Crystal and molecular structure of newly synthesized 2,3,2′,3′-Bis{8″,11″-dioxa[4.3.3]propella(3″,4″)}biphenyl
✍ Scribed by Grochowski, Jacek ;Jamrozik, Janusz ;Serda, Paweł ;Zesławski, Wojciech
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 249 KB
- Volume
- 1995
- Category
- Article
- ISSN
- 0947-3440
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✦ Synopsis
Abstract
The title compound 5 was obtained from 2,2′,3,3′‐tetramethylbiphenyl in a multi‐step reaction sequence leading to the bis(propellane). X‐ray structure analysis proved the identity of bis(propellane). In the solid state the molecule possesses roughly a twofold symmetry axis perpendicular to the biphenyl bond. The conformation of the molecule is determined by a 53.5(1)° torsional angle between the biphenyl planes. The propellane bond is parallel to the phenyl plane in both symmetric parts of the molecule, what implies a boat conformation of the fused six‐membered rings.
📜 SIMILAR VOLUMES
The decomposition of Er 2 (SeO 4 ) 3 in the presence of LiF in a sealed gold ampoule at 8701C yielded single crystals of Er 2 (SeO 3 ) 3 . The triclinic crystal structure (P 1 1; Z ¼ 2; a ¼ 698:2ð1Þ; b ¼ 800:6ð1Þ; c ¼ 895:0ð1Þ pm; a ¼ 71:38ð1Þ; b ¼ 70:13ð1Þ; c ¼ 65:87ð1Þ1; R all ¼ 0:0364) contains t
## Abstract The crystal structures of __N__‐aryl‐1,2,3,4‐tetrahydro‐3,3‐dimethyl‐2,4‐quinolinediones bearing methoxy‐ (**1**), methyl‐ (**2**), and chloro‐ (**3**) substituents in 2′‐position of the phenyl ring have been determined by X‐ray crystal structure analysis. The heterocyclic ring in **1–3