Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12323/8165
Title: Synthesis, crystal structure and Hirshfeld surface analysis of 7-oxo-6-phenyl-6,7-dihydro-5H-thieno- [2,3-f]isoindole-8-carboxylic acid
Authors: Shelukho, Evgeniya R
Zaytsev, Vladimir P.
Khrustalev, Victor N.
Hökelek, Tuncer
Hasanov, Khudayar I.
Guliyeva, Narmina A.
Javadzade, Tahir A.
Hadi Al-Douhg, Mohammed
Keywords: intramolecular didehydro-Diels– Alder reaction
propargylamine
IMDDA reaction
thieno[2,3-f]isoindole
crystal structure
Issue Date: Oct-2025
Publisher: International Union of Crystallography
Series/Report no.: Vol. 81;Acta Crystallographica Section E, Crystallographic Communications, № 11
Abstract: In 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.
URI: http://hdl.handle.net/20.500.12323/8165
ISSN: 2056-9890
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