Manipulating Photochemical Reactivity of Coumarins within Cucurbituril Nanocavities
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 func...
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Veröffentlicht in: | Organic letters 2008-08, Vol.10 (15), p.3339-3342 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | 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. |
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ISSN: | 1523-7060 1523-7052 |
DOI: | 10.1021/ol801256r |