The capacity of a new ligand, 2-(hydroxyimino)propanohydroxamic acid (HPH,
an analog of alanine), to bind the Al3+ ion has been examined. A particular
objective was to check whether the HPH oximic group could take part in alu
minum co-ordination together with the two hydroxamic oxygens, a possibility
that could make HPH an efficient low-molecular-mass ligand for detrimental
Al3+ ions in vivo. Glass electrode potentiometry, NMR spectroscopy and Ele
ctrospray Mass Spectrometry were used to investigate Al3+-HPH complex equil
ibria and their related structural aspects. The aluminium binding capacity
of HPH was compared to that of other monohydroxamic acids. In spite of the
lowest basicity of its hydroxamic moiety and the non-involvement of its oxi
mic moiety in metal ion binding, HPH was found to be a very competitive lig
and. Comparative quantum calculations performed on the systems involved sug
gest that electrostatic interactions induced by the ligand molecule are det
ermining for complex stability.