Abstract
A series of new calixarene-based fluoroionophores were synthesized. With our new calixarene derivative bearing a crown ether and an azacrown ether as two binding sites, the metal ion was found to selectively choose its better binding pocket between these two ligands. Interesting "molecular taekowndo" processes between Ag+-K+, Cu2+-K+, and Ag+-Cs+ pairs were easily monitored via fluorescence change.
| Original language | English |
|---|---|
| Pages (from-to) | 2348-2351 |
| Number of pages | 4 |
| Journal | Journal of Organic Chemistry |
| Volume | 67 |
| Issue number | 7 |
| DOIs | |
| State | Published - 5 Apr 2002 |
Fingerprint
Dive into the research topics of 'Pyrene-armed calix[4]azacrowns as new fluorescent ionophores: "Molecular taekowndo" process via fluorescence change'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver