{"title":"N-[(E)-(4-羟基苯基)甲基二烯]- 1h -1,2,4-三唑-3胺的水合结晶及其抗真菌活性","authors":"Boualia Boutheina, Bouhidel Zakaria, Aouatef Cherouana, Bendeif El-Eulmi","doi":"10.1107/S205698902401209X","DOIUrl":null,"url":null,"abstract":"<p><p>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>.</p>","PeriodicalId":7367,"journal":{"name":"Acta Crystallographica Section E: Crystallographic Communications","volume":"81 Pt 1","pages":"80-84"},"PeriodicalIF":0.5000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11701766/pdf/","citationCount":"0","resultStr":"{\"title\":\"A new hydrated crystalline form of <i>N</i>-[(<i>E</i>)-(4-hy-droxy-phen-yl)methyl-idene]-1<i>H</i>-1,2,4-triazol-3-amine and its anti-fungal activity.\",\"authors\":\"Boualia Boutheina, Bouhidel Zakaria, Aouatef Cherouana, Bendeif El-Eulmi\",\"doi\":\"10.1107/S205698902401209X\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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>.</p>\",\"PeriodicalId\":7367,\"journal\":{\"name\":\"Acta Crystallographica Section E: Crystallographic Communications\",\"volume\":\"81 Pt 1\",\"pages\":\"80-84\"},\"PeriodicalIF\":0.5000,\"publicationDate\":\"2025-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11701766/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Acta Crystallographica Section E: Crystallographic Communications\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1107/S205698902401209X\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CRYSTALLOGRAPHY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta Crystallographica Section E: Crystallographic Communications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1107/S205698902401209X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CRYSTALLOGRAPHY","Score":null,"Total":0}
A new hydrated crystalline form of N-[(E)-(4-hy-droxy-phen-yl)methyl-idene]-1H-1,2,4-triazol-3-amine and its anti-fungal 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 bc plane, built on the basis of rings with the graph-set motifs R44(8) and R44(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: Fusarium oxysporum, Botrytis cinerea, and Alternaria alternata, showing significant anti-fungal activity, particularly against Alternaria alternata.
期刊介绍:
Acta Crystallographica Section E: Crystallographic Communications is the IUCr''s open-access structural communications journal. It provides a fast, simple and easily accessible publication mechanism for crystal structure determinations of inorganic, metal-organic and organic compounds. The electronic submission, validation, refereeing and publication facilities of the journal ensure rapid and high-quality publication of fully validated structures. The primary article category is Research Communications; these are peer-reviewed articles describing one or more structure determinations with appropriate discussion of the science.