Te), the bonding within these moieties is covalent and a small number of interactions, namely, p2-rap2 lone pair repulsion, n- and n -n bonding as well as p2- cr interactions, are sufficient to rationalize the structures and account for the bond lengths alternations or weak transannular interactions that are often found. [Pg.411]

Relative extraction efficiencies of polar polymeric neutral, cation, and anion exchange sorbents (HLB, MCX, and MAX) for 11 beta antagonists and 6 beta agonists in human whole blood were probed.109 Initial characterization of MCX and MAX for acidic and basic load conditions, respectively, showed that both the agonists and antagonists were well retained on MCX, while they were recovered from MAX in the wash with either methanol or 2% ammonia in methanol (see Table 1.6). Blood samples were treated with ethanol containing 10% zinc sulfate to precipitate proteins and the supernatants loaded in 2% aqueous ammonium hydroxide onto the sorbents. After a 30% methanol and 2% aqueous ammonia wash, the analytes were eluted with methanol (HLB), 2% ammonia in methanol (MCX), or 2% formic acid in methanol (MAX). The best recoveries were observed with MCX under aqueous conditions or blood supernatant (after protein precipitation) spiked sample load conditions (see Table 1.7). Ion suppression studies by post-column infusion showed no suppression for propranolol and terbutaline with MCX, while HLB and MAX exhibited suppression (see Figure 1.6). [Pg.12]

Extraction with Neutral Cation Exchange Solutions 215... [Pg.226]

Surfactants can be either found or synthesized to contain both hydrophobic and hydrophilic regions and can be cationic, anionic, or neutral. Cationic surfactants can be chosen to extract metals from soil. Of particular interest are those anionic surfactants that are naturally produced by plants and microorganisms because they can easily be broken down in soil once extraction has been accomplished. However, the use of surfactants for extracting metals has found limited use [27],... [Pg.244]

The radiation chemistry of polymers is therefore the chemistry of neutral, cation and anion radicals, cations and anions, and excited species. [Pg.4]

Fig. 2.1-18. Relationships between isoelectronic neutral, cationic and anionic polyborane bis(trimethylphosphine) compounds. Fig. 2.1-18. Relationships between isoelectronic neutral, cationic and anionic polyborane bis(trimethylphosphine) compounds.
The complex behaviour of pharmaceuticals in the sewage network and during subsequent wastewater treatment is correlated to the nature of their molecular structure, which may contain concomitant acidic and basic functional groups, as in the case of both ciprofloxacin and ceftazidime. This implies that these molecules may be considered as neutral, cationic, anionic or zwitterionic [53], according to the particular environmental conditions, which will consequently affect their behaviour. [Pg.149]

Surfactants used to make films containing MCs can be categorized as neutral, cationic, and anionic. [Pg.240]

The diffusion constant for Cu can also be discussed using this model. Because diffusion by singly charged cation vacancies, and by neutral cation vacancies, are both important, we may write... [Pg.81]

The halogen compounds are known for neutral, cationic and anionic species. These should be three, two and four coordinate, with T-shaped, angular and square planar coordination arrangements respectively. No crystallographic work has been reported on the simple species and the spectroscopic results are not always conclusive. [Pg.320]

The parfait-distillation method uses a sequential series of adsorbents to remove contaminants from water and vacuum distillation to recover unadsorbed materials. This method recovers a wide range of neutral, cationic, anionic, and hydrophobic contaminants. The first adsorbent, porous polytetrafluoroethylene (PTFE), removed humic acid and a broad range of hydrophobic compounds. PTFE was followed by Dowex MSC-1 and then Duolite A-162 ion-exchange resins. A synthetic hard water spiked parts-per-billion concentrations with 20 model compounds was used to evaluate the method. Poorly volatile, neutral, water-soluble species (glucose) cationic aromatics and most hydro-phobic compounds were recovered quantitatively. Model ampho-terics were removed from the influent but were not recovered from the adsorption beds. The recovery of model acids and bases ranged from 22% to 70% of the amount applied. [Pg.489]

Singly ionized and neutral cation vacancies can form in a similar way... [Pg.193]

The original interlamellar, charge-neutralizing cation can be readily replaced, as desired, by one (or possibly more) of a whole range of inorganic or organic cations. [Pg.339]

These metal cations are too large or have too low a charge to have an appreciable polarizing effect on the hydrating water molecules that surround them, so the water molecules do not readily release their protons. These cations are sometimes called neutral cations, because they have so little effect on the pH. [Pg.619]

Density functional theory studies arene chromium tricarbonyls, 5, 255 beryllium monocyclopentadienyls, 2, 75 chromium carbonyls, 5, 228 in computational chemistry, 1, 663 Cp-amido titanium complexes, 4, 464—465 diiron carbonyl complexes, 6, 222 manganese carbonyls, 5, 763 molybdenum hexacarbonyl, 5, 392 and multiconfiguration techniques, 1, 649 neutral, cationic, anionic chromium carbonyls, 5, 203-204 nickel rj2-alkene complexes, 8, 134—135 palladium NHC complexes, 8, 234 Deoxygenative coupling, carbonyls to olefins, 11, 40 (+)-4,5-Deoxyneodolabelline, via ring-closing diene metathesis, 11, 219... [Pg.93]


See other pages where Neutralization cations is mentioned: [Pg.178]    [Pg.540]    [Pg.977]    [Pg.186]    [Pg.100]    [Pg.588]    [Pg.21]    [Pg.30]    [Pg.332]    [Pg.225]    [Pg.276]    [Pg.192]    [Pg.175]    [Pg.78]    [Pg.109]    [Pg.117]    [Pg.163]    [Pg.361]    [Pg.148]    [Pg.664]    [Pg.85]    [Pg.590]   
See also in sourсe #XX -- [ Pg.469 ]




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