N′-(4-Hydroxybenzylidene)isonicotinohydrazide
✍ Scribed by Deng, Qi-Liang ;Yu, Ming ;Chen, Xin ;Diao, Chun-Hua ;Jing, Zuo-Liang ;Fan, Zhi
- Publisher
- International Union of Crystallography
- Year
- 2005
- Tongue
- English
- Weight
- 329 KB
- Volume
- 61
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
The title compound, C 13 H 11 N 3 O 2 , was prepared by the reaction of pyridine-4-carboxylic acid hydrazide and phydroxybenzaldehyde in ethanol. In the crystal structure, all non-H atoms are coplanar, with an r.m.s. deviation of 0.096 A ˚. N-HÁ Á ÁN, O-HÁ Á ÁN and O-HÁ Á ÁO intermolecular hydrogen bonds stabilize the structure.
📜 SIMILAR VOLUMES
The bond lengths in the title compound, C 13 H 11 N 3 O 2 ÁH 2 O indicate that the organic molecule exists in the keto form. A network of O-HÁ Á ÁO, O-HÁ Á ÁN and N-HÁ Á ÁO hydrogen bonds helps to consolidate the crystal packing.
In the title compound, C 20 H 16 ClN 3 O 2 , the central benzene ring makes dihedral angles of 68.91 (5) and 60.23 (5) with the chlorobenzene ring and the pyridine ring, respectively. The packing is stabilized by intermolecular N-HÁ Á ÁO hydrogen bonds and weak, non-classical intermolecular C-HÁ Á Á