Alkaline earth cation

Simplest examples are prepared by the cyclic oligomerization of ethylene oxide. They act as complexing agents which solubilize alkali metal ions in non-polar solvents, complex alkaline earth cations, transition metal cations and ammonium cations, e.g. 12—crown —4 is specific for the lithium cation. Used in phase-transfer chemistry. ... 

Table 12. Langmuir Constants for the Absorption of Alkaline-Earth Cations on Manganese Dioxide ...

The presence of metal salts, particularly those containing alkaline-earth cations and/or haUdes, cause some shifts in the polyborate equiUbria. This may result from direct interaction with the boron—oxygen species, or from changes in the activity of the solvent water (63). 

Oxide superconductors have been known since the 1960s. Compounds such as niobium oxide [12034-57-0] NbO, TiO, SrTi02, and AWO, where A is an alkah or alkaline earth cation, were found to be superconducting at 6 K or below. The highest T observed in oxides before 1986 was 13 Kin the perovskite compound BaPb Bi O, x = 0.27. Then in 1986 possible superconductivity at 35 K in the La—Ba—Cu—O compound was discovered (21). The compound composition was later determined to be La 85 A the Y—Ba—Cu—O system was pubUshed in 1987 and reported a transition... 

The addition of various alkali and alkaline earth cations to the cyclooligomerization of ethylene oxide by Dale and Daasvatn also provides strong presumptive evidence for the template effect. Recently, Reinhoudt, de Jong and Tomassen utilized several metal fluorides to effect crown formations . The reaction rates were found to be in the order Cs > Rb > > Na LE. Such an order would be expected on the basis of binding... 

We have not attempted to cover all or even most aspects of crown chemistry and some may say that the inclusions are eclectic. We felt that anyone approaching the field would need an appreciation for the jargon currently abounding and for the so-called template effect since the latter has a considerable bearing on the synthetic methodology. We have, therefore, included brief discussions of these topics in the first two chapters. In chapters 3—8, we have tried to present an overview of the macrocyclic polyethers which have been prepared. We have taken a decidedly organic tack in this attempting to be comprehensive in our inclusion of alkali and alkaline earth cation binders rather than the compounds of use in transition metal chemistry. Nevertheless, many of the latter are included in concert with their overall importance. 

Alkaline earth cations [5] methanol-hydrochloric acid (25%) (80 -I- 20). 

Reaction of Na2Se and Na2Sc2 with Se in the presence of ethanolic solutions of tetraalkyl-ammonium halides and catalytic amounts of I2 yields dark green or black crystalline polyselenides (jc = 3,5-9) depending on the conditions used and the particular cation selected. Tetraphenylphosphonium salts and crown ether complexes of alkali or alkaline earth cations in dimethylformamide solution can also be used. " )... 

Other recent works in this field, studies on the transport of alkali and alkaline earth cations with p-zerr-butyl calix[n]arene esters and amides, were carried out by Arnaud-Neu et al. [20] and Casnati et al. [21]. They prepared 1,3-alternate calix[4]arene-crown-6 as a new class of cesium selective ionophore. 

Group IV cations have soluble chlorides and sulfides, so they are still in solution at this point. The alkaline earth cations (Mg2, Ca2+. Ba2+) are precipitated as carbonates... 

Specificity for alkali and alkaline earth cations of synthetic and natural organic complexing agents in membranes. W. Simon, W. E. Morf and P. C. Meier, Struct. Bonding (Berlin), 1973, 16, 113-160 (123). 

Simon, W., Morf, W. E., Meier, P. Ch. Specificity of Alkali and Alkaline Earth Cations of Synthetic and Natural Organic Complexing Agents in Membranes. Vol. 16, pp. 113-160. 

Chesniuk et al. studied the transfer of alkali and alkaline-earth cations across phospholipid monolayers at water-1,2-DCE macrointerfaces by cyclic voltammetry. These authors considered the effect of the cation nature, the concentration of the transferring ion, and the applied potential (at the positive end of the polarization window), and noticed either an enhancement of the current or a blocking of the transfer process [13,14]. The enhancement factors observed were very much larger than in other studies, especially at... 

Figure 4.20 Separation of comon anions and alkaline earth cations by ion chronatography using conductivity detection.

Nair, L. M., Saari-Nordhaus, R., and Anderson, Jr., J. M., Simultaneous separation of alkali and alkaline-earth cations on polybudaiene-maleic acid-coated stationary phase by mineral acid eluents, /. Chromatogr., 640, 41,1993. 

Mobility tends to increase with increasing salinity because alkali- and alkaline-earth cations compete for adsorption sites on solids. 

Crown polyethers. Macrocyclic effects involving complexes of crown polyethers have been well-recognized. As for the all-sulfur donor systems, the study of the macrocyclic effect tends to be more straightforward for complexes of cyclic polyethers especially when simple alkali and alkaline earth cations are involved (Haymore, Lamb, Izatt Christensen, 1982). The advantages include (i) the cyclic polyethers are weak, uncharged bases and metal complexation is not pH dependent (ii) these ligands readily form complexes with the alkali and alkaline earth cations... 

The chapter on kinetics and mechanisms of complex formation and ligand substitution at alkali metal and alkaline earth cations elsewhere in this volume provides context and complementary discussion of these processes in relation to calcium. 

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