The title compound, C 22 H 26 N 2 O 4 , was prepared by reaction of trans-1,2-cyclohexanediamine and 2-hydroxy-3-methoxybenzaldehyde. The molecular structure is stabilized by intramolecular O-HÁ Á ÁN hydrogen bonds.
N,N′-Bis(3-nitrobenzylidene)-trans-1,2-cyclohexanediamine
✍ Scribed by Liu, Zhao-Di ;Tan, Min-Yu ;Zhu, Hai-Liang
- Publisher
- International Union of Crystallography
- Year
- 2005
- Tongue
- English
- Weight
- 325 KB
- Volume
- 61
- Category
- Article
- ISSN
- 1600-5368
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📜 SIMILAR VOLUMES
Single-crystal X-ray study T = 273 K Mean '(C±C) = 0.002 A Ê R factor = 0.048 wR factor = 0.133 Data-to-parameter ratio = 15.0 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.
The title compound, C 17 H 16 Cl 2 N 2 , adopts a 'vault' conformation. The molecules are linked by a pair of C-HÁ Á ÁN hydrogen bonds into a centrosymmetric dimer with an R 2 2 (18) ring. These dimers are linked by a weak centrosymmetricinteraction into a chain along the [001] direction, and these
The title compound, C 20 H 26 N 4 , was prepared by a condensation reaction between p-dimethylaminobenzaldehyde and ethylenediamine. The molecule contains a crystallographically imposed twofold axis of symmetry.