4.8 Article

Template Synthesis of Three-Dimensional Hexakisimidazolium Cages

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 57, Issue 18, Pages 5161-5165

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201713240

Keywords

cage compounds; carbenes; photochemical cycloaddition; supramolecular chemistry; template synthesis

Funding

  1. NSFC [21722105, 21371036]
  2. FM and EM International Joint Laboratory of Northwest University Xi'an
  3. DFG [SFB 858, IRTG 2027]

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A procedure for the synthesis of three-dimensional hexakisimidazolium cage compounds has been developed. The reaction of the trigonal trisimidazolium salts H3L(PF6)(3), decorated with three N-olefinic pendants, and silver oxide yielded trinuclear trisilver(I) hexacarbene molecular cylinders of the type [Ag3L2](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.

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