| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1306483 | Inorganic Chemistry Communications | 2008 | 6 Pages |
Two novel calix[4]arene–Schiff base receptors have been synthesized. One of the new compounds has two pendant aldimines, while the second has been prepared by two-point attachment of a calixarene–dialdehyde onto a calixarene–diamine to form a “calix-tube”. Preliminary binding studies with AgClO4 show large complexation-induced shifts in 1H NMR positions.
Graphical abstractTwo novel calix[4]arene–Schiff base receptors have been synthesized. One of the new compounds has two pendant aldimines, while the second has been prepared by two-point attachment of a calixarene–dialdehyde onto a calixarene–diamine to form a “calix-tube”. Preliminary binding studies with AgClO4 show large complexation-induced shifts in 1H NMR positions.Figure optionsDownload full-size imageDownload as PowerPoint slide
