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 |
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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 |
Scopus Subject Areas
- Organic Chemistry
User-Defined Keywords
- cation π interactions
- host-guest chemistry
- macrocycle
- nonplanar hydrocarbon
- tetraphenylene