Synthesis, X-ray Structure, Conformational Analysis, and DFT Studies of a Giant <i>s</i>-Triazine <i>bis</i>-Schiff Base
The current work involves the synthesis of 2,2′-(6-(piperidin-1-yl)-1,3,5-triazine-2,4-diyl)<i>bis</i>(hydrazin-2-yl-1-ylidene))<i>bis</i>(methanylylidene))diphenol <b>4</b>, characterization, and the DFT studies of the reported compound. The crystal unit cell par...
Saved in:
| Main Authors: | , , , , , |
|---|---|
| Format: | article |
| Language: | EN |
| Published: |
MDPI AG
2021
|
| Subjects: | |
| Online Access: | https://doaj.org/article/838fde9d0a8c4dcda687255b76aec44d |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| Summary: | The current work involves the synthesis of 2,2′-(6-(piperidin-1-yl)-1,3,5-triazine-2,4-diyl)<i>bis</i>(hydrazin-2-yl-1-ylidene))<i>bis</i>(methanylylidene))diphenol <b>4</b>, characterization, and the DFT studies of the reported compound. The crystal unit cell parameters of <b>4</b> are a = 8.1139(2) Å, b = 11.2637(2) Å, c = 45.7836(8) Å. The unit cell volume is 4184.28(15) Å<sup>3</sup> and Z = 4. It crystallized in the orthorhombic crystal system and <i>Pbca</i> space group. The O…H, N…H, C…H, H…H and C…C intermolecular contacts which affect the crystal stability were quantitatively analyzed using Hirshfeld calculations. Their percentages were calculated to be 9.8, 15.8, 23.7, 46.4, and 1.6% from the whole contacts occurred in the crystal, respectively. Conformational analysis was performed using DFT calculations for 17 suggested conformers and the most stable conformer was found to be the one which is stabilized by two intramolecular O-H…N hydrogen bonding interactions. This conclusion was further revealed by natural bond orbital calculations. |
|---|