Abstract
A novel calix[4]arene derivative locked in the 1,3-alternate conformation (2) bearing two pyrene and rhodamine fluorophores was synthesized as a selective sensor for the Hg2+ ion. The sensoring is based on FRET from pyrene excimer emissions to ring-opened rhodamine absorption upon complexation of the Hg2+ ion. Addition of Hg2+ to a mixed solution of 2 gave significantly enhanced fluorescence at ∼576 nm via FRET with excitation at 343 nm. We also found that the pyrene excimer emissions formed by the intramolecular π-π interactions are more effective in obtaining strong FRET bands than those by intermolecular π-π interactions.
Original language | English |
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Pages (from-to) | 7159-7165 |
Number of pages | 7 |
Journal | Journal of Organic Chemistry |
Volume | 75 |
Issue number | 21 |
DOIs | |
Publication status | Published - 2010 Nov 5 |
ASJC Scopus subject areas
- Organic Chemistry