2-(1-Naphthyliminomethyl)phenol
✍ Scribed by Cheng, Kui ;Zhu, Hai-Liang ;Liu, Jing-Jing ;Gao, Meng ;Zeng, Jun-He
- Book ID
- 111752046
- Publisher
- International Union of Crystallography
- Year
- 2006
- Tongue
- English
- Weight
- 305 KB
- Volume
- 62
- Category
- Article
- ISSN
- 1600-5368
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📜 SIMILAR VOLUMES
The title compound, C 12 H 17 N 3 O, was obtained by the direct solvent-free reaction of salicylaldehyde with 1-amino-4methylpiperazine. The piperazine ring adopts a chair conformation. In the crystal structure, strong intramolecular O-HÁ Á ÁN hydrogen bonds, weak intermolecular C-HÁ Á ÁO hydrogen b
The title compound, C 13 H 18 N 2 O 2 , exists in the enol-imine tautomeric form with a strong intramolecular O-HÁ Á ÁN hydrogen bond [OÁ Á ÁN = 2.5795 (18) A ˚], and the morpholine ring adopts an almost perfect chair conformation.
In the title compound, C 9 H 7 N 3 OS, the structure is stabilized by intramolecular O-HÁ Á ÁN and intermolecular C-HÁ Á ÁO and C-HÁ Á ÁN hydrogen bonds. The intermolecular hydrogen bonds link the molecules into a three-dimensional supramolecular network.