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>.

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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
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article

A new hydrated crystalline form of N-[(E)-(4-hydroxyphenyl)methylidene]-1H-1,2,4-triazol-3-amine and its antifungal activity

Aouatef Cherouana, Boualia Boutheina, Bouhidel Zakaria, Bendeif El-Eulmi
Acta Crystallographica Section E Crystallographic Communications
Synthesis and biological activity
article

A new hydrated crystalline form of N-[(E)-(4-hydroxyphenyl)methylidene]-1H-1,2,4-triazol-3-amine and its antifungal activity

Aouatef Cherouana, Boualia Boutheina, Bouhidel Zakaria, Bendeif El-Eulmi
article en

Abstract

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>.

Acta Crystallographica Section E Crystallographic CommunicationsVol. 81(1)
University Frères Mentouri Constantine 1 (DZ), Synchrotron soleil (FR), Laboratoire de Cristallographie, Résonance Magnétique et Modélisations (FR)
Clean water and sanitation
Openalex Percentile: Top 82%
Synthesis and biological activity
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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 — Aouatef Cherouana, Boualia Boutheina, et al. · Acta Crystallographica Section E Crystallographic Communications (2024) | TGRS Research Map | TGRS