Publication:
Crystal Structure and Hirshfeld Surface Analysis of (E)-6-(4-Hydroxy-3-Methoxy-Styryl)-4,5-Dihydro-Pyridazin-3(2H)-one

dc.authorscopusid54410446800
dc.authorscopusid57210190171
dc.authorscopusid57218830426
dc.authorscopusid54883875100
dc.authorscopusid57201620841
dc.authorscopusid55652041800
dc.authorscopusid55652041800
dc.contributor.authorDaoui, S.
dc.contributor.authorBaydere, C.
dc.contributor.authorEl Kalai, F.E.
dc.contributor.authorSaddik, R.
dc.contributor.authorDege, N.
dc.contributor.authorKarrouchi, K.
dc.contributor.authorBenchat, N.
dc.date.accessioned2020-06-21T09:05:20Z
dc.date.available2020-06-21T09:05:20Z
dc.date.issued2019
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Daoui] Said, Université Mohammed Premier Oujda, Oujda, Oriental, Morocco; [Baydere] Cemile, Department of Physics, Ondokuz Mayis University Faculty of Science and Arts, Samsun, Turkey; [El Kalai] Fouad, Université Mohammed Premier Oujda, Oujda, Oriental, Morocco; [Saddik] Rafik, Laboratory for Organic Synthesis Extraction and Valorization, Hassan II University of Casablanca, Casablanca, Casablanca-Settat, Morocco; [Dege] Necmi, Department of Physics, Ondokuz Mayis University Faculty of Science and Arts, Samsun, Turkey; [Karrouchi] Khalid, Laboratory of Plant Chemistry Organic and Bioorganic Synthesis, Faculté des Sciences Rabat, Rabat, Morocco; [Benchat] Noureddine, Université Mohammed Premier Oujda, Oujda, Oriental, Moroccoen_US
dc.description.abstractIn the title compound, C13H14N2O3, the dihydropyridazine ring (r.m.s. deviation = 0.166 Å) has a screw-boat conformation. The dihedral angle between its mean plane and the benzene ring is 0.77 (12)°. In the crystal, intermolecular O-H..O hydrogen bonds generate C(5) chains and N-H..O hydrogen bonds produce R 2 2(8) motifs. These types of interactions lead to the formation of layers parallel to (12). The three-dimensional network is achieved by C-H..O interactions, including R 2 4(8) motifs. Intermolecular interactions were additionally investigated using Hirshfeld surface analysis and two-dimensional fingerprint plots. The most significant contributions to the crystal packing are by H..H (43.3%), H..C/C..H (19.3%), H..O/H..O (22.6%), C..N/N..C (3.0%) and H..N/N..H (5.8%) contacts. C-H..π interactions and aromatic π-π stacking interactions are not observed. © 2019 International Union of Crystallography. All rights reserved.en_US
dc.identifier.doi10.1107/S2056989019014130
dc.identifier.endpage1737en_US
dc.identifier.issn2056-9890
dc.identifier.scopus2-s2.0-85074800581
dc.identifier.scopusqualityQ3
dc.identifier.startpage1734en_US
dc.identifier.urihttps://doi.org/10.1107/S2056989019014130
dc.identifier.volume75en_US
dc.language.isoenen_US
dc.publisherInternational Union of Crystallography 5 Abbey Square Chester CH1 2HUen_US
dc.relation.ispartofActa Crystallographica Section E-Crystallographic Communicationsen_US
dc.relation.journalActa Crystallographica Section E: Crystallographic Communicationsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectCrystal Structureen_US
dc.subjectHirshfeld Surface Analysisen_US
dc.subjectHydrogen Bondingen_US
dc.subjectPyridazineen_US
dc.titleCrystal Structure and Hirshfeld Surface Analysis of (E)-6-(4-Hydroxy-3-Methoxy-Styryl)-4,5-Dihydro-Pyridazin-3(2H)-oneen_US
dc.typeArticleen_US
dspace.entity.typePublication

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