Arylazopyrazoles: azoheteroarene photoswitches offering quantitative isomerization and long thermal half-lives

J Am Chem Soc. 2014 Aug 27;136(34):11878-81. doi: 10.1021/ja505444d. Epub 2014 Aug 14.

Abstract

Arylazopyrazoles, a novel class of five-membered azo photoswitches, offer quantitative photoswitching and high thermal stability of the Z isomer (half-lives of 10 and ∼1000 days). The conformation of the Z isomers of these compounds, and also the arylazopyrroles, is highly dependent on the substitution pattern on the heteroarene, allowing a twisted or planar geometry, which in turn has a significant impact on the electronic spectral properties of the compounds.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Azo Compounds / chemistry*
  • Hydrocarbons, Aromatic / chemistry*
  • Isomerism
  • Molecular Structure
  • Photochemical Processes
  • Pyrazoles / chemistry*
  • Spectrophotometry, Ultraviolet
  • Temperature
  • Time Factors

Substances

  • Azo Compounds
  • Hydrocarbons, Aromatic
  • Pyrazoles