scholarly journals Study of Acidity Constants of 3-, 4-, 5-, and 6-Chloro-o-toluidinium Ions in Aqueous Solution and Related Thermodynamic Quantities. I

1971 ◽  
Vol 44 (2) ◽  
pp. 455-459 ◽  
Author(s):  
A. H. Gandhi ◽  
S. R. Patel
1988 ◽  
Vol 17 (9) ◽  
pp. 841-863 ◽  
Author(s):  
J. L. Oscarson ◽  
R. M. Izatt ◽  
P. R. Brown ◽  
Z. Pawlak ◽  
S. E. Gillespie ◽  
...  

1980 ◽  
Vol 35 (9) ◽  
pp. 1096-1103 ◽  
Author(s):  
Matthias Kretschmer ◽  
Lutwin Labouvie ◽  
Karl-W. Quirin ◽  
Helmut Wiehn ◽  
Ludwig Heck

Acidity constants of ammine complexes of tetravalent platinum in aqueous solutions have been determined by a spectrophotometric method at very low ionic strengths and extrapolated to zero ionic strength. Temperature variations of pK-values (25 °C and 50 °C) yield thermodynamic parameters for two successive deprotonation steps of hexaammineplatinum(IV), pentaamminechloroplatinum(IV), and tris(ethylenediamine)pla- tinum(IV) complexes and for the deprotonation of pentaammineaquacobalt(III) ion.The enthalpy changes for the first and second steps are similar and range from 50 to 75 kJ/mole while for the aqua ligand of Co(III) 33 kJ/mole are found. The very large dif­ference in the entropy changes (about 70 to 80 J/K mole for the first step and -10 to + 20 J/K mole for the second step) is interpreted by a model of solvation change. The primary hydration sphere of strongly oriented and immobilized water dipoles around the highly charged complex cation is transformed to a hydrogen-bonded solvation sheath when the electric field of the complex is weakened upon release of the first proton.


1992 ◽  
Vol 21 (8) ◽  
pp. 789-801 ◽  
Author(s):  
J. L. Oscarson ◽  
S. E. Gillespie ◽  
R. M. Izatt ◽  
X. Chen ◽  
C. Pando

RSC Advances ◽  
2014 ◽  
Vol 4 (10) ◽  
pp. 5206 ◽  
Author(s):  
Mostafa Abedi ◽  
Hossein Farrokhpour ◽  
Solaleh Farnia

1979 ◽  
Vol 32 (4) ◽  
pp. 709 ◽  
Author(s):  
R Aruga

Heats and entropies of complex formation of the thiophen-2-carboxylate ion with Ni2+, Cu2+, Zn2+ and Cd2+ have been determined by direct calorimetry, the formation constants being known from the literature. The measurements were carried out in aqueous medium at 25�C and an ionic strength of 1. The values of the thermodynamic quantities for thiophen-2-carboxylate, compared with those for (ethylthio)acetate and (phenylthio)acetate obtained previously, indicate a greater tendency for aromatic sulfur to form bonds with the above metals than for aliphatic sulfur. The causes of this behaviour are discussed.


1988 ◽  
Vol 17 (9) ◽  
pp. 865-885 ◽  
Author(s):  
J. L. Oscarson ◽  
S. E. Gillespie ◽  
J. J. Christensen ◽  
R. M. Izatt ◽  
P. R. Brown

2011 ◽  
Vol 42 (3) ◽  
pp. 505-511 ◽  
Author(s):  
M. A. Elbagerma ◽  
H. G. M. Edwards ◽  
Gholamhassan Azimi ◽  
I. J. Scowen

Author(s):  
Margarita Bernabé-Pineda ◽  
Marı́a Teresa Ramı́rez-Silva ◽  
Mario Romero-Romo ◽  
Enrique González-Vergara ◽  
Alberto Rojas-Hernández

2013 ◽  
Vol 42 (15) ◽  
pp. 5566 ◽  
Author(s):  
Mostafa Abedi ◽  
Hossein Farrokhpour

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