| Literature DB >> 33498575 |
Jing Li1,2, Ying Han1, Chuan-Feng Chen1,2.
Abstract
Starting from the enantiopure precursors, a pair of chiral macrocyclic arenes named helic[1]triptycene[3]arenes were conveniently synthesized. The circular dichroism (CD) spectra of the enantiomeric macrocyclic arenes exhibited mirror images, and the X-ray single crystal structures confirmed their absolute conformations as well. Moreover, the macrocyclic arenes showed strong complexation with secondary ammonium and primary ammonium salts containing aminoindan groups. In particular, the chiral macrocyclic arenes exhibited enantioselective recognition ability towards the chiral secondary ammonium salts containing aminoindan groups with an enantioselective ratio up to 3.89.Entities:
Keywords: ammonium salts; enantioselective recognition; helic[1]triptycene[3]arene; macrocyclic arene
Year: 2021 PMID: 33498575 PMCID: PMC7864338 DOI: 10.3390/molecules26030536
Source DB: PubMed Journal: Molecules ISSN: 1420-3049 Impact factor: 4.411