Use of NMR binding interaction mapping techniques to examine interactions of chiral molecules with molecular micelles
NMR spectroscopy was used to investigate the association of four chiral molecules with the molecular micelle poly(sodium N-undecanoyl-L-leucylvalinate) (poly(SULV)). Adding poly(SULV) to the background electrolyte in electrokinetic chromatography (EKC) allows enantiomeric resolution to be achieved because enantiomers interact differentially with the chiral centers on the micelle headgroups as they both move in the electric field. Pulsed field gradient diffusion experiments were used to measure molecular micelle association constants for enantiomers of each analyte. These association constants were consistent with EKC elution order for the compounds 1,1′-binaphthyl-2,2′-diyl hydrogen phosphate (BNP), 1,1′-bi-2-naphthol (BOH), and Troger's base. In addition, nuclear Overhauser enhancement spectroscopy, nuclear Overhauser effect difference, and intermolecular cross relaxation diffusion experiments were used to generate binding interaction maps for each chiral analyte. These maps showed that BNP and BOH inserted into the surfactant headgroup's major chiral groove and interacted predominately with the leucine chiral center. (+)-Troger's base was also found to insert into the major chiral groove. However, this compound instead interacted with the valine chiral atom. In diffusion experiments with long diffusion times, the linearized diffusion plots for each analyte-molecular micelle mixture showed curvature characteristic of intermolecular cross relaxation. The magnitude of this effect scaled linearly with the analytes' free energies of binding. © 2006 American Chemical Society.
Publication Source (Journal or Book title)
Journal of Physical Chemistry B
Morris, K., Becker, B., Valle, B., Warner, I., & Larive, C. (2006). Use of NMR binding interaction mapping techniques to examine interactions of chiral molecules with molecular micelles. Journal of Physical Chemistry B, 110 (35), 17359-17369. https://doi.org/10.1021/jp0627224