Quantifying the working stroke of tetrathiafulvalene-based electrochemically-driven linear motor-molecules

Chem Commun (Camb). 2006 Jan 14:(2):144-6. doi: 10.1039/b511575b. Epub 2005 Oct 10.

Abstract

A highly constrained [2]rotaxane, constructed in such a way that the tetracationic cyclobis(paraquat-p-phenylene) ring is restricted to reside on a monopyrrolotetrathiafulvalene unit, has been synthesised and characterised. This design allows the deslipping free energy barrier for the tetracationic ring in all three redox states of the rotaxane to be determined.

MeSH terms

  • Electrochemistry
  • Heterocyclic Compounds / chemistry*
  • Kinetics
  • Molecular Structure
  • Oxidation-Reduction
  • Rotaxanes / chemical synthesis*
  • Rotaxanes / chemistry
  • Spectrophotometry

Substances

  • Heterocyclic Compounds
  • Rotaxanes
  • tetrathiafulvalene