A strategy utilizing a recyclable macrocycle transporter for the efficient synthesis of a triazolium-based [2]rotaxane

Angew Chem Int Ed Engl. 2014 Jul 1;53(27):6914-9. doi: 10.1002/anie.201403765. Epub 2014 Jun 6.

Abstract

A general synthesis of triazolium-containing [2]rotaxanes, which could not be accessed by other methods, is reported. It is based on a sequential strategy starting from a well-designed macrocycle transporter which contains a template for dibenzo-24-crown-8 and a N-hydroxysuccinimide (NHS) moiety. The sequence is: 1) synthesis by slippage of a [2]rotaxane building-block; 2) its elongation at its NHS end; 3) the delivery of the macrocycle to the elongated part of the axle by an induced translational motion; 4) the contraction process to yield the targeted [2]rotaxane and recycle the initial transporter.

Keywords: macrocycles; rotaxanes; structure elucidation; supramolecular chemistry; template synthesis.

MeSH terms

  • Ammonium Compounds / chemistry
  • Crown Ethers / chemistry
  • Macrocyclic Compounds / chemistry
  • Rotaxanes / chemical synthesis
  • Rotaxanes / chemistry*
  • Succinimides / chemistry
  • Triazoles* / chemistry

Substances

  • Ammonium Compounds
  • Crown Ethers
  • Macrocyclic Compounds
  • Rotaxanes
  • Succinimides
  • Triazoles
  • dibenzo-24-crown-8
  • N-hydroxysuccinimide