The Mechanisms of Racemization of the 2,2'-Bipyridinebis-(1,10-phenanthroline) nickel(II) Ion and the 1,10-Phenanthrolinebis-(2,2'-bipyridine)-nickel(II) Ion
JA Broomhead and FP Dwyer
Australian Journal of Chemistry
16(1) 51 - 65
Published: 1963
Abstract
The rates of racemization of the 1,10-phenanthrolinebis-(2,2'-bipyridine)nickel(II) ion and the 2,2'-bipyridinebis-(1,10-phenanthroline)nickel(II) ion have been measured in neutral, acid, and basic solutions as well as in organic solvents. Comparison of the rates in acid solution with the corresponding rates of dissociation has shown that racemization takes place by means of an intermolecular mechanism with the loss of one bipyridine ligand. Increased racemization rates in the presence of acids, bases, and specific ions such as NO2-;, Cl-, Br- have been accounted for by the same mechanism.https://doi.org/10.1071/CH9630051
© CSIRO 1963