Crystal structure, mosquito larvicidal & antifungal activity of 3‑tert‑butyl‑7-(2,3,4-trimethoxyphenyl)-4H-[1,3,4]thiadiazolo[2,3-c][1,2,4]triazin-4-one

•Single crystal was grown using slow evaporation technique.•Crystal possesses orthorhombic system with space group Pbca.•The percentage of intermolecular contacts was resolved by hirshfeld surface analyses.•The compound (5) was screened for its antifungal and mosquito larvicidal activity. The title...

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Veröffentlicht in:Journal of molecular structure 2021-09, Vol.1240, p.130504, Article 130504
Hauptverfasser: J, Chandraprabha V., Dasappa, Jagadeesh Prasad, H, Gayathri B., S, Madan Kumar, Shivarama Holla, B., Kamble, Ravindra R., Naik, Prashantha
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Sprache:eng
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Zusammenfassung:•Single crystal was grown using slow evaporation technique.•Crystal possesses orthorhombic system with space group Pbca.•The percentage of intermolecular contacts was resolved by hirshfeld surface analyses.•The compound (5) was screened for its antifungal and mosquito larvicidal activity. The title compound 3‑tert‑butyl‑7-(2,3,4-trimethoxyphenyl)-4H-[1,3,4]thiadiazolo[2,3-c][1,2,4]triazin-4-one was prepared and characterized using single crystal X-ray diffraction, thermal & Uv-Vis analysis, FTIR, NMR (1H, 13C) and Mass spectral studies. The intercontacts in the crystal structure were analyzed and quantified using Hirshfeld surfaces computational method. Intermolecular hydrogen bonds C12—H12A…O4, C13—H13C…O4, C15—H15A…O2 and C16—H16B…O3 connects the molecule in the crystal structure. The intramolecular hydrogen bond of the type C—H …N was observed. Intercontacts H…H, O… H and N…H shows more contributions towards Hirshfeld surfaces. Thermal analysis indicates the title compound starts to degrade at 216.9 °C. In addition, mosquito larvicidal activity and antifungal activity were performed.
ISSN:0022-2860
1872-8014
DOI:10.1016/j.molstruc.2021.130504