Abstract
This work focuses on the inclusion complexes of γ-cyclodextrin and pyrene as indicated by fluorescence lifetime analyses and the influences of chiral alcohols and diols on these complexes. The 2-butanol participates in the γ-cyclodextrin-pyrene complexation and produces a longer lifetime of complexed pyrene than the value determined for the complex in pure water. The enantiomeric 1,3-butanediol also produces a longer lifetime of complexed pyrene. However, a decrease in this lifetime is observed in the presence of racemic 1,3-butanediol. This study also involves an estimation of formation constants for γ-cyclodextrin-pyrene complexes by use of the fluorescence lifetime measurements.
PDF Article
More Like This
Studying biological tissue with fluorescence lifetime imaging: microscopy, endoscopy, and complex decay profiles
Jan Siegel, Daniel S. Elson, Stephen E. D. Webb, K. C. Benny Lee, Alexis Vlandas, Giovanni L. Gambaruto, Sandrine Lévêque-Fort, M. John Lever, Paul J. Tadrous, Gordon W. H. Stamp, Andrew L. Wallace, Ann Sandison, Tim F. Watson, Fernando Alvarez, and Paul M. W. French
Appl. Opt. 42(16) 2995-3004 (2003)
Cited By
You do not have subscription access to this journal. Cited by links are available to subscribers only. You may subscribe either as an Optica member, or as an authorized user of your institution.
Contact your librarian or system administrator
or
Login to access Optica Member Subscription