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dc.contributor.authorSuchojad, Kamil
dc.contributor.authorMałecka, Magdalena
dc.contributor.authorAdamus-Grabicka, Angelika
dc.contributor.authorBudzisz, Elżbieta
dc.contributor.authorDołęga, Anna
dc.date.accessioned2022-01-26T18:49:27Z
dc.date.available2022-01-26T18:49:27Z
dc.date.issued2019
dc.identifier.issn2056-9890
dc.identifier.urihttp://hdl.handle.net/11089/40505
dc.descriptionThe synthesis and crystal structures of (E)-3-(4-hy­droxy­benzyl­idene)chroman-4-one, C16H12O3, I, and (E)-3-(3-hy­droxy­benzyl­idene)-2-phenyl­chroman-4-one, C22H16O3, II, are reported. These compounds are of inter­est with respect to biological activity. Both structures display inter­molecular C—H⋯O and O—H⋯O hydrogen bonding, forming layers in the crystal lattice. The crystal structure of compound I is consolidated by π–π inter­actions. The lipophilicity (logP) was determined as it is one of the parameters qualifying compounds as potential drugs. The logP value for compound I is associated with a larger contribution of C⋯H inter­action in the Hirshfeld surface.pl_PL
dc.description.sponsorshipFunding for this research was provided by: Uniwesytet Łódzki, Uniwersytet Medyczny w Łodzi (grant No. SGB_148_Suchojad_Kamil to K. Suchojad; grant No. 502-03/3-066-02/502-34-118 to A. Adamus-Grabicka, E. Budzisz).pl_PL
dc.language.isoenpl_PL
dc.publisherInternational Union of Crystallographypl_PL
dc.relation.ispartofseriesActa Crystallographica Section E: Crystallographic Communications;75
dc.rightsUznanie autorstwa 4.0 Międzynarodowe*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectcrystal structurepl_PL
dc.subjectchromanone derivativepl_PL
dc.subjectflavanone derivativepl_PL
dc.subjectlipophilicity indexpl_PL
dc.subjectHirshfeld surface analysispl_PL
dc.titleCrystal structures of (E)-3-(4-hy­dr­oxy­benzyl­­idene)chroman-4-one and (E)-3-(3-hy­dr­oxy­benzyl­­idene)-2-phenyl­chroman-4-onepl_PL
dc.typeArticlepl_PL
dc.page.number1907-1913pl_PL
dc.contributor.authorAffiliationDepartment of Physical Chemistry, Faculty of Chemistry, University of Lodz, Pomorska 163/165, 90-236 Łódź, Polandpl_PL
dc.contributor.authorAffiliationDepartment of Physical Chemistry, Faculty of Chemistry, University of Lodz, Pomorska 163/165, 90-236 Łódź, Polandpl_PL
dc.contributor.authorAffiliationDepartment of Inorganic Chemistry, Gdańsk University of Technology, G. Narutowicza 11/12., 80-233 Gdańsk, Polandpl_PL
dc.contributor.authorAffiliationDepartment of Cosmetic Raw Materials Chemistry, Faculty of Pharmacy, Medical University of Lodz, Muszynskiego 1, 90-151 Łódź, Polandpl_PL
dc.contributor.authorAffiliationDepartment of Cosmetic Raw Materials Chemistry, Faculty of Pharmacy, Medical University of Lodz, Muszynskiego 1, 90-151 Łódź, Polandpl_PL
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dc.contributor.authorEmailmagdalena.malecka@chemia.uni.lodz.plpl_PL
dc.identifier.doi10.1107/S2056989019015639
dc.relation.volume12pl_PL
dc.disciplinenauki chemicznepl_PL


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