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1,2-Di-4-pyridylethane N,N′-dioxide–acetic acid (1/2)

The title compound, C(12)H(12)N(2)O(2)·2C(2)H(4)O(2), was prepared from 1,2-di-4-pyridylethane, acetic acid, and hydrogen peroxide. The 1,2-di-4-pyridylethane N,N′-dioxide mol­ecule is located on an inversion center. π–π stacking inter­actions between neighboring 1,2-di-4-pyridylethane N,N′-dioxide...

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Detalles Bibliográficos
Autores principales: Boron, Elaine P., Knaust, Jacqueline M.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2972023/
https://www.ncbi.nlm.nih.gov/pubmed/21578711
http://dx.doi.org/10.1107/S1600536809044912
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author Boron, Elaine P.
Knaust, Jacqueline M.
author_facet Boron, Elaine P.
Knaust, Jacqueline M.
author_sort Boron, Elaine P.
collection PubMed
description The title compound, C(12)H(12)N(2)O(2)·2C(2)H(4)O(2), was prepared from 1,2-di-4-pyridylethane, acetic acid, and hydrogen peroxide. The 1,2-di-4-pyridylethane N,N′-dioxide mol­ecule is located on an inversion center. π–π stacking inter­actions between neighboring 1,2-di-4-pyridylethane N,N′-dioxide mol­ecules are observed with a centroid–centroid distance of 3.613 Å, an inter­planar distance of 3.317 Å, and a slippage of 1.433 Å. O—H⋯O hydrogen-bonding inter­actions between 1,2-di-4-pyridylethane N,N′-dioxide and acetic acid mol­ecules result in distinct hydrogen-bonded units made of one N-oxide and two acetic acid mol­ecules. These units are then linked into a three-dimensional network through weaker C—H⋯O hydrogen-bonding inter­actions.
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spelling pubmed-29720232010-12-30 1,2-Di-4-pyridylethane N,N′-dioxide–acetic acid (1/2) Boron, Elaine P. Knaust, Jacqueline M. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(12)H(12)N(2)O(2)·2C(2)H(4)O(2), was prepared from 1,2-di-4-pyridylethane, acetic acid, and hydrogen peroxide. The 1,2-di-4-pyridylethane N,N′-dioxide mol­ecule is located on an inversion center. π–π stacking inter­actions between neighboring 1,2-di-4-pyridylethane N,N′-dioxide mol­ecules are observed with a centroid–centroid distance of 3.613 Å, an inter­planar distance of 3.317 Å, and a slippage of 1.433 Å. O—H⋯O hydrogen-bonding inter­actions between 1,2-di-4-pyridylethane N,N′-dioxide and acetic acid mol­ecules result in distinct hydrogen-bonded units made of one N-oxide and two acetic acid mol­ecules. These units are then linked into a three-dimensional network through weaker C—H⋯O hydrogen-bonding inter­actions. International Union of Crystallography 2009-11-04 /pmc/articles/PMC2972023/ /pubmed/21578711 http://dx.doi.org/10.1107/S1600536809044912 Text en © Boron and Knaust 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
Boron, Elaine P.
Knaust, Jacqueline M.
1,2-Di-4-pyridylethane N,N′-dioxide–acetic acid (1/2)
title 1,2-Di-4-pyridylethane N,N′-dioxide–acetic acid (1/2)
title_full 1,2-Di-4-pyridylethane N,N′-dioxide–acetic acid (1/2)
title_fullStr 1,2-Di-4-pyridylethane N,N′-dioxide–acetic acid (1/2)
title_full_unstemmed 1,2-Di-4-pyridylethane N,N′-dioxide–acetic acid (1/2)
title_short 1,2-Di-4-pyridylethane N,N′-dioxide–acetic acid (1/2)
title_sort 1,2-di-4-pyridylethane n,n′-dioxide–acetic acid (1/2)
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2972023/
https://www.ncbi.nlm.nih.gov/pubmed/21578711
http://dx.doi.org/10.1107/S1600536809044912
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