In the title compound, C 16 H 15 N 3 OS, molecules form inversionrelated dimers via N-HÁ Á ÁS hydrogen bonds. The structure is further stabilized by intermolecularstacking interactions down the a axis.
Linear and Nonlinear Optical Susceptibilities of 3-Phenylamino-4-phenyl-1,2,4-triazole-5-thione
✍ Scribed by Reshak, A. H.; Stys, D.; Auluck, S.; Kityk, I. V.
- Book ID
- 118268055
- Publisher
- American Chemical Society
- Year
- 2010
- Tongue
- English
- Weight
- 349 KB
- Volume
- 114
- Category
- Article
- ISSN
- 0022-3654
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📜 SIMILAR VOLUMES
The title compound, C 15 H 13 N 3 S, was prepared by the reaction of 1-(2-chloroethyl)benzene with hydrazine and phenyl isothiocyanate. Packing is stabilized by N-HÁ Á ÁS intermolecular hydrogen bonds and C-HÁ Á Á interactions.
Single-crystal X-ray study T = 296 K Mean '(C±C) = 0.003 A Ê R factor = 0.039 wR factor = 0.096 Data-to-parameter ratio = 17.3 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.
In the crystal structure of the title compound, C~16~H~15~N~3~OS, intermolecular N—H...S hydrogen bonds link the molecules together as characteristic dimers, which are further stabilized by weak intermolecular benzene-ring π–π interactions along the __a__-axis direction.