Abstract
Abstract Guest binding ability of N-(l-pyrenecarbonyl)-3A-amino-3A-deoxy-(2AS,3AS)-γ-cyclodextrin (1) was evaluated by its fluorescence intensity variation induced by guest, and compared with that of primary hydroxyl side modified analogue (2). The results showed that 1 was an extremely better host than 2 in binding guest, promising that the secondary hydroxyl side modified CDs can become useful molecular recognition sensory systems.
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