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. 2016 Jan 15;7(4):2592–2603. doi: 10.1039/c5sc04805b

Fig. 7. 1H NMR spectrum (499.9 MHz, 293 K, CDCl3) of rotaxane trans-R together with selected proton assignments. Resonances arising from the protons on the isoxazolidine ring are highlighted in purple. Resonances arising from the magnetically-inequivalent pyridine protons (red), NH (blue) and methylene protons (orange) located on the macrocycle, are shown as partial inset spectra. The sample also contains around 5% of cis-R.

Fig. 7