Conductivity study of association of K2Mg[Fe(CN)6], K2Ca[Fe(CN)6] and K2Ba[Fe(CN)6] in aqueous solutions

1980 ◽  
Vol 45 (10) ◽  
pp. 2632-2636
Author(s):  
Alois Fidler ◽  
Jiří Čeleda

The stability constants, Kp0, of ion pairs M2+.[Fe(CN)6]4- and their equivalent conductivities, λp0, at infinite dilution were evaluated by means of two-parameter fitting from the conductivities measured in very diluted aqueous solutions of double hexacyanoferrates of the type K2M(II).[Fe(CN)6] at 25 °C with the use of the limiting Debye-Huckel formula for ionic activity coefficients and Onsager limiting formula for the conductivity of strong electrolytes extended to electrolyte mixtures. Thus, Kp0 = 0.66, 0.72, and 0.76 . 104 dm3/mol and λp0 = 46, 49, and 53 S cm2 /val, respectively.

1977 ◽  
Vol 55 (14) ◽  
pp. 2613-2619 ◽  
Author(s):  
M. S. El-Ezaby ◽  
M. A. El-Dessouky ◽  
N. M. Shuaib

The interactions of Ni(II) and Co(II) with 2-pyridinecarboxaldehyde have been investigated in aqueous solutions at μ = 0.10 M (KNO3) at 30 °C. The stability constants of different complex equilibria have been determined using potentiometric methods. Spectrophotometric methods were also used in the case of the nickel(II) – 2-pyridinecarboxaldehyde system. It was concluded that nickel(II) and cobalt(II), analogous to copper(II), enhance hyrdation of 2-pyridinecarboxaldehyde prior to deprotonation of one of the geminal hydroxy groups. Complex species of 1:1 as well as 1:2 metal ion to ligand composition exist under the experimental conditions used.


1974 ◽  
Vol 13 (6) ◽  
pp. 1434-1437 ◽  
Author(s):  
Sidney. Gifford ◽  
Wayne. Cherry ◽  
Joe. Jecmen ◽  
Mike. Readnour

2016 ◽  
Vol 45 (30) ◽  
pp. 11968-11975 ◽  
Author(s):  
Phuong V. Dau ◽  
Zhicheng Zhang ◽  
Phuong D. Dau ◽  
John K. Gibson ◽  
Linfeng Rao

Three amine-functionalized diamide ligands form tridentate complexes with Nd3+ in aqueous solutions. The stability constants of the complexes follow the order of the ligand basicity that can be tuned by different substitutional groups.


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