Document Type
Article
Department/Program
Chemistry
Journal Title
Journal of Physical Chemistry B
Pub Date
3-28-2013
Volume
117
Issue
12
First Page
3323
Abstract
The local solvent acidities (SA scale) of six 6-carbonyl-2-aminonaphthalene derivatives as beta-cyclodextrin complexes in water are determined through fluorescence quenching. The local polarities (E-T(N) scale) are determined through the shift of the emission center-of-mass. The apparent SA values reflect the solvent structure surrounding the guest's carbonyl group, whereas the apparent E-T(N) values reveal the net polarity of the entire guest molecule. Comparison of these values affords greater insight into the structures of the host-guest complexes. Derivatives 1 and 5 show unusually large acidities, indicative of highly exposed carbonyl groups. The remaining compounds give emission intensities pointing to shielded carbonyl groups. In this study, PRODAN and its derivatives are functioning as dual channel sensors of their local environment.
Recommended Citation
Abelt, Christopher J., Local Solvent Acidities in beta-Cyclodextrin Complexes with PRODAN Derivatives (2013). Journal of Physical Chemistry B, 117(12), 3323-3327.
10.1021/jp400765x
DOI
10.1021/jp400765x