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Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12128/13451
Title: Interactions in flavanone and chalcone derivatives: Hirshfeld surface analysis, energy frameworks and global reactivity descriptors
Authors: Małecka, Magdalena
Chęcińska, Lilianna
Kusz, Joachim
Biernacka, Marta
Kupcewicz, Bogumiła
Keywords: chalcone; crystal structure; energy framework; flavanone; global reactivity descriptor; intermolecular interaction energy; packing
Issue Date: 2020
Citation: “Acta Crystallographica Section C. Structural Chemistry” Vol. 76 (2020), s. 212-224
Abstract: The present study examines a series of flavanone and chalcone derivatives substituted with electron-withdrawing groups (Cl or Br) and electron-donating groups (OH, CH3 and OCH3), namely, 7-methoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one, C16H14O3, 2-(4-methoxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-one, C16H14O3, 2-(4-methoxyphenyl)-6-methyl-3,4-dihydro-2H-1-benzopyran-4-one, C17H16O3, 2-(4-chlorophenyl)-3,4-dihydro-2H-1-benzopyran-4-one, C15H11ClO2, 8-bromo-6-methyl-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one, C16H13BrO2, (2E)-1-(2-hydroxyphenyl)-3-(4-methoxyphenyl)prop-2-en-1-one, C16H14O3, and (2E)-1-(2-hydroxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one, C15H12O3. It compares the two groups of derivatives with regard to their intermolecular interactions in the crystal lattice and lattice energy calculations, together with energy framework visualization and global reactivity descriptors (chemical hardness, chemical potential and electrophilicity index). It also discusses the relationships between different noncovalent interactions derived from Hirshfeld surface analysis, crystal lattice energy and global reactivity descriptors of the compounds.
URI: http://hdl.handle.net/20.500.12128/13451
DOI: 10.1107/S2053229620001503
ISSN: 2053-2296
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