NMR, relaxometric, and structural studies of the hydration and exchange dynamics of cationic lanthanide complexes of macrocyclic tetraamide ligands

The solution structure and dynamics of metal-bound water exchange have been investigated in a series of lanthanide complexes of primary, secondary, an d tertiary tetraamide derivatives of 1,4,7,10-tetraazacyclododecane. In the gadolinium complexes at ambient pH, water exchange lifetimes (tau(m)) dete rmined by O-17 NMR were sufficiently long (19 mu s for [Gd . 2](3+), 298 K, 17 mu s for [Gd . 3](3+), and 8 mu s for [Gd . 4](3+)) to limit the measur ed relaxivity. Direct H-1 NMR observation of the bound water resonance is p ossible for the corresponding Eu complexes at low temperature in CD3CN, and the rate of water proton exchange is about 50 times faster in the twisted square antiprismatic isomer (m) than in the isomeric square antiprismatic ( M) complex. The ratio of these two isomers in solution is sensitive to the steric demand of the amide substituent, with m/M = 2 for [Eu . 4](3+), but 0.25 for [Eu . 2](3+). The slowness of coordinated water exchange has allow ed the rate of prototropic exchange to be studied: in basic media deprotona tion of the bound water molecule or of proximate ligand amide NH protons le ads to relaxivity enhancements, whereas in acidic media, hydration around t he strongly ion-paired complexes is perturbed, facilitating water exchange. The X-ray crystal structure of ligand 3 reveals a hydrogen-bonded structur e with two pairs of ring N-substituents related in a trans arrangement, con trasting with the structure of diprotonated DOTA in which the ligand is pre disposed to bind metal ions, In the dysprosium complex [Dy . 3 . OH2](PF6)( 3), the metal ion adopts a regular monocapped square antiprismatic coordina tion geometry, with a water Dy-O bond length of 2.427(3) Angstrom, and a PF 6 counterion is strongly hydrogen-bonded to this bound water molecule.