Enthalpies of transfer of alkane solutes from the vapor state to organic solvents

1985 ◽  
Vol 63 (2) ◽  
pp. 349-352 ◽  
Author(s):  
Richard Fuchs ◽  
W. Kirk Stephenson

Heats of solution of 5 – 8 C5–C16 alkane liquids have been determined in each of 19 organic solvents covering the Taft–Kamlert π* (dipolarity-polarizability) range −0.08 to 1.00. Enthalpies of alkane transfer from vapor to solvents have been calculated (ΔH(v → S) = ΔHs − ΔHv). The methylene increments in (ΔH(v → S) in the 19 solvents and water (−1.18 to −0.67 kcal/mol) are not well correlated with the Hildebrand solubility parameter δ, but an empirical correlation exists with solvent π* and polarizability:[Formula: see text](n = 20, r = 0.977, see = 0.032). By this criterion the small methylene increment in water appears to be associated with the high dipolarity and low polarizability of water.

1985 ◽  
Vol 63 (6) ◽  
pp. 1228-1232 ◽  
Author(s):  
Robert L. Benoit ◽  
Danielle Boulet ◽  
Luc Séguin ◽  
Monique Fréchette

The ionization constants of the conjugated acids BH+ of purine, adenine, 9-methyladenine, adenosine, guanine, and hypoxanthine, and of the related compounds imidazole, N-methylimidazole, benzimidazole, and 4-amino-2,6-dimethylpyrimidine have been determined potentiometrically in Me2SO. The heats of solution and the heats of protonation of most of these bases have been obtained by calorimetry. Some additional determinations were carried out in water so that thermodynamic data in Me2SO and in water could be compared. Our discussion of the solvent effect on these data is largely based on a consideration of the enthalpies of transfer of B and BH+ and emphasizes the contrasting H-bonding properties of the solvents and of the functional groups on the solutes B and BH+.


2008 ◽  
Vol 27 (7) ◽  
pp. 841-849 ◽  
Author(s):  
James E. Code ◽  
Andrew J. Holder ◽  
J. David Eick

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