(<i>E</i>)-1-(2-Hydroxyphenyl)-3-(3-methoxyphenyl)prop-2-en-1-one

In the title compound, C<sub>16</sub>H<sub>14</sub>O<sub>3</sub>, the phenyl rings are oriented at a dihedral angle of 3.82 (3)° and an intra-molecular O-H⋯O hydrogen bond closes an <i>S</i>(6) ring. In the crystal, weak C-H⋯O and C-H⋯π hydrogen bonds and aromatic π-π stacking occurs. A Hirshfeld surface analysis of the crystal structure indicates that the most important contributions for the crystal packing are from H⋯H (48.2%), H⋯O/O⋯H (20.0%), H⋯C/C⋯H (16.5%) and C⋯C (12.7%) inter-actions.

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IUCrData
Published
2025-03-04
DOI
https://doi.org/10.1107/s2414314625001828
Primary Topic
Crystal structures of chemical compounds
Type
article
Field-Weighted Citation Impact
0.00

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article

(E)-1-(2-Hydroxyphenyl)-3-(3-methoxyphenyl)prop-2-en-1-one

Victor N. Khrustalev, I. G. Mamedov, Alebel N. Belay, Farid N. Naghiyev et al.
IUCrData
Crystal structures of chemical compounds
article

(E)-1-(2-Hydroxyphenyl)-3-(3-methoxyphenyl)prop-2-en-1-one

Victor N. Khrustalev, I. G. Mamedov, Alebel N. Belay, Farid N. Naghiyev, Tuncer Hökelek, Anna Y. Zueva, Kh. A. Asadov
article en

Abstract

In the title compound, C<sub>16</sub>H<sub>14</sub>O<sub>3</sub>, the phenyl rings are oriented at a dihedral angle of 3.82 (3)° and an intra-molecular O-H⋯O hydrogen bond closes an <i>S</i>(6) ring. In the crystal, weak C-H⋯O and C-H⋯π hydrogen bonds and aromatic π-π stacking occurs. A Hirshfeld surface analysis of the crystal structure indicates that the most important contributions for the crystal packing are from H⋯H (48.2%), H⋯O/O⋯H (20.0%), H⋯C/C⋯H (16.5%) and C⋯C (12.7%) inter-actions.

IUCrDataVol. 10(3)
Peoples' Friendship University of Russia (RU), Baku State University (AZ), N.D. Zelinsky Institute of Organic Chemistry (RU), Bahir Dar University (ET), Hacettepe University (TR)
Baki Dövlət Universiteti
Clean water and sanitation
Openalex Percentile: Top 97%
Crystal structures of chemical compounds
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