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Rotational correlation times of metal ion aqua complexes can be detd. from 17O NMR relaxation rates if the quadrupole coupling const. of the bound water oxygen-17 nucleus is known. The rotational correlation time is an important parameter for the efficiency of Gd3+ complexes as magnetic resonance imaging contrast agents. Using a combination of d. functional theory with classical and Car-Parrinello mol. dynamics simulations we performed a computational study of the 17O quadrupole coupling consts. in model aqua ions and the [Gd(DOTA)(H2O)]- complex used in clin. diagnostics. For the inner sphere water mol. in the [Gd(DOTA)(H2O)]- complex the detd. quadrupole coupling parameter cÖ1+h2/3 of 8.7 MHz is very similar to that of the liq. water (9.0 MHz). Very close values were also predicted for the the homoleptic aqua ions of Gd3+ and Ca2+. We conclude that the 17O quadrupole coupling parameters of water mols. coordinated to closed shell and lanthanide metal ions are similar to water mols. in the liq. state.
Sara Bonella, Andrea Cavalli, Taylor James Baird