A new hydrated crystalline form of <i>N</i>-[(<i>E</i>)-(4-hydroxyphenyl)methylidene]-1<i>H</i>-1,2,4-triazol-3-amine and its antifungal activity
The synthesis, crystal structure, Hirshfeld analysis, and anti-fungal assessment of a new monohydrated Schiff base with a triazole moiety are reported. The structural study revealed the presence of three significant hydrogen bonds (N-H⋯N, O-H⋯N, and O-H⋯O), which contribute to the cohesion of the crystal. These bonds generate two-dimensional layers parallel to the <i>bc</i> plane, built on the basis of rings with the graph-set motifs <i>R</i> <sup>4</sup> <sub>4</sub>(8) and <i>R</i> <sup>4</sup> <sub>4</sub>(24). The crystal structure is further consolidated by π-π inter-actions between similar rings. The anti-fungal activity of the Schiff base was evaluated against three fungi: <i>Fusarium oxysporum</i>, <i>Botrytis cinerea</i>, and <i>Alternaria alternata</i>, showing significant anti-fungal activity, particularly against <i>Alternaria alternata</i>.
Authors
- Aouatef Cherouana (ORCID: https://orcid.org/0000-0002-6301-9628)
- Boualia Boutheina
- Bouhidel Zakaria
- Bendeif El-Eulmi
Institutions
- University Frères Mentouri Constantine 1 (DZ)
- Synchrotron soleil (FR)
- Laboratoire de Cristallographie, Résonance Magnétique et Modélisations (FR)
Publication Details
- Journal
- Acta Crystallographica Section E Crystallographic Communications
- Published
- 2024-12-24
- DOI
- https://doi.org/10.1107/s205698902401209x
- Primary Topic
- Synthesis and biological activity
- Type
- article
- Field-Weighted Citation Impact
- 0.00