Crystal structure and Hirshfeld surface analysis of new polymorph of racemic 2-phenylbutyramide
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RIGIN, Sergei, ARMIJO, Beatrice, KRIVOSHEIN, Arcadius, FONARI, Marina, TIMOFEEVA, Tatiana. Crystal structure and Hirshfeld surface analysis of new polymorph of racemic 2-phenylbutyramide. In: Acta Crystallographica Section E: Crystallographic Communications, 2019, vol. 75, pp. 826-829. ISSN -. DOI: https://doi.org/10.1107/S2056989019007011
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Acta Crystallographica Section E: Crystallographic Communications
Volumul 75 / 2019 / ISSN - /ISSNe 2056-9890

Crystal structure and Hirshfeld surface analysis of new polymorph of racemic 2-phenylbutyramide

DOI:https://doi.org/10.1107/S2056989019007011

Pag. 826-829

Rigin Sergei1, Armijo Beatrice1, Krivoshein Arcadius2, Fonari Marina3, Timofeeva Tatiana4
 
1 New Mexico Highlands University, Department of Chemistry, Las Vegas,
2 University of Houston-Clear Lake,
3 Institute of Applied Physics,
4 Georgia Institute of Technology
 
 
Disponibil în IBN: 16 august 2019


Rezumat

A new polymorph of the title compound, C 10 H13NO, was obtained by recrystallization of the commercial product from a water/ethanol mixture (1:1 v/v). Crystals of the previously reported racemic and homochiral forms of 2-phenylbutyramide were grown from water-acetonitrile solution in 1:1 volume ratio [Khrustalev et al. (2014). Cryst. Growth Des. 14, 3360-3369]. While the previously reported racemic and enantiopure forms of the title compound adopt very similar supramolecular structures (hydrogen-bonded ribbons), the new racemic polymorph is stabilized by a single N - H...O hydrogen bond that links molecules into chains along the c-axis direction with an antiparallel (centrosymmetric) packing in the crystal. Hirshfeld molecular surface analysis was employed to compare the intermolecular interactions in the polymorphs of the title compound.

Cuvinte-cheie
2-phenylbutyramide, crystal structure, Hirshfeld surface analysis, Hydrogen bonds, racemate