2019年11月1日
Crystal structures of the two isomeric hydrogen-bonded cocrystals 2-chloro-4-nitrobenzoic acid-5-nitroquinoline (1/1) and 5-chloro-2-nitrobenzoic acid-5-nitroquinoline (1/1)
Acta Crystallographica Section E: Crystallographic Communications
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- 巻
- 75
- 号
- 開始ページ
- 1694
- 終了ページ
- 1699
- 記述言語
- 掲載種別
- 研究論文(学術雑誌)
- DOI
- 10.1107/S2056989019013896
The structures of two isomeric compounds of 5-nitroquinoline with chloro-and nitro-substituted benzoic acid, namely, 2-chloro-4-nitrobenzoic acid-5-nitroquinoline (1/1), (I), and 5-chloro-2-nitrobenzoic acid-5-nitroquinoline (1/1), (II), both C7H4ClNO4·C9H6N2O2, have been determined at 190 K. In each compound, the acid and base molecules are held together by an O-H..N hydrogen bond. In the crystal of (I), the hydrogen-bonded acid-base units are linked by a C-H..O hydrogen bond, forming a tape structure along [1 0]. The tapes are stacked into a layer parallel to the ab plane via N-O..π interactions between the nitro group of the base molecule and the quinoline ring system. The layers are further linked by other C-H..O hydrogen bonds, forming a three-dimensional network. In the crystal of (II), the hydrogen-bonded acid-base units are linked into a wide ribbon structure running along [1 0] via C-H..O hydrogen bonds. The ribbons are further linked via another C-H..O hydrogen bond, forming a layer parallel to (110). Weak π-π interactions [centroid-centroid distances of 3.7080 (10) and 3.7543 (9) Å] are observed between the quinoline ring systems of adjacent layers. Hirshfeld surfaces for the 5-nitroquinoline molecules of the two compounds mapped over shape index and d norm were generated to visualize the weak intermolecular interactions.
- リンク情報
- ID情報
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- DOI : 10.1107/S2056989019013896
- eISSN : 2056-9890
- SCOPUS ID : 85074767198