| Literature DB >> 27862733 |
Daniel Beaudoin1, Frank Rominger1, Michael Mastalerz1.
Abstract
The strategy of chirality-assisted synthesis, which makes use of enantiomerically pure building blocks that are designed to associate in a single geometric orientation, was applied to synthesize an octameric hydrogen-bonded capsule with a cavity volume of 2300 Å3 . This cube-shaped capsule forms even host-guest complexes with tetraalkylammonium ions, and accommodates the large tetrahexadecylammonium cation in its cavity. The use of an enantiopure building block was shown to be highly beneficial for capsule formation, whereas its racemate also generates a large amount of ill-defined aggregates in solution and crystallizes as a hydrogen-bonded network.Entities:
Keywords: NMR spectroscopy; chirality-assisted synthesis; encapsulation; host-guest chemistry; tribenzotriquinacenes
Year: 2016 PMID: 27862733 DOI: 10.1002/anie.201609073
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336