Inclusion complex of 2-naphthylamine-6-sulfonate with β-cyclodextrin: Intramolecular charge transfer versus hydrogen bonding effects
Ayman Abdel-Shafi;
Abstract
The photophysical characteristics of the ground and excited states of 2-naphthylamine-6-sulfonate (2-NA-6-S) were investigated in different solvents and in β-cyclodextrin (β-CD). The spectral shifts are well correlated with Kamlet-Taft relationship. Multiple linear regression analysis indicated that both non-specific dipolar interaction and specific hydrogen bonding interactions play competitive roles in determining the position of the absorption maximum, while the dipolar interaction is the dominating parameter in determining the emission maximum. For the Stokes shift, both the nonspecific interaction and the hydrogen donation property of the solvent are participating equally. The molecular encapsulation of 2-NA-6-S by β-CD in aqueous solution has been studied by different spectroscopic techniques. Fluorescence measurements show that the dielectric constant of β-CD experienced by the included 2-NA-6-S is intermediate between water and methanol. The changes observed in the absorption and fluorescence spectra of 2-NA-6-S upon inclusion in β-CD allowed the association constant to be calculated and found to be 465 ± 100 and 495 ± 100 M-1, respectively. The changes observed for the chemical shifts of 2-NA-6-S and β-CD1H NMR spectra and the corresponding1H NMR spectra of their mixture confirmed the formation of the inclusion complex and showed that 2-NA-6-S is encapsulated in β-CD cavity in a tilted equatorial approach. © 2006 Elsevier B.V. All rights reserved.
Other data
Title | Inclusion complex of 2-naphthylamine-6-sulfonate with β-cyclodextrin: Intramolecular charge transfer versus hydrogen bonding effects | Authors | Ayman Abdel-Shafi | Issue Date | 1-Apr-2007 | Journal | Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy | DOI | 4-5 https://api.elsevier.com/content/abstract/scopus_id/33847266204 1228 66 10.1016/j.saa.2006.06.011 |
PubMed ID | 66 | Scopus ID | 2-s2.0-33847266204 |
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