The title compound, C 16 H 14 Br 2 N 2 O 4 , has been synthesized by the reaction of 1,2-bis(aminooxy)ethane with 5-bromo-2hydroxybenzaldehyde in ethanol. The molecule is centrosymmetric. Intramolecular O-HÁ Á ÁN hydrogen bonding is observed between hydroxy groups and oxime N atoms.
5,5′-Bis(diethylamino)-2,2′-[ethylenedioxybis(nitrilomethylidyne)]diphenol
✍ Scribed by Zhang, Yan-Ping ;Chen, Xiao ;Shi, Jun-Yan ;Xu, Li ;Dong, Wen-Kui
- Publisher
- International Union of Crystallography
- Year
- 2007
- Tongue
- English
- Weight
- 525 KB
- Volume
- 63
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
The centrosymmetric title compound, C 24 H 34 N 4 O 4 , has been characterized structurally by 1 H NMR and X-ray crystallography. The two benzene rings are parallel to each other. The compound forms intramolecular hydrogen bonds, where the oxime group acts as a hydrogen-bond donor and the OH group acts as a hydrogen-bond acceptor.
📜 SIMILAR VOLUMES
In the title molecule, C 17 H 18 Cl 2 N 2 O, the angle between the mean planes of the 2,5-dichlorophenylimino and phenol groups is 19.5 (5) . The two ethyl groups adopt a synclinal conformation. The crystal structure is stabilized by intermolecularstacking interactions between adjacent 2,5dichloroph
The 2,4-bis(dialkylamino)-1,5-dimethyl-1,5,2,4-diazadiphosphorinan-6-ones la and lb (R = CH3, a; C2H5, b) are thermally unstable. and are transformed into the bicyclic species 2 when heated to 150°C (2 Torr). The reactions of la and lb with elemental sulfur lead to the P,P'-disulfides 4a and 4b as a