Coumarin derivatives that are either cationic (7-ammonium) or neutral (7-hydroxy, 7-methoxy, 6-methyl) form a 1:2 host-guest complex with cucurbit[8]uril (CB[8]). Direct irradiation of these coumarin@CB[8] complexes in water gives head-to-tail (HT) adduct as the major product. The nature of the functional group (polar or nonpolar) at the 6 or 7 position on the coumarin dictates the type of HT adduct ( syn- or anti-). It is postulated that the available free volume and the hydrophobic confined environment are responsible for the observed selectivity.
No takes yet. Share an insight, caveat, or question.
Barooah et al. (2008) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: