Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12323/8165
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dc.contributor.authorShelukho, Evgeniya R-
dc.contributor.authorZaytsev, Vladimir P.-
dc.contributor.authorKhrustalev, Victor N.-
dc.contributor.authorHökelek, Tuncer-
dc.contributor.authorHasanov, Khudayar I.-
dc.contributor.authorGuliyeva, Narmina A.-
dc.contributor.authorJavadzade, Tahir A.-
dc.contributor.authorHadi Al-Douhg, Mohammed-
dc.date.accessioned2025-11-27T08:26:05Z-
dc.date.available2025-11-27T08:26:05Z-
dc.date.issued2025-10-
dc.identifier.issn2056-9890-
dc.identifier.urihttp://hdl.handle.net/20.500.12323/8165-
dc.description.abstractIn the title compound, C17H11NO3S, the thieno[2,3-f]isoindole ring system and the phenyl ring are oriented at a dihedral angle of 20.57 (13)°. The strong intramolecular O—H⋯O hydrogen bond partly ensures the coplanarity of the carboxyl group and the ring system. In crystal, the molecules are linked through C—H⋯O hydrogen bonds, enclosing R²2(14) ring motifs, into a three-dimensional architecture. π–π interactions between parallel five-membered and phenyl rings [centroid-to-centroid distances of 3.564 (3) and 3.591 (3) Å] further contribute to the cohesion of the crystal structure. The Hirshfeld surface analysis indicates that the most important contributions for the crystal packing are from H⋯H (35.5%), H⋯O/O⋯H (21.3%), C⋯C (14.1%) and H⋯C/C⋯H (12.8%) interactions.en_US
dc.language.isoenen_US
dc.publisherInternational Union of Crystallographyen_US
dc.relation.ispartofseriesVol. 81;Acta Crystallographica Section E, Crystallographic Communications, № 11-
dc.subjectintramolecular didehydro-Diels– Alder reactionen_US
dc.subjectpropargylamineen_US
dc.subjectIMDDA reactionen_US
dc.subjectthieno[2,3-f]isoindoleen_US
dc.subjectcrystal structureen_US
dc.titleSynthesis, crystal structure and Hirshfeld surface analysis of 7-oxo-6-phenyl-6,7-dihydro-5H-thieno- [2,3-f]isoindole-8-carboxylic aciden_US
dc.typeArticleen_US
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