Synthesis, crystal structure and Hirshfeld surface analysis of 2-(perfluorophenyl)acetamide in comparison with some related compounds

The mol­ecular and crystal structures of the title compound, C8H4F5NO, were examined by single-crystal X-ray diffraction and Hirshfeld surface analysis. The title compound was synthesized by a new method at the interface of aqueous solutions of LiOH and penta­fluoro­phenyl­aceto­nitrile. In the crystal, hydrogen bonds and π-halogen inter­actions connect the mol­ecules into double layers. Analysis of the Hirshfeld surface showed that the most important contributions to the crystal packing are made by F⋯F (30.4%), C⋯F/F⋯C (22.9%), O⋯H/H⋯O (14.9%), H⋯F/F⋯H (14.0%) and H⋯H (10.2%) contacts. The Hirshfeld surfaces of analogues of the title compound were compared and the effect of perfluorination on the crystal packing was shown. © 2022

Authors
Novikov A.P. 1, 2 , Bezdomnikov A.A.2 , Grigoriev M.S.2 , German K.E.2
Publisher
International Union of Crystallography
Language
English
Pages
80-83
Status
Published
Volume
78
Year
2022
Organizations
  • 1 Peoples' Friendship University of Russia (RUDN University), 6 Miklukho-Maklaya St, Moscow, 117198, Russian Federation
  • 2 Frumkin Institute of Physical Chemistry and Electrochemistry Russian, Academy of Sciences, 1 Leninsky Prospekt bldg 4, Moscow, 119071, Russian Federation
Keywords
Acetamide; Crystal structure; Hirshfeld surface analysis; Hydrogen bonds; Perfluorophenyl
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