Different behavior of nitrenes and carbenes on photolysis and thermolysis: formation of azirine, ylidic cumulene, and cyclic ketenimine and the rearrangement of 6-phenanthridylcarbene to 9-phenanthrylnitrene

J Org Chem. 2005 Sep 30;70(20):7947-55. doi: 10.1021/jo050898g.

Abstract

Flash vacuum thermolysis (FVT) of 9-azidophenanthrene 8, 6-(5-tetrazolyl)phenanthridine 18, and [1,2,3]triazolo[1,5-f]phenanthridine 19 yields 9-cyanofluorene 12 as the principal product and 4-cyanofluorene as a minor product. In all cases, when the product is condensed at or below 77 K, the seven-membered ring ketenimine 24 is detectable by IR spectroscopy (1932 cm(-1)) up to 200 K. Photolysis of Ar matrix isolated 8 at lambda = 308 or 313 nm generates at first the azirine 26, rapidly followed by the ylidic cumulene 27. The latter reverts to azirine 26 at lambda > 405 nm, and the azirine reverts to the ylidic cumulene at 313 nm. Nitrene 9 is observed by ESR spectroscopy following FVT of either azide 8, tetrazole 18, or triazole 19 with Ar matrix isolation of the products. Nitrene 9 and carbene 21 are observed by ESR spectroscopy in the Ar matrix photolyses of azide 8 and triazole 19, respectively.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Azirines / chemical synthesis*
  • Electron Spin Resonance Spectroscopy
  • Ethylenes / chemical synthesis*
  • Hot Temperature
  • Hydrocarbons / chemistry
  • Imines / chemical synthesis
  • Imines / chemistry*
  • Ketones / chemical synthesis*
  • Methane / analogs & derivatives*
  • Methane / chemistry
  • Models, Molecular
  • Phenanthridines / chemical synthesis
  • Phenanthridines / chemistry*
  • Photolysis*
  • Spectrophotometry
  • Thermodynamics

Substances

  • Azirines
  • Ethylenes
  • Hydrocarbons
  • Imines
  • Ketones
  • Phenanthridines
  • carbene
  • phenylnitrene
  • ketene
  • Methane