Abstract

In the title compound, C7H6F3NO2, all the non-H atoms except for one of the F atoms lie on a crystallographic mirror plane. In the crystal, the mol­ecules are linked into inversion dimers by pairs of C—H⋯F inter­actions, forming R 2 2(10) loops. These dimers are connected into C(6) chains along [001] through N—H⋯O hydrogen bonds. Aromatic π–π stacking inter­actions [centroid-centroid separation = 3.8416 (10) A°] connect the mol­ecules into a three-dimensional network.

Highlights

  • In the title compound, C7H6F3NO2, all the non-H atoms except for one of the F atoms lie on a crystallographic mirror plane

  • H atoms treated by a mixture of independent and constrained refinement max = 0.37 e Å3

  • The molecules are linked into inversion dimers by pairs of C—H F interactions, forming R22(10)

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Summary

Bruker APEXII CCD diffractometer

Refinement a Department of Studies and Research in Chemistry, U.C.S., Tumkur University, Tumkur, Karnataka 572 103, India, bDepartment of Studies and Research in Chemistry, Tumkur University, Tumkur, Karnataka 572 103, India, cDepartment of Studies and Research in Physics, U.C.S., Tumkur University, Tumkur, Karnataka. 572 103, India, and dDepartment of Studies in Physics, University of Mysore, Manasagangotri, Mysore, India. H atoms treated by a mixture of independent and constrained refinement max = 0.37 e Å3. R factor = 0.065; wR factor = 0.180; data-to-parameter ratio = 8.7. The molecules are linked into inversion dimers by pairs of C—H F interactions, forming R22(10). Aromatic – stacking interactions [centroid-centroid separation = 3.8416 (10) A ]. Connect the molecules into a three-dimensional network. University of Mysore, Mysore, for collecting the data

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