Abstract

In the title compound, C24H18N4O4, the plane of the phenyl ring is inclined to those of the toluene ring and the di­nitro-substituted benzene ring by 66.96 (19) and 47.06 (18)°, respectively, while the planes of the two benzene rings are inclined to one another by 36.26 (19)°. There is an intra­molecular N—H⋯O hydrogen bond between the NH group and the O atom of a nitro group, forming an S(6) ring motif. In the crystal, mol­ecules are linked by C—H⋯O hydrogen bonds and C—H⋯π inter­actions, forming a three-dimensional network. There are also weak π–π inter­actions present involving the phenyl ring and the di­nitro-substituted benzene ring [inter-centroid distance = 3.741 (2) Å].

Highlights

  • In the title compound, C24H18N4O4, the plane of the phenyl ring is inclined to those of the toluene ring and the dinitrosubstituted benzene ring by 66.96 (19) and 47.06 (18), respectively, while the planes of the two benzene rings are inclined to one another by 36.26 (19)

  • H atoms treated by a mixture of independent and constrained refinement max = 0.53 e Å3

  • In contrast with the parent pent-2-en-4-yn-1-one compound (Vologzhanina et al, 2014) the benzene rings at C1 and C5 atoms are twisted with respect to one another, with a dihedral angle of

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Summary

Introduction

C24H18N4O4, the plane of the phenyl ring is inclined to those of the toluene ring and the dinitrosubstituted benzene ring by 66.96 (19) and 47.06 (18) , respectively, while the planes of the two benzene rings are inclined to one another by 36.26 (19). There is an intramolecular N—H O hydrogen bond between the NH group and the O atom of a nitro group, forming an S(6) ring motif. Molecules are linked by C—H O hydrogen bonds and C—H interactions, forming a three-dimensional network. Absorption correction: multi-scan (SADABS; Bruker, 2005)

Results
Conclusion

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