Abraham Colin-Molina , Jannet Cruz-de la Cruz , David Corona-Becerril , Minerva Rentería-Ortega , Rigoberto Barrios-Francisco
{"title":"Engineering perfluoroarene-arene interactions in coumarin-1,2,3-triazole-arene hybrid molecules","authors":"Abraham Colin-Molina , Jannet Cruz-de la Cruz , David Corona-Becerril , Minerva Rentería-Ortega , Rigoberto Barrios-Francisco","doi":"10.1016/j.jfluchem.2025.110453","DOIUrl":null,"url":null,"abstract":"<div><div>In this work, we describe the synthesis and characterization of five hybrid molecules combining coumarin, 1,2,3-triazole, and arene or perfluoroarene units (compounds <strong>5a, 5b, 6a, 6b</strong>, and <strong>7</strong>). Crystallization conditions of these compounds were explored, and single crystals of compounds <strong>5b</strong> and <strong>7</strong> (as a dioxane solvate, <strong>7<sup>.</sup>DIOX)</strong> were obtained. X-ray diffraction analysis revealed the presence of perfluoroarene–arene (ArF···Ar) interactions that govern the solid-state packing of both structures, leading to rod-like stacking in <strong>5b</strong> and layered arrays in <strong>7·DIOX</strong>. The ArF···Ar contacts were associated with centroid-to-centroid distances between 3.8 and 4.1 Å. Thermal analysis (TGA-DSC) confirmed that all compounds maintain structural integrity at high temperatures; <strong>7·DIOX</strong> retained its crystallinity up to 150 °C before solvent loss. Powder X-ray diffraction confirmed the formation of pure crystalline phases under the employed recrystallization conditions. Additionally, preliminary solid-state fluorescence studies showed modest emission for all coumarin-containing compounds (<strong>5a, 5b</strong>, and <strong>7·DIOX</strong>), with red-shifted maxima and variable quantum yields potentially influenced by non-covalent interactions in their molecular packing. These results underscore the utility of perfluoroarene–arene interactions in directing solid-state organization in fluorinated hybrid molecules.</div></div>","PeriodicalId":357,"journal":{"name":"Journal of Fluorine Chemistry","volume":"285 ","pages":"Article 110453"},"PeriodicalIF":1.7000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Fluorine Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S002211392500065X","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0
Abstract
In this work, we describe the synthesis and characterization of five hybrid molecules combining coumarin, 1,2,3-triazole, and arene or perfluoroarene units (compounds 5a, 5b, 6a, 6b, and 7). Crystallization conditions of these compounds were explored, and single crystals of compounds 5b and 7 (as a dioxane solvate, 7.DIOX) were obtained. X-ray diffraction analysis revealed the presence of perfluoroarene–arene (ArF···Ar) interactions that govern the solid-state packing of both structures, leading to rod-like stacking in 5b and layered arrays in 7·DIOX. The ArF···Ar contacts were associated with centroid-to-centroid distances between 3.8 and 4.1 Å. Thermal analysis (TGA-DSC) confirmed that all compounds maintain structural integrity at high temperatures; 7·DIOX retained its crystallinity up to 150 °C before solvent loss. Powder X-ray diffraction confirmed the formation of pure crystalline phases under the employed recrystallization conditions. Additionally, preliminary solid-state fluorescence studies showed modest emission for all coumarin-containing compounds (5a, 5b, and 7·DIOX), with red-shifted maxima and variable quantum yields potentially influenced by non-covalent interactions in their molecular packing. These results underscore the utility of perfluoroarene–arene interactions in directing solid-state organization in fluorinated hybrid molecules.
期刊介绍:
The Journal of Fluorine Chemistry contains reviews, original papers and short communications. The journal covers all aspects of pure and applied research on the chemistry as well as on the applications of fluorine, and of compounds or materials where fluorine exercises significant effects. This can include all chemistry research areas (inorganic, organic, organometallic, macromolecular and physical chemistry) but also includes papers on biological/biochemical related aspects of Fluorine chemistry as well as medicinal, agrochemical and pharmacological research. The Journal of Fluorine Chemistry also publishes environmental and industrial papers dealing with aspects of Fluorine chemistry on energy and material sciences. Preparative and physico-chemical investigations as well as theoretical, structural and mechanistic aspects are covered. The Journal, however, does not accept work of purely routine nature.
For reviews and special issues on particular topics of fluorine chemistry or from selected symposia, please contact the Regional Editors for further details.