(E)-Acetophenone O-(3,4,5,6-Tetrafluoro-2-pyridyl)oxime, Formed by 2-Substitution of Pentafluoropyridine by (E)-Acetophenone Oximate
Publication Type
Original research
Authors
  • Jondi, W.J
  • Banks, R.E
  • Pritchard, R.G
  • Tipping, A.E

Despite the oxyimino chain being unconjugated [N-O 1.434 (2) and C-N 1.278 (2) angstrom] in the title compound, C13H8F4N2O, the planar alpha-phenylethylimino and tetrafluoro-2-oxopyridine moieties are only slightly twisted relative to each other [C-O-N-C 167.6 (2)-degrees]. This facilitates stacking along the ac diagonal so that fluorinated pyridine substituents alternate with non-fluorinated phenyl rings.

Journal
Title
Acta Crystallographica Section C: Crystal Structure Communications , Volume 51 (2): 293- 295
Publisher
--
Publisher Country
Palestine
Publication Type
Both (Printed and Online)
Volume
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Year
1995
Pages
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