The crystal structure of the title compound, C 23 H 22 O 2 , which exists in the enol form, is stabilized by an intramolecular hydrogen bond. The dihedral angle between the naphthyl ring system and the aromatic ring of the t-BuC 6 H 4 group is 23.50 (10) .
3-(Biphenyl-1-yl)-1-(4-tert-butylphenyl)-3-hydroxyprop-2-en-1-one
✍ Scribed by Zheng, Chun-Yang ;Zheng, Jing ;Wang, Dun-Jia
- Publisher
- International Union of Crystallography
- Year
- 2007
- Tongue
- English
- Weight
- 504 KB
- Volume
- 63
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
In the title compound, C 25 H 24 O 2 , the molecular structure exists in a cis-enol form which is stabilized by an intramolecular O-HÁ Á ÁO hydrogen bond. This hydrogen bond is described as an approximately symmetrical hydrogen bond. The three methyl groups are disordered over two positions, with a site occupancy ratio of ca 4:1.
📜 SIMILAR VOLUMES
The title compound, C~21~H~16~O, was prepared from biphenyl-4-carbaldehyde and acetophenone. The molecule is essentially planar.
The title compound, C 21 H 15 FO, crystallizes with two molecules in the asymmetric unit, which differ only in the signs of their torsion angles. Nevertheless, the two molecules are not related by any crystallographic symmetry element. The dihedral angles between the two phenyl rings of the biphenyl
The title compound, C~22~H~18~O~2~, was prepared from biphenyl-4-carbaldehyde and 4-methoxyacetophenone. The molecule deviates significantly from planarity.
The title compound, C~21~H~15~ClO, was prepared from biphenyl-4-carbaldehyde and 4-chloroacetophenone. Single crystals were obtained from acetone. The compound is isostructural with the corresponding Br compound. The molecule deviates significantly from planarity.
The title compound, C~21~H~15~BrO, was obtained from 4-bromoacetophenone and biphenyl-4-carbaldehyde. The geometry of the molecule is unexceptional. The compound crystallizes isostructurally with the corresponding chloro compound.