Quaternary extractants

The aqueous solution (A) contained the non-extractable quaternary bases. It was acidified with hydrochloric acid, filtered and precipitated with concentrated Mayer s reagent (50 g. of mercuric chloride, 200 g. of potassium iodide, 400 cc. of water), added with constant stirring. The precipitate was filtered, suspended in hot water, and hydrogen sulfide was bubbled through the suspension until all the mercury was precipitated as sulfide. The hot filtered solution on cooling yielded candicine iodide (hordenine methiodide) in straw-colored needles. The salt was recrystallized from hot water with the aid of charcoal and yielded colorless crystals, which melted at 234°. The mother liquors contained only small amounts of candicine. Total yield 16.4 g. of candicine iodide 2% of candicine on the dry plant. 

MeOH extract is POLAR EXTRACT (quaternary alkaloids and /V-oxides)... 

Some less reactive tertiary amines can be mixed with an excess of methyl toluene-/)-sulphonate, m.p. 28 , and the mixture (without a solvent) heated to a much higher temperature. The mixture is allowed to cool, but before solidification occurs, it is thoroughly stirred with ether to extract unused sulphonate, and the insoluble quaternary metho-toluene-/)-sulphonate may then crystallise. If ciystallisation does not occur, dissolve this residue in ethanol and treat one portion with ethanolic picric acid (to precipitate the methopicrate) and another portion with cold concentrated ethanolic sodium iodide (to precipitate the methiodide). (M.ps. of the siilphon.ates, pp. 553 -554.)... 

A typical composition of the catholyte is adiponitrile, 15 wt % acrylonitrile, 15 wt % quaternary ammonium salt, 39 wt % water, 29 wt % and by-products, 2 wt %. Such a solution is extracted with acrylonitrile and water, which separates the organics from the salt that can be returned to the cell. 

Anionic extractants are commonly based on high molecular weight amines. Metal anions such as MnO or ReO can be exchanged selectively with inorganic anions such as Cl or The equiHbrium for a quaternary onium compound of organic radicals R for two anion species A and B ... 

Basic Extractants. Only long-chain quaternary ammonium salts, R3NCH3 X , ia which R represents Cg—0 2 groups and X nitrate or thiocyanate, are effectively used for REE separations (see Quaternary ammonium compounds). The extractant reacts with REE according to an anion-exchange reaction ... 

EFFECT OF QUATERNARY AMMONIUM SAET EXCHANGE CENTER STERIC ACCESSIBILITY ON EXTRACTION OF CADMIUM BROMIDE COMPLEXES... 

The quaternary ammonium salts (QAS) are widely used as ionofores of ion-selective electrodes and extractants of metals halogenic anion complexes. The influence of the QASes nature with various methyl groups contents on the cadmium extraction from bromide media has been investigated. 

ANION-EXCHANGE EXTRACTION OF ZINC THIOCYANATE COMPLEXES BY NON-SYMMETRIC QUATERNARY AMMONIUM SALTS... 

High tendency of ZnfSCN) ion to extraction into organic phase is widely used for zinc determination by extraction photometry method. Recently it was shown that when single-chai ged anions ai e exchanged for double-chai ged ones, the selectivity of this process depends on the number of methyl substitutients in quaternary ammonium salt (QAS) cation. 

The process of isolation finally adopted by the former authors consists in precipitating as reineckates the water-soluble bases contained in a methyl alcoholic extract of the curare. The mixed reineckates are further purified, by solution in acetone and precipitation with water as often as may be necessary. The product so cleaned represents the bulk of the biological activity of the crude drug the mother liquors may contain curine (p. 374), which indicates a menisperm as one of the components of such curares. The mixed reineckates are then fractionated chromato-graphically over alumina and the components isolated as chlorides by the use of silver sulphate and barium chloride in succession. This process has been modified in detail by Schmid and Karrer, who have also found that with their curare, the more soluble reineckate fraction includes less potent quaternary alkaloids. 

In some cases, the Q ions have such a low solubility in water that virtually all remain in the organic phase. ° In such cases, the exchange of ions (equilibrium 3) takes place across the interface. Still another mechanism the interfacial mechanism) can operate where OH extracts a proton from an organic substrate. In this mechanism, the OH ions remain in the aqueous phase and the substrate in the organic phase the deprotonation takes place at the interface. Thermal stability of the quaternary ammonium salt is a problem, limiting the use of some catalysts. The trialkylacyl ammonium halide 95 is thermally stable, however, even at high reaction temperatures." The use of molten quaternary ammonium salts as ionic reaction media for substitution reactions has also been reported. " " ... 

These studies show that the thiospinel structure is quite flexible with opportunity for cation vacancies at the 8 a site. Our investigation on such cation-deficient thiospinels is significant in that it shows that additional vacancies are possible in the 8 a site. Most of the cation-deficient compounds known earlier (predominantly copper compounds) were obtained by extraction of Cu by using various oxidizing reagents. These studies show that such cation-deficient quaternary thiospinels can also be obtained by direct solid-state reactions. 

Figure 11.17a to Figure 11.17d show densitograms from the separation of Che-lidonium majus quaternary alkaloids. Various volumes of the extract solution of the same concentration, from 0.2 to 1.6 ml, were introduced to the adsorbent layer. Thus, the following portions of extract of 0.25, 0.5, 1, and 2 mg were chromatographed by the use of threefold development with the multicomponent eluent. The densitograms depict fast loss of resolution with the increase of the introduced sample [114]. 

---