Synthesis and Magnetic Properties of Stable Radical Derivatives Carrying a Phenylacetylene Unit

Molecules. 2018 Feb 9;23(2):371. doi: 10.3390/molecules23020371.

Abstract

A nitronyl nitroxide derivative, 2-phenylethynyl-4,4,5,5-tetramethyl-4,5-dihydro-1H-imidazol-1-oxyl-3-oxide (1), and two verdazyl derivatives carrying a phenylacetylene unit, 1,5-diphenyl-3-phenylethynyl-6-oxo-1,2,4,5-tetrazin-2-yl (2) and 1,5-diisopropyl-3-phenylethynyl-6-oxo-1,2,4,5-tetrazin-2-yl (3), were synthesized and their packing structures were studied by X-ray crystallographic analysis and magnetically characterized in the solid state. While 1 and 3 had an isolated doublet spin state, 2 formed an antiferromagnetically coupled pair (2J/kB = -118 K). Density functional theory (DFT) calculations reveal that the spin density polarized in the phenyl group decreases as the dihedral angle between the phenyl ring and radical plane increases.

Keywords: computational analysis; magnetic property; nitronyl nitroxide; phenylacetylene; stable radical; verdazyl.

MeSH terms

  • Acetylene / analogs & derivatives*
  • Acetylene / chemical synthesis
  • Acetylene / chemistry
  • Computer Simulation
  • Imidazoles / chemical synthesis
  • Imidazoles / chemistry*
  • Magnets / chemistry
  • Molecular Structure
  • Nitrogen Oxides / chemical synthesis
  • Nitrogen Oxides / chemistry*

Substances

  • Imidazoles
  • Nitrogen Oxides
  • phenylacetylene
  • nitroxyl
  • Acetylene