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1-(2-Hy­droxy­eth­yl)pyrrole-2,5-dione

The asymmetric unit of the title compound, C(6)H(7)NO(3), contains two mol­ecules (A and B) related by a non-crystallographic twofold pseudo-axis. The mol­ecules are joined in the (AABB)(n) manner by O—H⋯O hydrogen bonds between their hy­droxy groups, thus forming C(2) chains along the a-axis direct...

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Autores principales: Tan, Xue-Jie, Du, Ting-Wen, Xing, Dian-Xiang, Liu, Yun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3343945/
https://www.ncbi.nlm.nih.gov/pubmed/22590026
http://dx.doi.org/10.1107/S1600536812008938
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author Tan, Xue-Jie
Du, Ting-Wen
Xing, Dian-Xiang
Liu, Yun
author_facet Tan, Xue-Jie
Du, Ting-Wen
Xing, Dian-Xiang
Liu, Yun
author_sort Tan, Xue-Jie
collection PubMed
description The asymmetric unit of the title compound, C(6)H(7)NO(3), contains two mol­ecules (A and B) related by a non-crystallographic twofold pseudo-axis. The mol­ecules are joined in the (AABB)(n) manner by O—H⋯O hydrogen bonds between their hy­droxy groups, thus forming C(2) chains along the a-axis direction. Neighboring mol­ecules of the same kind (A and A, or B and B) are related by inversion centers, so that all hy­droxy H atoms are disordered other two sets of sites with half occupancies (superimposed O—H⋯O and O⋯H—O fragments). The mol­ecules are further linked by C—H⋯O inter­actions, which can be considered to be weak hydrogen bonds.
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spelling pubmed-33439452012-05-15 1-(2-Hy­droxy­eth­yl)pyrrole-2,5-dione Tan, Xue-Jie Du, Ting-Wen Xing, Dian-Xiang Liu, Yun Acta Crystallogr Sect E Struct Rep Online Organic Papers The asymmetric unit of the title compound, C(6)H(7)NO(3), contains two mol­ecules (A and B) related by a non-crystallographic twofold pseudo-axis. The mol­ecules are joined in the (AABB)(n) manner by O—H⋯O hydrogen bonds between their hy­droxy groups, thus forming C(2) chains along the a-axis direction. Neighboring mol­ecules of the same kind (A and A, or B and B) are related by inversion centers, so that all hy­droxy H atoms are disordered other two sets of sites with half occupancies (superimposed O—H⋯O and O⋯H—O fragments). The mol­ecules are further linked by C—H⋯O inter­actions, which can be considered to be weak hydrogen bonds. International Union of Crystallography 2012-03-07 /pmc/articles/PMC3343945/ /pubmed/22590026 http://dx.doi.org/10.1107/S1600536812008938 Text en © Tan et al. 2012 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Organic Papers
Tan, Xue-Jie
Du, Ting-Wen
Xing, Dian-Xiang
Liu, Yun
1-(2-Hy­droxy­eth­yl)pyrrole-2,5-dione
title 1-(2-Hy­droxy­eth­yl)pyrrole-2,5-dione
title_full 1-(2-Hy­droxy­eth­yl)pyrrole-2,5-dione
title_fullStr 1-(2-Hy­droxy­eth­yl)pyrrole-2,5-dione
title_full_unstemmed 1-(2-Hy­droxy­eth­yl)pyrrole-2,5-dione
title_short 1-(2-Hy­droxy­eth­yl)pyrrole-2,5-dione
title_sort 1-(2-hy­droxy­eth­yl)pyrrole-2,5-dione
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3343945/
https://www.ncbi.nlm.nih.gov/pubmed/22590026
http://dx.doi.org/10.1107/S1600536812008938
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