Solubility group 2 halides

A special role in the chemistry of nickel and cobalt alkoxide derivatives is played by the poorly soluble methoxide halids studied in detail by the group of Winter [964, 865]. According to the diffuse reflectance spectra, the coordina-... 

Barium is a member of the alkaline-earth group of elements in Group 2 (IIA) of the period table. Calcium [7440-70-2], Ca, strontium [7440-24-6], Sr, and barium form a closely allied series in which the chemical and physical properties of the elements and their compounds vary systematically with increasing size, the ionic and electropositive nature being greatest for barium (see Calcium and calcium alloys Calcium compounds Strontium and STRONTIUM COMPOUNDS). As size increases, hydration tendencies of the crystalline salts increase solubilities of sulfates, nitrates, chlorides, etc, decrease (except fluorides) solubilities of halides in ethanol decrease thermal stabilities of carbonates, nitrates, and peroxides increase and the rates of reaction of the metals with hydrogen increase. 

Redox Chemistry of the Group 5 Clusters Ligand Substitution Electronic and Molecular Structure Niobium Iodide Clusters NbJJ"-Materials Chemistry Derived from Soluble Metal Halide Clusters A. Higher Nuclearity Clusters Supported Cluster Materials Charge-Transfer Salt Complexes Extended Solids Chemically Modified Surfaces... 

The use of metals from groups III to VIII was patented by Kelly, where he obtained good results with Ti (IV)- and Cr (Ill)-based soluble catalysts at 115°C (Kelly, 1991). Hayashi and Sasaki (2005) have reported the conversion of trioses (eg, DHA and GLY) into alkyl lactates in alcoholic media with the use of soluble Sn halides (Hayashi and Sasaki, 2005). 

Other Group II halides are essentially ionic and therefore have relatively high m.p., the melts acting as conductors, and they are soluble in water but not in organic solvents. 

These are halides formed by highly electropositive elements (for example those of Groups I and II, except for beryllium and lithium). They have ionic lattices, are non-volatile solids, and conduct when molten they are usually soluble in polar solvents in which they produce conducting solutions, indicating the presence of ions. 

The —OH group of phenols makes it possible for them to participate m hydrogen bonding This contributes to the higher boiling points and greater water solubility of phenolic compounds compared with arenes and aryl halides... 

The catalysts used are themselves complexes produced by interaction of alkyls of metals in Groups l-IIl of the Periodic Table with halides and other derivatives of Groups IV-VIII metals. Although soluble co-ordination catalysts are known, those used for the manufacture of stereoregular polymers are usually solid or adsorbed on solid particles. 

Pure NI3 has not been isolated, but the structure of its well-known extremely shock-sensitive adduct with NH3 has been elucidated — a feat of considerable technical virtuosity.Unlike the volatile, soluble, molecular solid NCI3, the involatile, insoluble compound [Nl3.NH3] has a polymeric structure in which tetrahedral NI4 units are comer-linked into infinite chains of -N-I-N-I- (215 and 230 pm) which in turn are linked into sheets by I-I interactions (336 pm) in the c-direction in addition, one I of each NI4 unit is also loosely attached to an NH3 (253 pm) that projects into the space between the sheets of tetra-hedra. The stmcture resembles that of the linked Si04 units in chain metasilicates (p. 349). A further interesting feature is the presence of linear or almost linear N-I-N groupings which suggest the presence of 3-centre, 4-electron bonds (pp. 63, 64) characteristic of polyhalides and xenon halides (pp. 835-8, 897). 

The solubilities of the ionic halides are determined by a variety of factors, especially the lattice enthalpy and enthalpy of hydration. There is a delicate balance between the two factors, with the lattice enthalpy usually being the determining one. Lattice enthalpies decrease from chloride to iodide, so water molecules can more readily separate the ions in the latter. Less ionic halides, such as the silver halides, generally have a much lower solubility, and the trend in solubility is the reverse of the more ionic halides. For the less ionic halides, the covalent character of the bond allows the ion pairs to persist in water. The ions are not easily hydrated, making them less soluble. The polarizability of the halide ions and the covalency of their bonding increases down the group. 

Alternatively, the Sn2 nucleophilic substitution reaction between alcohols (phenols) and organic halides under basic conditions is the classical Williamson ether synthesis. Recently, it was found that water-soluble calix[n]arenes (n = 4, 6, 8) containing trimethylammonium groups on the upper rim (e.g., calix[4]arene 5.2) were inverse phase-transfer catalysts for alkylation of alcohols and phenols with alkyl halides in aqueous NaOH solution to give the corresponding alkylated products in good-to-high yields.56... 

The water-soluble calix[n]arenes 6.3 (n = 4, 6 and 8) containing trimethylammonium groups act as efficient inverse phase-transfer catalysts in the nucleophilic substitution reaction of alkyl and arylalkyl halides with nucleophiles in water (Eq. 6.19).40 In the presence of various surfactants (cationic, zwitterionic and anionic), the reactions of different halides and ketones show that the amount of ketone alkylation is much higher and that the reactions are faster in the presence than in the absence of surfactant aggregates.41 The hydrolysis of the halide is minimized in the presence of cationic or zwitterionic surfactants. 

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