The title compound, [Fe(C 5 H 5 )(C 19 H 15 ClN)], a new ketiminecontaining ferrocenyl derivative, has been synthesized and characterized structurally. Conjugation between the two benzene rings and the imine group is not observed. In addition, there are no significant intermolecular interactions.
2-{(1E)-1-[(4-Chlorophenyl)imino]ethyl}-4-methylphenol
✍ Scribed by Chang, Jian-Guo
- Book ID
- 104491908
- Publisher
- International Union of Crystallography
- Year
- 2007
- Tongue
- English
- Weight
- 523 KB
- Volume
- 63
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
The title compound, C~15~H~14~ClNO, displays a trans configuration with respect to the C=N double bond [C—C=N—C = 175.3 (2)°], with a twist by 58.67 (8)° of the two benzene rings about the cental C=N bond. The crystal structure is stabilized by intramolecular O—H...N and intermolecular C—H...O hydrogen bonds.
📜 SIMILAR VOLUMES
The title compound, C~23~H~19~ClN~2~O~2~, has been obtained by the reaction of (__Z__)-4-(4-chlorobenzylidene)-2-phenyloxazol-5(4__H__)-one and benzylamide. The molecules are connected by two N—H...O intermolecular hydrogen bonds to form helicoidal chains running parallel to the __c__ axis.
The crystal structure of the title compound, C 16 H 17 NO 2 , contains two independent molecules in the asymmetric unit. Both molecules adopt the phenol-imine tautomeric form, with strong intramolecular O-HÁ Á ÁN hydrogen bonds. The crystal packing is stabilized by van der Waals interactions.
The title compound, C 12 H 10 ClNO 2 , was synthesized by the reaction of ethyl cyanocaetate with 4-chlorobenzaldehyde in ethanol under microwave irradiation. In the crystal structure, weak intermolecular C-HÁ Á ÁO hydrogen bonds link the molecules into centrosymmetric dimers, which are held togethe
The title compound, C~17~H~12~Cl~2~O, crystallizes in a centrosymmetric space group. The dihedral angle between the two benzene rings is 24.7 (1)°. The crystal packing is characterized by non-classical C—H...O and C—H...Cl inter- and intramolecular hydrogen bonds.