Crystal structure and synthesis of 3-(1H-pyrrol-2-yl)-1-(thiophen-2-yl)propanone

The title compound, C11H9NOS, was obtained in an improved yield compared to previous literature methods. The molecule is essentially planar with a maximum deviation of 0.085 Å from the mean plane through all non-H atoms. There is directive intermolecular hydrogen bonding in the form of N—H...O hydro...

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Main Authors: Dáire Gibbons, Ganapathi Emandi, Mathias O. Senge
Format: Article
Language:English
Published: International Union of Crystallography 2018-10-01
Series:Acta Crystallographica Section E: Crystallographic Communications
Subjects:
Online Access:http://scripts.iucr.org/cgi-bin/paper?S2056989018012331
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spelling doaj-89a21a135e264a3c9a5d45e9272eb8752020-11-25T00:41:05ZengInternational Union of CrystallographyActa Crystallographica Section E: Crystallographic Communications2056-98902018-10-0174101463146610.1107/S2056989018012331tx2008Crystal structure and synthesis of 3-(1H-pyrrol-2-yl)-1-(thiophen-2-yl)propanoneDáire Gibbons0Ganapathi Emandi1Mathias O. Senge2School of Chemistry, Trinity Biomedical Sciences Institute, 152–160 Pearse Street, Trinity College Dublin, The University of Dublin, Dublin 2, IrelandSchool of Chemistry, Trinity Biomedical Sciences Institute, 152–160 Pearse Street, Trinity College Dublin, The University of Dublin, Dublin 2, IrelandSchool of Chemistry, Trinity Biomedical Sciences Institute, 152–160 Pearse Street, Trinity College Dublin, The University of Dublin, Dublin 2, IrelandThe title compound, C11H9NOS, was obtained in an improved yield compared to previous literature methods. The molecule is essentially planar with a maximum deviation of 0.085 Å from the mean plane through all non-H atoms. There is directive intermolecular hydrogen bonding in the form of N—H...O hydrogen bonds with a distance of 2.889 (3) Å between the pyrrole amine and the ketone carbonyl O atom. The resulting hydrogen-bonding network defines a ribbon parallel to the a axis. These ribbons form offset stacks along the b axis.http://scripts.iucr.org/cgi-bin/paper?S2056989018012331crystal structurethiophenepyrroleBODIPYaza-BODIPY
collection DOAJ
language English
format Article
sources DOAJ
author Dáire Gibbons
Ganapathi Emandi
Mathias O. Senge
spellingShingle Dáire Gibbons
Ganapathi Emandi
Mathias O. Senge
Crystal structure and synthesis of 3-(1H-pyrrol-2-yl)-1-(thiophen-2-yl)propanone
Acta Crystallographica Section E: Crystallographic Communications
crystal structure
thiophene
pyrrole
BODIPY
aza-BODIPY
author_facet Dáire Gibbons
Ganapathi Emandi
Mathias O. Senge
author_sort Dáire Gibbons
title Crystal structure and synthesis of 3-(1H-pyrrol-2-yl)-1-(thiophen-2-yl)propanone
title_short Crystal structure and synthesis of 3-(1H-pyrrol-2-yl)-1-(thiophen-2-yl)propanone
title_full Crystal structure and synthesis of 3-(1H-pyrrol-2-yl)-1-(thiophen-2-yl)propanone
title_fullStr Crystal structure and synthesis of 3-(1H-pyrrol-2-yl)-1-(thiophen-2-yl)propanone
title_full_unstemmed Crystal structure and synthesis of 3-(1H-pyrrol-2-yl)-1-(thiophen-2-yl)propanone
title_sort crystal structure and synthesis of 3-(1h-pyrrol-2-yl)-1-(thiophen-2-yl)propanone
publisher International Union of Crystallography
series Acta Crystallographica Section E: Crystallographic Communications
issn 2056-9890
publishDate 2018-10-01
description The title compound, C11H9NOS, was obtained in an improved yield compared to previous literature methods. The molecule is essentially planar with a maximum deviation of 0.085 Å from the mean plane through all non-H atoms. There is directive intermolecular hydrogen bonding in the form of N—H...O hydrogen bonds with a distance of 2.889 (3) Å between the pyrrole amine and the ketone carbonyl O atom. The resulting hydrogen-bonding network defines a ribbon parallel to the a axis. These ribbons form offset stacks along the b axis.
topic crystal structure
thiophene
pyrrole
BODIPY
aza-BODIPY
url http://scripts.iucr.org/cgi-bin/paper?S2056989018012331
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AT mathiasosenge crystalstructureandsynthesisof31hpyrrol2yl1thiophen2ylpropanone
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