Potassium halide, structure

In our investigation we have used BiOHal electrodes obtained by the exhaustive anodic oxidation of a bismuth layer with a thickness of about 200 nm on a platinum substrate in aqueous solutions of potassium halides (KHal) using the method previously reported in full details [93]. The resulted BiOHal films exhibited porous structure (according to the BET data, the surface area was 47, 25, and 6 m2/g for BiOCl, BiOBr, and... 

The ammonium ion is about the same size ( ,. = 151 pm) as the potassium ion (r = 152 pm) and this is a useful fact to remember when explaining the resemblance in properties between these two ions. For example, the solubilities of ammonium salts are similar to those of potassium salts. Explain the relation between ionic radius and solubility. On the other hand, all of the potassium halides crystallize in the NaCI structure with C.N. = 6 (see Chapter 4). but none of the ammonium halides does so. The coordination numbers of the ammonium halides are either four or eight. Suggest an explanation. 

Work with cations includes examination of the viscosity effects of sodium and potassium halides on solutions of xylose (structure-making and structurebreaking trends were studied), calorimetric analysis of the interaction of calcium ions with D-galactose, myo-inositol, and lactose, and conductance... 

Thermal parameters affecting the crystallization of sorbitol have been studied depending on conditions, two crystalline modifications can arise, and a process for the rapid crystallization of molten sorbitol was proposed. Compression parameters of crystalline xylitol have also been reported. The viscosity of concentrated aqueous solutions of sodium and potassium halides in presence of D-mannitol has been studied the viscosity was related to the structure-making or structure-breaking effect of the salt in solution. ... 

The potassium halides have a phase transition at about 20 kilo-bars, going from the f.c.c. (NaCl) to the s.c. (CsCl) structure. In view of the results discussed above for the two phases at low pressure one would predict a displacement of the excited state outward with respect to the ground state, and thus a blue shift at the transition. Figure 17 shows the results for KCl, KBr, and KI. The... 

The solubility of ionic substances in relatively nonpolar aprotic solvents can be greatly enhanced by using catalytic quantities of macrocyclic polyethers, such as 18-crown-6, the structure of which is shown in Fig. 5.5. These macrocyclic ethers selectively solvate the cation, both enhancing solubility and also leaving the anion in a very weakly solvated state. The anions behave under these conditions as highly reactive species, sometimes termed naked anions. A study of the relative rates of nucleophilic substitution on benzyl tosylate by potassium salts in acetonitrile in the presence of 18-crown-6 revealed a pronounced leveling effect. " All the potassium halides (fluoride, chloride, bromide, and iodide) were approximately equal in their reactivity. Potassium acetate was observed to be almost ten times more reactive than potassium iodide under these conditions—a reversal of the normal reactivity of acetate ion versus iodide ion in nucleophilic substitution reactions. As measured by cHji values in Table 5.5, iodide is 3 log units, i.e., 10 times, more reactive than acetate ion in the protic solvent methanol. 

Soper AK, Weckstrom K. (2006) Ion solvation and water structure in potassium halide aqueous solutions. Biophys Chem 124 180-191. 

In the second part of the 20th century, the tantalum capacitor industry became a major consumer of tantalum powder. Electrochemically produced tantalum powder, which is characterized by an inconsistent dendrite structure, does not meet the requirements of the tantalum capacitor industry and thus has never been used for this purpose. This is the reason that current production of tantalum powder is performed by sodium reduction of potassium fluorotantalate from molten systems that also contain alkali metal halides. The development of electronics that require smaller sizes and higher capacitances drove the tantalum powder industry to the production of purer and finer powder providing a higher specific charge — CV per gram. This trend initiated the vigorous and rapid development of a sodium reduction process. 

Tantalum powder is produced by reduction of potassium heptafluoro-tantalate, K2TaF7, dissolved in a molten mixture of alkali halides. The reduction is performed at high temperatures using molten sodium. The process and product performance are very sensitive to the melt composition. There is no doubt that effective process control and development of powders with improved properties require an understanding of the complex fluoride chemistry of the melts. For instance, it is very important to take into account that changes both in the concentration of potassium heptafluorotantalate and in the composition of the background melt (molten alkali halides) can initiate cardinal changes in the complex structure of the melt itself. 

The key cyclization in Step B-2 was followed by a sequence of steps that effected a ring expansion via a carbene addition and cyclopropyl halide solvolysis. The products of Steps E and F are interesting in that the tricyclic structures are largely converted to tetracyclic derivatives by intramolecular aldol reactions. The extraneous bond was broken in Step G. First a diol was formed by NaBH4 reduction and this was converted via the lithium alkoxide to a monomesylate. The resulting (3-hydroxy mesylate is capable of a concerted fragmentation, which occurred on treatment with potassium f-butoxide. 

Bis[(tris(isopropyl)cyclopentadienyl)]zinc (Zn C5(Pr1)3H2 2, 21) and bis[(tetrakis(isopropyl)cyclopentadienyl)]zinc (Zn C5(Pr1)4H 2, 22) were synthesized from the respective potassium cyclopentadienides and zinc iodide as shown in Scheme 18.50 The same slipped sandwich compounds were also isolated from zinc-reduced VC13 solutions when they were treated with these alkali metal cyclopentadienides at room temperature.51 The outcomes of these reactions suggest that zincocenes are likely intermediates in the syntheses of transition metal metallocenes, in which the metal halides have been pre-reduced with zinc. The solid-state structure of Zn G5(Pr1)4H 2 is shown in Figure 10. The sole... 

The Gabriel synthesis of amines uses potassium phthalimide (prepared from the reaction of phthalimide with potassium hydroxide). The structure and preparation of potassium phthalimide is shown in Figure 13-13. The extensive conjugation (resonance) makes the ion very stable. An example of the Gabriel synthesis is in Figure 13-14. (The N2H4 reactant is hydrazine.) The Gabriel synthesis employs an 8, 2 mechanism, so it works best on primary alkyl halides and less well on secondary alkyl halides. It doesn t work on tertiary alkyl halides or aryl halides. 

Alkylation of the silver salt of pyrid-2-ones usually gives exclusive O-alkylation, whereas alkylation of the sodium or potassium salt gives predominantly TV-alkylation, e.g. Scheme 98. However, the course of such reactions is strongly dependent on conditions. Not only is the nature of the metal salt important but also the structure of the halide, the substituents on the pyridone ring and the solvent used (770PP5,70JOC2517,67JOC4040). 

If we take a series of alkali metal halides, all with the rock salt structure, as we replace one metal ion with another, say sodium with potassium, we would expect the metal-halide internuclear distance to change by the same amount each time if the concept of an ion as a hard sphere with a particular radius holds true. Table 1.8 presents the results of this procedure for a range of alkali halides, and the change in internuclear distance on swapping one ion for another is highlighted. 

Recently, catalyst 50 (n > 4) was reported highly active and selective for olefin synthesis from alkyl halides with aqueous sodium or potassium hydroxide without the formation of by-product alcohols 172). The active catalyst structures were suggested to involve self-solvated polymeric alkoxides 173) 52 and/or complexed hydroxides 53. 

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