Solution Properties of Tetraalkylammonium Halide and Alkali-Metal Halide Ion Pairs. The Relationship Between Dissociation Constants and Solubility Products

1987 ◽  
Vol 40 (7) ◽  
pp. 1201 ◽  
Author(s):  
W Mizerski ◽  
MK Kalinowski

An empirical relation describing the effect of solvent on the dissociation constant ( Kd ) of ion pairs is described. An equation of the form pKd = apKso + bD-1 + c ( Kso and D stand for the solubility product of a given salt and for the electric permittivity of a solvent, respectively) has been tested with 13 sets of experimental data for salts containing tetraalkylammonium and alkali-metal cations. A successful correlation was obtained in 100% of the cases considered.

1974 ◽  
Vol 52 (18) ◽  
pp. 3259-3268 ◽  
Author(s):  
G. A. Salmon ◽  
W. A. Seddon ◽  
J. W. Fletcher

Pulse radiolysis of solutions of alkali metal cations in tetrahydrofuran (THF) demonstrates the formation of solvated electrons es−, alkali metal cation-ion pairs (M+, es−), and alkali metal anions M−. This paper describes the spectra, extinction coefficients, and radiolytic yields of es−, lithium, sodium, potassium, and cesium species in THF. The reaction kinetics are complex but largely involve reactions A and B[Formula: see text]with the concomitant disappearance of all three species by reaction with radiolytically produced radicals. Rate constants and ion-pair dissociation constants for es− and the sodium and potassium species are presented and compared with data established from studies of blue solutions of alkali metals dissolved in THF.


1967 ◽  
Vol 45 (20) ◽  
pp. 2411-2418 ◽  
Author(s):  
R. W. Chlebek ◽  
M. W. Lister

The rates of the reaction of ferrocyanide and persulfate ions, in the presence of various concentrations of different alkali metal cations, have been measured at various temperatures and ionic strengths. The results are interpreted in terms of ion pairs and support the view that the actual reacting species are MFe(CN)6−3 and MS2O8−, where M is an alkali metal. This is similar to the situation found earlier for potassium salts of these ions. The rate constants obtained on this assumption increase gradually from lithium to cesium. Values are also obtained for the apparent activation energies of these reactions.


1967 ◽  
Vol 40 (6) ◽  
pp. 1325-1332 ◽  
Author(s):  
Masamoto Iwaizumi ◽  
Masayasu Suzuki ◽  
Taro Isobe ◽  
Hiroshi Azumi

1971 ◽  
Vol 49 (9) ◽  
pp. 1377-1383 ◽  
Author(s):  
Richard H. Cox

The 1H n.m.r. spectra of carbazole nitranion, 4,5-methylene- and 9,10-dihydro-4,5-methylene-phenanthrene carbanions with various alkali metal cations have been analyzed in terms of chemical shifts and coupling constants. Chemical shifts of the anions depend upon cation and solvent and are related to the type of ion pairs present. The 7Li n.m.r. data indicate that Li is associated with the nitrogen of carbazole nitranion whereas with the 4,5-methylenephenanthrene carbanions, Li appears to be located in the π-cloud of the anions and associated equally with all carbons in the anion. The results are discussed in terms of the types of ion pairs present and the association of cation with anion.


ChemInform ◽  
1989 ◽  
Vol 20 (7) ◽  
Author(s):  
M. BARZAGHI ◽  
A. GAMBA ◽  
C. OLIVA ◽  
M. BRANCA ◽  
A. SABA

1987 ◽  
Vol 111 ◽  
Author(s):  
Alon V. McCormick ◽  
A. T. Bell ◽  
C. J. Radke

AbstractBy means of 29Si spectroscopy, it is established that the distribution of silicate anions in alkaline silicate solutions is a moderate function of base composition. At a fixed SiO2. concentration and silicate ratio, the proportion of Si present in oligomeric and cage-like structures increases in progressing from Li to Cs hydroxide. Interactions between alkali metal cations and silicate anions are investigated using NMR spectroscopy of the cations; in this way the concentration of ion pairs is measured as a function of cation size. As a result the silicate redistribution is ascribed to cation-silicate anion pairing and to a higher selectivity for ion pairing by large silicate anions as cation size increases.


1972 ◽  
Vol 12 (4) ◽  
pp. 596-598 ◽  
Author(s):  
J. van der Kooij ◽  
N.H. Velthorst ◽  
C. MacLean

Sign in / Sign up

Export Citation Format

Share Document