Crystal structure and Hirshfeld surface analysis of dimethyl 3-methyl-8-{[4-(trifluoromethyl)phenyl]sulfonyl}-7,8-dihydro-4H-4,6a-epoxybenzo[b]naphtho[1,8-de]azepine-5,6-dicarboxylate
The molecular conformation of the title compound, C29H22F3NO7S, is stable due to the intramolecular C—H...O hydrogen bonds. The central seven-membered ring adopts a distorted chair form. In the 7-oxabicyclo[2.2.1]hepta-2,5-diene unit, the five-membered rings adopt envelope conformations. In the crys...
Saved in:
| Main Authors: | , , , , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
International Union of Crystallography
2025-06-01
|
| Series: | Acta Crystallographica Section E: Crystallographic Communications |
| Subjects: | |
| Online Access: | https://journals.iucr.org/paper?S2056989025004426 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| Summary: | The molecular conformation of the title compound, C29H22F3NO7S, is stable due to the intramolecular C—H...O hydrogen bonds. The central seven-membered ring adopts a distorted chair form. In the 7-oxabicyclo[2.2.1]hepta-2,5-diene unit, the five-membered rings adopt envelope conformations. In the crystal, the molecules are linked by C—H...O and C—H...F interactions, forming sheets parallel to the (002) plane. Additionally, S—O...π and π–π interactions [centroid-to-centroid distance = 3.6159 (7) Å] connect the molecules along the a-axis direction. van der Waals interactions between the molecular sheets reinforce the molecular packing. A Hirshfeld surface analysis was conducted to visualize the various intermolecular interactions, indicating that the largest contribution to the surface contacts is from H...H interactions (37.3%), followed by O...H/H...O (24.1%), F...H/H...F (19.0%), and C...H/H...C (10.3%) interactions. |
|---|---|
| ISSN: | 2056-9890 |