The title compound, C 16 H 12 BrClN 4 O, contains two benzene rings and a triazole ring which is substituted at the 1,2,4positions. The crystal structure of (I) is stabilized by NÐ HÁ Á ÁO and %±% stacking interactions.
4-[(4-Chlorobenzylidene)amino]-3-(3-hydroxypropyl)-1,2,4-triazole-5(4H)-thione
✍ Scribed by Zou, Kai-Huang ;Zhang, Li-Xue ;Jin, Jian-Yu ;Xiao, Hong-Ping ;Zhang, Kang
- Book ID
- 111752055
- Publisher
- International Union of Crystallography
- Year
- 2006
- Tongue
- English
- Weight
- 122 KB
- Volume
- 62
- Category
- Article
- ISSN
- 1600-5368
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In the title compound, C 8 H 8 N 4 OS, the planar triazole ring is effectively coplanar with the benzene ring, which facilitates the formation of three intramolecular interactions N-HÁ Á ÁS (leading to a thione tautomer in the solid state), O-HÁ Á ÁN and C-HÁ Á ÁN. Intermolecular N-HÁ Á ÁS interacti
In the title molecule, C 15 H 12 ClN 3 S, the dihedral angles made by the substituted phenyl and benzyl rings with the triazole ring are 81.39 (10) and 63.59 (10) , respectively. The crystal structure is stabilized by NÐHÁ Á ÁS, CÐHÁ Á ÁCl and CÐHÁ Á Á% interactions.
In the title compound, C 12 H 11 N 7 OS, the dihedral angles made by the thione-substituted triazole ring with the other triazole ring and the benzene ring are 71.56 (2) and 47.89 (3) , respectively. Inter-and intramolcular hydrogen-bond interactions stabilize the structure.
In the molecule of the title compound, C 5 H 7 N 7 S, the essentially planar triazole ring and the 4-amino-5-mercapto-1,2,4-triazole moiety make a dihedral angle of 70.97 (5) . In the crystal structure, weak intermolecular N-HÁ Á ÁN and N-HÁ Á ÁS hydrogen bonds stabilize the packing.