Inclusion Complexes of Cyclodextrins with 4-Amino-1,8-Naphthalimides
Tóm tắt
The formation of inclusion complexes between 4-amino-1,8-naphthalimides and cyclodextrins (CDs) was investigated. The naphthalimides used in the study were 4-amino-1,8-naphthalimide (I) and4-(2-phosphonoethylamino)-N-(2-phosphonoethyl)-1,8-naphthalimide,tetraethylester (II). The CDs employed were α-CD, β-CD, γ-CD, HP-α-CD, HP-β-CD andHP-γ-CD (HP = hydroxypropyl). Evidence for complex formation was obtained from the changes in the fluorescence spectra of the dyes in the presence of increasing amounts of the CDs. The most striking changes were observed with HP-β-CD and HP-γ-CD. Treatment of the data using Benesi–Hildebrand plotswas consistent with a 1:1 inclusion model. The determined stabilityconstants were (Keq, M-1): 106 (I:HP-β-CD, pH = 2.0), 193 (I:HP-β-CD, pH = 7.0), 113 (I:HP-γ-CD, pH = 7.0), 155(II:HP-β-CD, pH = 2.0), 121 (II:HP-β-CD,pH = 7.0), 301 (II:HP-γ-CD, pH = 7.0). It can beconcluded that compound I forms a more stable complex with HP-β-CD than with HP-γ-CD. Compound II, on the other hand, forms a more stable complex with HP-γ-CD than with HP-β-CD.
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