jo047841z_si_001.pdf (3.22 MB)

Anthryl-Substituted Heterocycles as Acid-Sensitive Fluorescence Probes

Download (3.22 MB)
journal contribution
posted on 13.05.2005, 00:00 by Heiko Ihmels, Andreas Meiswinkel, Christian J. Mohrschladt, Daniela Otto, Michael Waidelich, Michael Towler, Rick White, Martin Albrecht, Alexander Schnurpfeil
Four pH-sensitive fluorescence probes are presented which consist of an anthracene fluorophore and a π-conjugated oxazoline, benzoxazole, or pyridine substituent. The protonation of the heterocycles increases their acceptor properties and results in significant red-shifts of the absorption and emission maxima of the anthracene chromophore. The comparison between 2-[2‘-(6‘-methoxyanthryl)]-4,4-dimethyl-2-oxazoline and 2-[2‘-(anthryl)]-4,4-dimethyl-2-oxazoline reveals that the donor−acceptor substitution pattern of the fluorophore is not required to achieve a red shift upon protonation. The benzoxazole and pyridine substituents offer a particular advantage due to their persistence under acidic conditions. Thus, these compounds may be used as efficient pH-sensitive fluorescence switches. Nevertheless, the switching of benzoxazole 2c requires relatively strong acidic conditions. The anthrylpyridinium exhibits a red-shifted emission in chloroform; however, it is nonfluorescent in aqueous or alcoholic solution. Although the oxazoline is not persistent under permanent acidic conditions, this heterocycle may be useful as a substituent in fluorescence indicators since it may be used to detect acid concentrations of 10-4−10-5 M, which are close to the biologically relevant range.

History

Exports