Partial Molar Enthalpy of Solution for Tris(2,4-pentanedionato)cobalt(III) in Mixed Solvents of Water and Dimethyl Sulfoxide

1986 ◽  
Vol 59 (7) ◽  
pp. 2135-2140 ◽  
Author(s):  
Yasuki Yoshimura ◽  
Nobuyoshi Sato ◽  
Makoto Kikuchi
1988 ◽  
Vol 66 (4) ◽  
pp. 637-644 ◽  
Author(s):  
Dian-Yuan Men ◽  
Jia-Zhen Yang ◽  
Chun-Yu Liang ◽  
Li-Tian Zhang ◽  
Huan Gao ◽  
...  

This paper reports electromotive force measurements of the cells[Formula: see text]and[Formula: see text]in mixed solvents of urea, mole fraction x = 0.05, at five temperatures from 278.15 to 318.15 K. The standard potentials of Ag–AgCl electrode in mixed solvents were obtained from the emf of cell (A) for HCl of molality mA from 0.02 to 0.11 mol kg−1, both by extrapolation on the basis of an extended Debye–Hückel equation and by a polynomial approach proposed in this paper on the basis of Pitzer's electrolytic solution theory. The standard free energies of transfer for HCl are discussed. The activity coefficients of HClγA in HCl + NaCl + urea + water have also been obtained from the emf of cell (B) at constant total ionic strength I = 0.5, 1.0, 1.5, and 2.0 mol kg−1. The experimental results show that HCl obeys Harned's rule and log γA is a linear function of absolute temperature T. They also indicate that the relative partial molar enthalpy of HCl obeys a similar Harned's rule.


Polymer ◽  
2003 ◽  
Vol 44 (15) ◽  
pp. 4075-4078 ◽  
Author(s):  
Nobuaki Takahashi ◽  
Toshiji Kanaya ◽  
Koji Nishida ◽  
Keisuke Kaji

1983 ◽  
Vol 36 (10) ◽  
pp. 1923 ◽  
Author(s):  
JMB Harrowfield ◽  
L Spiccia ◽  
DW Watts

Previous work on the reduction of a series of cobalt(III) complexes by iron(II) in dipolar aprotic solvents and in aqueous mixtures has been extended to reduction by copper(I). The greater stability of copper(I) to disproportionation in these media has permitted the study of the reduction of CoF(NH3)52+ and Co(HCOO)(NH3)52+ in range of solvents over a number of temperatures with a precision not possible in previous studies in water. The results are consistent with an inner-sphere mechanism in which the copper(I) reductant is preferentially solvated by dimethyl sulfoxide to the exclusion of water in mixed solvents.


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