Solvent Effect in the Electrochemical Reduction of p‐Quinones in Several Aprotic Solvents

1990 ◽  
Vol 137 (8) ◽  
pp. 2437-2443 ◽  
Author(s):  
Kazuo Sasaki ◽  
Tomoyuki Kashimura ◽  
Masahiro Ohura ◽  
Yasushi Ohsaki ◽  
Nobuaki Ohta
Author(s):  
Silvia Mena ◽  
Esteve Ribas ◽  
Clara Richard ◽  
Iluminada Gallardo ◽  
Jordi Faraudo ◽  
...  

1998 ◽  
Vol 102 (11) ◽  
pp. 2045-2050 ◽  
Author(s):  
Tateki Ishida ◽  
Fumio Hirata ◽  
Hirofumi Sato ◽  
Shigeki Kato

1977 ◽  
Vol 55 (5) ◽  
pp. 792-797 ◽  
Author(s):  
Robert L. Benoit ◽  
Michael F. Wilson ◽  
Sing-Yeung Lam

The solvent effect on the iodide–triiodide equilibrium has been investigated by means of calorimetric and potentiometric measurements. The aprotic solvents studied were nitromethane, nitrobenzene, sulfolane, acetonitrile, propylene carbonate, acetophenone, dimethylformamide, dimethylsulfoxide, and o-dichlorobenzene. The resulting enthalpy and free energy changes imply that the variations of the enthalpies and free energies of transfer of the iodide and triiodide ions probably are small and that there is an important non-coulombic contribution to these transfer parameters. Values were obtained for the enthalpy of formation of two solid triiodides, which together with values for other triiodides, cast doubt on reported calculated lattice enthalpies of triiodides and formation enthalpy of I3− ion in the gas phase. This latter formation enthalpy is found to be, from our solution data, more negative than −22 kcal mol−1.


1980 ◽  
Vol 25 (9) ◽  
pp. 1127-1134 ◽  
Author(s):  
J. Volke ◽  
D. Beyrová ◽  
J. Klíma ◽  
V. Volkeová ◽  
J. Hlavatý ◽  
...  

1973 ◽  
Vol 4 (39) ◽  
pp. no-no
Author(s):  
ROBERT P. MARTIN ◽  
WILLIAM H. JUN. DOUB ◽  
JULIAN L. JUN. ROBERTS ◽  
DONALD T. SAWYER

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