Tandem Reactivity of a Self-Assembled Cage Catalyst with Endohedral Acid Groups

J Am Chem Soc. 2018 Jul 5;140(26):8078-8081. doi: 10.1021/jacs.8b03984. Epub 2018 Jun 20.

Abstract

Self-assembly of a carboxylic acid-containing ligand into an Fe4L6 iminopyridine cage allows endohedral positioning of the acid groups while maintaining a robust cage structure. The cage is an effective supramolecular catalyst, providing up to 1000-fold rate enhancement of acetal solvolysis. This enhanced reactivity allows a tandem deprotection/cage-to-cage interconversion that cannot be achieved with other acid catalysts. The combination of rate enhancements and sequestration of the reactive function confers both activity and selectivity on the process, mimicking enzymatic behavior.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Carboxylic Acids / chemistry*
  • Catalysis
  • Coordination Complexes / chemical synthesis*
  • Coordination Complexes / chemistry
  • Ligands
  • Models, Molecular
  • Molecular Structure
  • Pyridines / chemistry*

Substances

  • Carboxylic Acids
  • Coordination Complexes
  • Ligands
  • Pyridines