Benzene-1,2,4,5-tetracarboxylic acid dimethyl sulfoxide disolvate: a redetermination at 150 K
✍ Scribed by Dale, Sophie H. ;Elsegood, Mark R. J.
- Publisher
- International Union of Crystallography
- Year
- 2003
- Tongue
- English
- Weight
- 165 KB
- Volume
- 59
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
The title compound, C 10 H 6 O 8 .2C 2 H 6 OS, one of the few known examples of the cocrystallization of pyromellitic acid with common organic solvents, has been previously analysed by single-crystal X-ray diffraction at 296 K [Jin, Pan, Shen, Li & Hu (2003). Acta Cryst. C59, o205±o206]. We present here a redetermination at low temperature (150 K). The centrosymmetric compound crystallizes in space group P1 and exhibits co-operative strong (acid)OÐHÁ Á ÁO(solvent) and weaker (solvent)CÐHÁ Á ÁO(acid) hydrogen-bonding interactions, giving rise to a one-dimensional ribbon structure along the bc diagonal of the unit cell.
📜 SIMILAR VOLUMES
In the title compound, C 10 H 16 O 5 , the carboxylate group at the C-2 position is axial, but that at C-5 is equatorial. These carboxylate groups form hydrogen-bonded rings [average OÁ Á ÁO H distance = 2.64 (1) A Ê ] across the inversion centers at ( 1 2 , 0, 0) and ( 1 2 , 1 2 , 1 2 ), respective
In the title compound, C 20 H 14 N 2 O 8 Á2C 3 H 7 NO, the essentially planar C 20 H 14 N 2 O 8 molecule is centrosymmetric and is hydrogen bonded via the carboxylic acid H atoms to the aldehyde O atom of the dimethylformamide molecules.