Abstract
A novel bis(m-phenylene)-26-crown-8-based lariat ether (i.e., 3b) was synthesized and characterized. It can bind paraquat derivatives more strongly than bis(m-phenylene)-26-crown-8 in solution. It forms pseudorotaxanes with two paraquat derivatives in the solid state. N-Methyl substitution was found to play an important role on the binding strength of lariat ether 3b. Furthermore, due to the introduction of two benzyloxy groups, its binding to paraquat derivatives can be switched off (and back on) by adding K+ (and then dibenzo-18-crown-6), and the disassociation percentage depends on the concentration of the added K+ ions. A novel bis(m-phenylene)-26- crown-8-based lariat ether was synthesized and characterized. It can bind paraquat derivatives more strongly than bis(m-phenylene)-26-crown-8 in solution. It forms pseudorotaxanes with two paraquat derivatives in the solid state. N-Methyl substitution was found to play an important role on the binding strength of the lariat ether. Furthermore, its binding to paraquat derivatives could be switched by adding K+ and dibenzo-18-crown-6.
| Original language | English |
|---|---|
| Pages (from-to) | 5543-5547 |
| Number of pages | 5 |
| Journal | European Journal of Organic Chemistry |
| Issue number | 29 |
| DOIs | |
| State | Published - Oct 2010 |
| Externally published | Yes |
Keywords
- Controlled assembly
- Crown compounds
- Rotaxanes
- Substituent effects
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