scholarly journals Studies on New Derivatives of 8-Quinolinol as Chelating Agents. I. Syntheses, Coloration Reaction with Metal Ions and Acid Dissociation Constants of Some Azomethine and Aminomethyl Derivatives

1972 ◽  
Vol 45 (2) ◽  
pp. 477-481 ◽  
Author(s):  
Takehisa Hata ◽  
Toyozo Uno
1965 ◽  
Vol 43 (1) ◽  
pp. 64-74 ◽  
Author(s):  
T. L. Meek ◽  
G. E. Cheney

A survey has been made of the reactions of both geometric isomers of phenyl-2-pyridyl ketoxime with metal ions. The complexes of copper(II) with the syn-phenyl isomer have been investigated. Acid dissociation constants of both geometric isomers, and of the 2:1 copper chelate of the syn-phenyl oxime have been determined.


1966 ◽  
Vol 19 (11) ◽  
pp. 2035 ◽  
Author(s):  
SHH Chaston ◽  
SE Livingstone

The acid dissociation constants (PKD) of the monothio derivatives of acetyl-acetone, dibenzoylmethane, and 3,3,3-trifluoro-1-(2- thenoyl)acetone, viz. 4-mercap-topent-3-en-2-one (I), 3-mercapto-1,3- diphenylprop-2-en-1-one (II), and 1,1,1-trifluoro-4-mercapto-4-(2- thienyl)but-3-en-2-one (III), were determined in dioxan/water solutions with varying mole fraction (n2) of dioxan. Over a range of n2 from 0.18 to 0.44 the values of pKD were found to vary linearly with n2 as given by the equations: (I) pKD = 5.7+12.0n2; (II) pKD = 7.0+10.9n2; (III) pKD = 3.55 + 9.2n2. The thio derivatives (I), (II), and (III) have pKD values 2.0-2.7 log units lower than their oxygen analogues. The logarithm of the stability constants (log β2) for the nickel(II) and copper(II) complexes of (II) were found to be 21.7 and 22.2, respectively. For both complexes K2 > K1. Comparison with the stability constants of the dibenzoylmethane complexes shows that for nickel(II) the complex of the monothio-β-diketone is more stable than that of the β-diketone while the converse is true for copper(II).


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