The chalcone derivative (E)-1-(4-fluorophenyl)-3-(4-hydroxy-3-methoxyphenyl)prop-2-en-1-one monohydrate

The chalcone derivative (E)-1-(4-fluorophenyl)-3-(4-hydroxy-3-methoxyphenyl)prop-2-en-1-one monohydrate

The title compound, C16H13FO3·H2O, has a cis disposition of the carbonyl and olefin bonds about the enone single bond. The arene rings are inclined to one another by 10.05 (6) Å. In the crystal, molecules are linked via O—H...O hydrogen bonds involving...

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Main Authors: Florastina Payton-Stewart, Subramanya Ravi Kiran Pingali, James P. Donahue
Format: Article
Language:English
Published: International Union of Crystallography 2013-04-01
Series:Acta Crystallographica Section E
Online Access:http://scripts.iucr.org/cgi-bin/paper?S160053681300696X
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spelling doaj-c4b6e9685d834b0f9f8cf262cc69ce282020-11-25T02:24:22ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682013-04-01694o558o55910.1107/S160053681300696XThe chalcone derivative (E)-1-(4-fluorophenyl)-3-(4-hydroxy-3-methoxyphenyl)prop-2-en-1-one monohydrateFlorastina Payton-StewartSubramanya Ravi Kiran PingaliJames P. DonahueThe title compound, C16H13FO3·H2O, has a cis disposition of the carbonyl and olefin bonds about the enone single bond. The arene rings are inclined to one another by 10.05 (6) Å. In the crystal, molecules are linked via O—H...O hydrogen bonds involving the water molecules, forming loops which are, in turn, linked via O—H.·O and C—H...F hydrogen bonds, forming sheets lying parallel to (103). These networks are linked via π–π interactions [centroid–centroid distance = 3.641 (1) Å] involving inversion-related 4-fluorophenyl and 4-hydroxy-3-methoxyphenyl rings.http://scripts.iucr.org/cgi-bin/paper?S160053681300696X
collection DOAJ
language English
format Article
sources DOAJ
author Florastina Payton-Stewart
Subramanya Ravi Kiran Pingali
James P. Donahue
spellingShingle Florastina Payton-Stewart
Subramanya Ravi Kiran Pingali
James P. Donahue
The chalcone derivative (E)-1-(4-fluorophenyl)-3-(4-hydroxy-3-methoxyphenyl)prop-2-en-1-one monohydrate
Acta Crystallographica Section E
author_facet Florastina Payton-Stewart
Subramanya Ravi Kiran Pingali
James P. Donahue
author_sort Florastina Payton-Stewart
title The chalcone derivative (E)-1-(4-fluorophenyl)-3-(4-hydroxy-3-methoxyphenyl)prop-2-en-1-one monohydrate
title_short The chalcone derivative (E)-1-(4-fluorophenyl)-3-(4-hydroxy-3-methoxyphenyl)prop-2-en-1-one monohydrate
title_full The chalcone derivative (E)-1-(4-fluorophenyl)-3-(4-hydroxy-3-methoxyphenyl)prop-2-en-1-one monohydrate
title_fullStr The chalcone derivative (E)-1-(4-fluorophenyl)-3-(4-hydroxy-3-methoxyphenyl)prop-2-en-1-one monohydrate
title_full_unstemmed The chalcone derivative (E)-1-(4-fluorophenyl)-3-(4-hydroxy-3-methoxyphenyl)prop-2-en-1-one monohydrate
title_sort chalcone derivative (e)-1-(4-fluorophenyl)-3-(4-hydroxy-3-methoxyphenyl)prop-2-en-1-one monohydrate
publisher International Union of Crystallography
series Acta Crystallographica Section E
issn 1600-5368
publishDate 2013-04-01
description The title compound, C16H13FO3·H2O, has a cis disposition of the carbonyl and olefin bonds about the enone single bond. The arene rings are inclined to one another by 10.05 (6) Å. In the crystal, molecules are linked via O—H...O hydrogen bonds involving the water molecules, forming loops which are, in turn, linked via O—H.·O and C—H...F hydrogen bonds, forming sheets lying parallel to (103). These networks are linked via π–π interactions [centroid–centroid distance = 3.641 (1) Å] involving inversion-related 4-fluorophenyl and 4-hydroxy-3-methoxyphenyl rings.
url http://scripts.iucr.org/cgi-bin/paper?S160053681300696X
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