| Literature DB >> 29394472 |
Li-Ying Sun1, Narayan Sinha2, Tao Yan1, Yi-Shou Wang1, Tristan T Y Tan2, Le Yu1, Ying-Feng Han1, F Ekkehardt Hahn2.
Abstract
A procedure for the synthesis of three-dimensional hexakisimidazolium cage compounds has been developed. The reaction of the trigonal trisimidazolium salts H3 L(PF6 )3 , decorated with three N-olefinic pendants, and silver oxide yielded trinuclear trisilver(I) hexacarbene molecular cylinders of the type [Ag3 L2 ]3+ with the olefinic pendants from the two different tricarbene ligands arranged in three pairs. Subsequent UV irradiation gave three cyclobutane links between the two tris-NHC ligands in three [2+2] cycloaddition reactions, thereby generating a three-dimensional hexakis-NHC ligand. Removal of the metal ions resulted in the formation of three-dimensional hexakisimidazolium cages with a large internal cavity.Entities:
Keywords: cage compounds; carbenes; photochemical cycloaddition; supramolecular chemistry; template synthesis
Year: 2018 PMID: 29394472 DOI: 10.1002/anie.201713240
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336