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HERO ID
8431991
Reference Type
Journal Article
Title
1002. The stability of metal complexes of 1,10-phenanthroline and its analogues. Part I. 1,10-Phenanthroline and 2,2â²-bipyridyl
Author(s)
Irving, H; Mellor, DH
Year
1962
Is Peer Reviewed?
Yes
Journal
Journal of the Chemical Society
ISSN:
0368-1769
Page Numbers
5222-5237
Language
English
DOI
10.1039/JR9620005222
Abstract
Methods suitable for determining the step-stability constants of very stable complexes of transition metals with 1,10-phenanthroline and its analogues are reviewed. Partition coefficients for 2,2â²-bipyridyl and 1,10-phenanthroline between aqueous buffers of ionic strength 0.1M and chloroform, carbon tetrachloride, and n-hexane have been measured at 25°. From measurements of the distribution of the two ligand bases between these solvents and aqueous buffers containing known concentrations of various cations, step-stability constants, valid for 25° and 0.1M-potassium chloride (or nitrate) have been determined for bivalent ions of manganese, iron, cobalt, nickel, copper, zinc, and cadmium. The stabilities of the 1:1 complexes follow the Irving-Williams order in each case and they increase in the order Mn<Cd<Fe<Zn<Co<Ni<Cu. For the 3:1 complexes, however, the order becomes Mn<Cd<Zn<Co<Cu<Fe<Ni. The anomalous stability of the ferrous tris-complex is shown to arise because K3 is greater than both K1 and K2, owing to formation of a spin-paired complex.
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