Tetraethylammonium iodide

Author(s):  
Tse-Lok Ho ◽  
Mary Fieser ◽  
Louis Fieser
1990 ◽  
Vol 19 (6) ◽  
pp. 569-587 ◽  
Author(s):  
Alessandro De Robertis ◽  
Concetta De Stefano ◽  
Carmelo Rigano ◽  
Silvio Sammartano

1968 ◽  
Vol 46 (16) ◽  
pp. 2749-2752 ◽  
Author(s):  
L. Fabes ◽  
J. K. S. Wan

γ-Irradiation of polycrystalline tetraethylammonium iodide at 77°K leads to the breaking of a C—C bond and the primary radicals ĊH3 and [Formula: see text] were detected by electron spin resonance. The methyl radicals were found to disappear readily at 120°K. In the range of 263–273°K a secondary reaction between [Formula: see text] and the parent ion [Formula: see text] was observed; the resulting secondary radical [Formula: see text] was found to be stable up to 373°K.


1968 ◽  
Vol 46 (12) ◽  
pp. 2005-2011 ◽  
Author(s):  
W. A. Adams ◽  
K. J. Laidler

The ion-pair dissociation constants determined from a Shedlovsky analysis of conductivity (see Part I) were used to calculate the enthalpy, the internal energy at constant volume, the entropy, and the volume of dissociation of tetramethylammonium iodide, tetraethylammonium iodide, and tetra-n-propylammonium iodide ion pairs in acetone solution. The sign and magnitude of these parameters over the range of conditions investigated, temperature 25 to 55 °C and atmospheric to 1.1 kbar pressure, indicated that the free ions in acetone solution are extensively solvated and that, depending on the conditions, solvent-shared or solvent-separated ion pairs are formed.


1991 ◽  
Vol 46 (1-2) ◽  
pp. 122-126 ◽  
Author(s):  
E. Hawlicka ◽  
R. Grabowski

AbstractThe conductance of Nal and Et4NI in methanol-acetonitrile and methanol-water mixtures was measured at 25 ± 0.005 °C for the whole range of the solvent compositions, the salt molarity ranging from 5 • 10-5 up to 1 • 10-2. Several equations describing the influence of the salt concentration on the equivalent conductance are examined and the Fuoss-Hsia equation with the Fernandez-Prini parameters is found to be the most appropriate one for systems with weak ionic association. Variations with the solvent composition of the limiting equivalent conductance, the distance between ions forming ion pairs and the association constant are discussed. Nonmonotonous changes of the association constant are concluded to be a feature of microheterogenous systems.


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