Abstract
The interaction between β-cyclodextrin (β-CD) and riboflavin together with its electrogenerated intermediate anion radicals has been specifically investigated by in situ electrochemical UV-visible spectroscopy. It appears that the anion radicals are included more tightly than the parents and stabilized in the special microenvironment of the β-CD cavity. The utility of β-CD for probing the existence of an unstable intermediate species at the electrode is also demonstrated.
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