H -Dicyanobiphenyl, C 14 H 8 N 2 , has a normal structure with a twist angle of 31.8 (2) . The molecules stack with overlapping % systems and form chains held together by antiparallel CÐ NÁ Á ÁCÐN interactions. In addition, there are a number of CÐ HÁ Á ÁN interactions.
4,4′-Diiodobiphenyl
✍ Scribed by Britton, Doyle
- Publisher
- International Union of Crystallography
- Year
- 2004
- Tongue
- English
- Weight
- 149 KB
- Volume
- 61
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
H -Diiodobiphenyl, C 12 H 8 I 2 , crystallizes as a homologous isomorph of the high-temperature form of p-diiodobenzene. The molecule is planar and lies on a center of symmetry. Each I atom is in contact with ®ve others at distances between 4.0 and 4.5 A Ê .
📜 SIMILAR VOLUMES
Single-crystal X-ray study T = 193 K Mean '(C±C) = 0.009 A Ê R factor = 0.041 wR factor = 0.101 Data-to-parameter ratio = 25.7 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.
The asymmetric biphenyl title compound, C 14 H 13 ClO 2 , exhibits a significant twist of ca 30 about the central C-C bond.
The title compound, C 12 H 8 I 2 N 2 O, was obtained as an unexpected product while attempting to protect N,N-dibutyl-4-iodoaniline as the N-oxide. It crystallizes as a layer structure. Oxidation of (II) by hydrogen peroxide gives the N-oxide (III). This eliminates butene via a Cope reaction (Adams
The title compound, C 32 H 23 Cl 2 N, was synthesized via the Ullmann reaction. The orientations of the three aromatic rings attached to the vinyl group are determined by the sp 2 state of the vinyl C atoms. The crystal packing is stabilized by weak CÐHÁ Á Á% interactions.