Abstract

For the title systems, single crystal X-ray data indicate the presence of totally asymmetric structures. These features are reflected in the multiplicity of resonances in the solid phase 13C NMR spectra. Some of the 13C chemical shift trends are analyzed in terms of torsional angle influences. In solution, resonance assignments have been made with the aid of 2D methods. Stereochemical inferences are drawn from NOESY spectra and 1H–1H couplings. Low temperature solution experiments indicate that conformational interconversions in both the free ligand and the NaNCS complex are rapid on the NMR timescale down to 163 K. Key words: crown ethers, NMR, stereochemistry.

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