Complexes trans-H(6)do2a2p (H6L)with transition metal and lanthanide(III) ions were investigated. Values of stability constants complexes are intermediate in the ligand series as a consequence of this ligand basicity.
The solid-state structures of the ligand and nine lanthanide(III) complexes were determined by X-ray diffraction. The formation kinetics and the acid-assisted dissociation of several Ln(III)-H6L complexes were investigated.
According to the (1)H NMR pseudo-contact shifts for the Ce-Eu and Tb-Yb series, the solution structures of the complexes reflect the structures of the [Ce(HL)(H2O)]2- and [Yb(HL)]2- anions, respectively, found in the solid state. However, these solution NMR studies showed that there is no unambiguous relation between (31)P/(1)H lanthanide induced shift (LIS) values and coordination of water in the complexes.