Abstract
Temperature-jump visible spectrophotometric studies show the dye pyronine B (PB) in its monovalent cationic form to be included by γ-cyclodextrin (γCD) in a fast step to form a 1:1 complex (PB·γCD), which is followed by the slower formation of the 2:1 complex (PB)2·γCD, in which pyronine B dimerises: PB +gamma;CD [graphic omitted] PB·gamma;CD (K1)(fast)(1), PB + PB·γCD [graphic omitted] (PB)2·γCD (K2)(slow)(2) where, in aqueous 1.00 mol dm–3 NaCl at pH 5.70 and 298.2 K, K1=(4.3 ± 0.1)× 102 dm3 mol–1, K2=(1.28 ± 0.04)× 105 dm3 mol–1, k2=(8.2 ± 0.2)× 108 dm3 mol–1 s–1 and k–2=(6.40 ± 0.05)× 103 s–1. In the presence of βCD only the formation of PB·βCD is detected and is characterised by k1=(1.1 ± 0.1)× 108 dm3 mol–1 s–1 and k–1=(1.5 ± 0.5)× 104 s–1. Equilibrium u.v.–visible spectrophotometric measurements are consistent with these kinetic data. No inclusion of PB by αCD was detected. These data are compared with those characterising related systems. The dimerisation of PB in the absence of γCD is fast, an observation which forms the basis for some of the mechanistic deductions concerning the formation of (PB)2·γCD, and also for a reassessment of some mechanistic interpretion in earlier studies.
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More From: Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases
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