Abstract
A variety of transition
metal complexes of a-amino acid esters have been synthesized, and characterized
by analysis, conductivity measurements, and infrared spectra. The complexes can
be broadly divided into two groups: (a) complexes in which only a metal-nitrogen
bond occurs with the α-amino group of the ester, and (b) complexes in
which chelate ring formation occurs via secondary donor groups on the ligand.
These latter complexes are found with methyl L-histidinate, methyl γ-glutamate,
and methyl L-cysteinate. With the exception of a methyl tryptophanate complex,
the infrared spectra show that there is no interaction between the carbonyl
group of the ester and the metal ion.
The visible spectra of aqueous solutions
of the esters and copper(II) at a ligand/metal ratio of 5 : 1 have maxima in
the 600-650 mμ range at pH 7 consistent with
copper-nitrogen bonding only.
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