Journal
CHEMICAL COMMUNICATIONS
Volume 55, Issue 16, Pages 2372-2375Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c9cc00599d
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Funding
- National Natural Science Foundation of China [21771145, 21472149, 21402151]
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Two new tetracationic cyclophanes 1 and 2 containing tetra-phenylethene and bipyridinium moieties were synthesized via a two-step S(N)2 reaction. These water-soluble cyclophanes with a cationic and hydrophobic cavity exhibited selective recognition for amino acids (e.g. tryptophan) and adenosine derivatives (e.g. ATP) via electrostatic and pi-pi interactions in water.
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