Redox-dependent conformational switching of diphenylacetylenes

Molecules. 2014 Jul 31;19(8):11316-32. doi: 10.3390/molecules190811316.

Abstract

Herein we describe the design and synthesis of a redox-dependent single-molecule switch. Appending a ferrocene unit to a diphenylacetylene scaffold gives a redox-sensitive handle, which undergoes reversible one-electron oxidation, as demonstrated by cyclic voltammetry analysis. (1)H-NMR spectroscopy of the partially oxidized switch and control compounds suggests that oxidation to the ferrocenium cation induces a change in hydrogen bonding interactions that results in a conformational switch.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylene / analogs & derivatives*
  • Acetylene / chemical synthesis
  • Acetylene / chemistry
  • Ions / chemistry
  • Models, Molecular
  • Molecular Conformation*
  • Nuclear Magnetic Resonance, Biomolecular
  • Oxidation-Reduction*

Substances

  • Ions
  • biphenylacetylene
  • Acetylene