A simple and visual approach for enantioselective recognition through supramolecular gels with specific selectivity.
Chem Commun (Camb)
; 55(66): 9873-9876, 2019 Aug 13.
Article
in En
| MEDLINE
| ID: mdl-31364621
ABSTRACT
Simple (S)- or (R)-1,1'-binaphthalene-2,2'-diol-3-carbaldehyde was found to enantioselectively self-assemble to form a gel or solution with one enantiomer of chiral amines, 1,1'-binaphthalene-2,2'-diamine, through intermolecular hydrogen bond, HH, π-π stacking, and chirality-induced interactions. The enantioselective recognition is visual and highly selective with little interference from similar organic compounds and common cations and anions.
Full text:
1
Database:
MEDLINE
Language:
En
Journal:
Chem Commun (Camb)
Journal subject:
QUIMICA
Year:
2019
Type:
Article