Abstract
A highly unsymmetrical trisubstituted tetraphenylene was designed and synthesized as a novel superamolecular scaffold for an unexpected trans-meso tetraphenylene macrocycle, whose structure was unequivocally characterized by an X-ray crystallographic analysis. With the defined and electron-rich aromatic cavity, this macrocycle could be further modified to be a potential host for organic cations with biological interest.
| Original language | English |
|---|---|
| Article number | st-2016-w0311-c |
| Pages (from-to) | 2095-2100 |
| Number of pages | 6 |
| Journal | Synlett |
| Volume | 27 |
| Issue number | 14 |
| DOIs | |
| Publication status | Published - 1 Sept 2016 |
User-Defined Keywords
- cation π interactions
- host-guest chemistry
- macrocycle
- nonplanar hydrocarbon
- tetraphenylene