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X-ray crystal structure of trans-bis-(pyridin-3-yl)ethyl-ene: comparing the supra-molecular structural features among the symmetrical bis-(n-pyrid-yl)ethyl-enes (n = 2, 3, or 4) constitutional isomers.

Jay QuentinEric W ReinheimerLeonard R MacGillivray
Published in: Acta crystallographica. Section E, Crystallographic communications (2020)
The mol-ecular structure of trans-bis-(pyridin-3-yl)ethyl-ene (3,3'-bpe), C12H10N2, as determined by single-crystal X-ray diffraction is reported. The mol-ecule self-assembles into two dimensional arrays by a combination of C-H⋯N hydrogen bonds and edge-to-face C-H⋯π inter-actions that stack in a herringbone arrangement perpendicular to the crystallographic c-axis. The supra-molecular forces that direct the packing of 3,3'-bpe as well as its packing assembly within the crystal are also compared to those observed within the structures of the other symmetrical isomers trans-1,2-bis-(n-pyrid-yl)ethyl-ene ( n , n '-bpe, where n = n' = 2 or 4).
Keyphrases
  • ionic liquid
  • high resolution
  • electron microscopy
  • dual energy
  • magnetic resonance imaging
  • magnetic resonance
  • solid state
  • contrast enhanced