Asymmetric ruthenium(II) complexes of a flexible aminomethylpyridine derivative exhibit diastereotopic ligand methylene protons, as measured by NMR spectroscopy; binding of external anions renders these protons equivalent possibly by increasing dynamically averaged symmetry; the amount of anion needed to raise average symmetry correlates to the anion binding constant.
S. J. Dickson, S. C. G. Biagini and J. W. Steed, Chem. Commun., 2007, 4955 DOI: 10.1039/B712699A
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