| Literature DB >> 28398613 |
Eszter Boros1, Raja Srinivas2, Hee-Kyung Kim1, Arnold M Raitsimring3, Andrei V Astashkin3, Oleg G Poluektov4, Jens Niklas4, Andrew D Horning2, Bruce Tidor2, Peter Caravan1.
Abstract
Aqua ligands can undergo rapid internal rotation about the M-O bond. For magnetic resonance contrast agents, this rotation results in diminished relaxivity. Herein, we show that an intramolecular hydrogen bond to the aqua ligand can reduce this internal rotation and increase relaxivity. Molecular modeling was used to design a series of four Gd complexes capable of forming an intramolecular H-bond to the coordinated water ligand, and these complexes had anomalously high relaxivities compared to similar complexes lacking a H-bond acceptor. Molecular dynamics simulations supported the formation of a stable intramolecular H-bond, while alternative hypotheses that could explain the higher relaxivity were systematically ruled out. Intramolecular H-bonding represents a useful strategy to limit internal water rotational motion and increase relaxivity of Gd complexes.Entities:
Keywords: aquo-ion dynamics; gadolinium complexes; molecular dynamics; relaxivity
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Year: 2017 PMID: 28398613 PMCID: PMC5558827 DOI: 10.1002/anie.201702274
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336