2-(2-Hydroxy­ethyl)-3-[(2-hydroxy­ethyl)imino]isoindolin-1-one

In the crystal structure of the title compound, C(12)H(14)N(2)O(3), mol­ecules are packed into layers parallel to (100). Each layer contains centrosymmetric dimers formed by a pair of strong O—H⋯N hydrogen bonds with an R (2) (2)(10) motif, while strong O—H⋯O hydrogen bonds forming C(10) chains conn...

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Detalles Bibliográficos
Autores principales: Urban, Jiří, Ludvík, Jiří, Fábry, Jan, Dušek, Michal, Fejfarová, Karla
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2970005/
https://www.ncbi.nlm.nih.gov/pubmed/21577509
http://dx.doi.org/10.1107/S1600536809030487
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author Urban, Jiří
Ludvík, Jiří
Fábry, Jan
Dušek, Michal
Fejfarová, Karla
author_facet Urban, Jiří
Ludvík, Jiří
Fábry, Jan
Dušek, Michal
Fejfarová, Karla
author_sort Urban, Jiří
collection PubMed
description In the crystal structure of the title compound, C(12)H(14)N(2)O(3), mol­ecules are packed into layers parallel to (100). Each layer contains centrosymmetric dimers formed by a pair of strong O—H⋯N hydrogen bonds with an R (2) (2)(10) motif, while strong O—H⋯O hydrogen bonds forming C(10) chains connect mol­ecules into a two-dimensional network. Additional stabilization is supplied by weak C—H⋯O hydrogen bonds and weak π–π stacking inter­actions with centroid–centroid distances in the range 3.4220 (7)–3.9616 (7) Å.
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spelling pubmed-29700052010-12-30 2-(2-Hydroxy­ethyl)-3-[(2-hydroxy­ethyl)imino]isoindolin-1-one Urban, Jiří Ludvík, Jiří Fábry, Jan Dušek, Michal Fejfarová, Karla Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal structure of the title compound, C(12)H(14)N(2)O(3), mol­ecules are packed into layers parallel to (100). Each layer contains centrosymmetric dimers formed by a pair of strong O—H⋯N hydrogen bonds with an R (2) (2)(10) motif, while strong O—H⋯O hydrogen bonds forming C(10) chains connect mol­ecules into a two-dimensional network. Additional stabilization is supplied by weak C—H⋯O hydrogen bonds and weak π–π stacking inter­actions with centroid–centroid distances in the range 3.4220 (7)–3.9616 (7) Å. International Union of Crystallography 2009-08-08 /pmc/articles/PMC2970005/ /pubmed/21577509 http://dx.doi.org/10.1107/S1600536809030487 Text en © Urban et al. 2009 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
Urban, Jiří
Ludvík, Jiří
Fábry, Jan
Dušek, Michal
Fejfarová, Karla
2-(2-Hydroxy­ethyl)-3-[(2-hydroxy­ethyl)imino]isoindolin-1-one
title 2-(2-Hydroxy­ethyl)-3-[(2-hydroxy­ethyl)imino]isoindolin-1-one
title_full 2-(2-Hydroxy­ethyl)-3-[(2-hydroxy­ethyl)imino]isoindolin-1-one
title_fullStr 2-(2-Hydroxy­ethyl)-3-[(2-hydroxy­ethyl)imino]isoindolin-1-one
title_full_unstemmed 2-(2-Hydroxy­ethyl)-3-[(2-hydroxy­ethyl)imino]isoindolin-1-one
title_short 2-(2-Hydroxy­ethyl)-3-[(2-hydroxy­ethyl)imino]isoindolin-1-one
title_sort 2-(2-hydroxy­ethyl)-3-[(2-hydroxy­ethyl)imino]isoindolin-1-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2970005/
https://www.ncbi.nlm.nih.gov/pubmed/21577509
http://dx.doi.org/10.1107/S1600536809030487
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