3-Hydroxy-2-(4-methylphenyl)-4H-chromen-4-one

Our work in the area of carbon-monoxide-releasing molecules led to the synthesis and crystallization of new flavone derivatives as intermediates. Herein we report the first crystal structure of the title compound, C16H12O3, a hydroxy-substituted flavone where the 2-phenyl group has been replaced by...

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Main Authors:	Clifford W. Padgett, Will E. Lynch, Kirkland Sheriff, Raven Dean, Sarah Zingales
Format:	Article
Language:	English
Published:	International Union of Crystallography 2018-08-01
Series:	IUCrData
Subjects:	crystal structure benzopyran flavone hydrogen bond
Online Access:	http://scripts.iucr.org/cgi-bin/paper?S2414314618011380

id	doaj-1f0ff4d4d3024c37bc08f32513f2b3d1
record_format	Article
spelling	doaj-1f0ff4d4d3024c37bc08f32513f2b3d12020-11-24T22:31:23ZengInternational Union of CrystallographyIUCrData2414-31462018-08-0138x18113810.1107/S2414314618011380bh40393-Hydroxy-2-(4-methylphenyl)-4H-chromen-4-oneClifford W. Padgett0Will E. Lynch1Kirkland Sheriff2Raven Dean3Sarah Zingales4Georgia Southern University, 11935 Abercorn St., Department of Chemistry and Biochemistry, Savannah GA 31419, USAGeorgia Southern University, 11935 Abercorn St., Department of Chemistry and Biochemistry, Savannah GA 31419, USAGeorgia Southern University, 11935 Abercorn St., Department of Chemistry and Biochemistry, Savannah GA 31419, USAGeorgia Southern University, 11935 Abercorn St., Department of Chemistry and Biochemistry, Savannah GA 31419, USAGeorgia Southern University, 11935 Abercorn St., Department of Chemistry and Biochemistry, Savannah GA 31419, USAOur work in the area of carbon-monoxide-releasing molecules led to the synthesis and crystallization of new flavone derivatives as intermediates. Herein we report the first crystal structure of the title compound, C16H12O3, a hydroxy-substituted flavone where the 2-phenyl group has been replaced by a p-tolyl group. The introduction of the 3-hydroxy group allows the formation of intermolecular O—H...O=C hydrogen bonds, used to build centrosymmetric R22(10) ring motifs in the crystal.http://scripts.iucr.org/cgi-bin/paper?S2414314618011380crystal structurebenzopyranflavonehydrogen bond
collection	DOAJ
language	English
format	Article
sources	DOAJ
author	Clifford W. Padgett Will E. Lynch Kirkland Sheriff Raven Dean Sarah Zingales
spellingShingle	Clifford W. Padgett Will E. Lynch Kirkland Sheriff Raven Dean Sarah Zingales 3-Hydroxy-2-(4-methylphenyl)-4H-chromen-4-one IUCrData crystal structure benzopyran flavone hydrogen bond
author_facet	Clifford W. Padgett Will E. Lynch Kirkland Sheriff Raven Dean Sarah Zingales
author_sort	Clifford W. Padgett
title	3-Hydroxy-2-(4-methylphenyl)-4H-chromen-4-one
title_short	3-Hydroxy-2-(4-methylphenyl)-4H-chromen-4-one
title_full	3-Hydroxy-2-(4-methylphenyl)-4H-chromen-4-one
title_fullStr	3-Hydroxy-2-(4-methylphenyl)-4H-chromen-4-one
title_full_unstemmed	3-Hydroxy-2-(4-methylphenyl)-4H-chromen-4-one
title_sort	3-hydroxy-2-(4-methylphenyl)-4h-chromen-4-one
publisher	International Union of Crystallography
series	IUCrData
issn	2414-3146
publishDate	2018-08-01
description	Our work in the area of carbon-monoxide-releasing molecules led to the synthesis and crystallization of new flavone derivatives as intermediates. Herein we report the first crystal structure of the title compound, C16H12O3, a hydroxy-substituted flavone where the 2-phenyl group has been replaced by a p-tolyl group. The introduction of the 3-hydroxy group allows the formation of intermolecular O—H...O=C hydrogen bonds, used to build centrosymmetric R22(10) ring motifs in the crystal.
topic	crystal structure benzopyran flavone hydrogen bond
url	http://scripts.iucr.org/cgi-bin/paper?S2414314618011380
work_keys_str_mv	AT cliffordwpadgett 3hydroxy24methylphenyl4hchromen4one AT willelynch 3hydroxy24methylphenyl4hchromen4one AT kirklandsheriff 3hydroxy24methylphenyl4hchromen4one AT ravendean 3hydroxy24methylphenyl4hchromen4one AT sarahzingales 3hydroxy24methylphenyl4hchromen4one
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3-Hydroxy-2-(4-methylphenyl)-4H-chromen-4-one

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