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. Author manuscript; available in PMC: 2009 Sep 23.
Published in final edited form as: Chemistry. 2008;14(9):2658–2667. doi: 10.1002/chem.200701747

Figure 1.

Figure 1

The up-field region of the 1H NMR spectra of [Tb(S-SSSS-1)(D2O)] recorded at 295.2 K in D2O 200 MHz (bottom) and of [Tb(S-RRRR-1)(D2O)] recorded 332.7 K in D2O at 200 MHz (top). The down-field regions of the spectra are not displayed owing to the limited bandwidth of the excitation pulse. The assignments of the protons of the macrocyclic ring are shown in which axS refers to the axial proton of the carbons located on the side of the ring and eqS, the equatorial proton of the same carbon. eqC refers to the equatorial proton located on the carbon located on the corner of the ring.[25] Molecular models of the complexes are also shown, illustrating the difference in coordination geometry between two stereoisomers.[26]