AI Article Synopsis

  • The compound CHFNS is synthesized from 2-(tri-fluoro-methyl)aniline through a multi-step reaction and features a non-centrosymmetric structure with one asymmetric unit.
  • The molecule consists of two aromatic rings that are twisted significantly due to steric hindrance from the tri-fluoro-methyl group.
  • The crystal arrangement is stabilized by weak C-H⋯N and C-H⋯F hydrogen bonds, along with π-π stacking interactions, and further analysis was conducted using Hirshfeld surface analysis and interaction energy calculations.

Article Abstract

The title compound, CHFNS, was synthesized from 2-(tri-fluoro-meth-yl)aniline by a multi-step reaction. It crystallizes in the non-centrosymmetric space group 2, with one mol-ecule in the asymmetric unit, and is constructed from a pair of aromatic rings [2-(tri-fluoro-meth-yl)phenyl and tetra-zole], which are twisted by 76.8 (1)° relative to each other because of significant steric hindrance of the tri-fluoro-methyl group at the position of the benzene ring. In the crystal, very weak C-H⋯N and C-H⋯F hydrogen bonds and aromatic π-π stacking inter-actions link the mol-ecules into a three-dimensional network. To further analyse the inter-molecular inter-actions, a Hirshfeld surface analysis, as well as inter-action energy calculations, were performed.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6727050PMC
http://dx.doi.org/10.1107/S2056989019011459DOI Listing

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