2,2′-(2,2′-Biimidazole-1,1′-di­yl)diethanoic acid

In the title compound, C(10)H(10)N(4)O(4), the two imidazole rings adopt a trans conformation and are inclined to one another at a dihedral angle of 55.64 (4)°. In the crystal structure, mol­ecules are linked by inter­molecular O—H⋯N hydrogen bonds into chains running parallel to [010] and layers ar...

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Detalles Bibliográficos
Autores principales: Zhang, Tingting, Zhang, Tao, Ren, Yingtao, Liang, Hongze
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968835/
https://www.ncbi.nlm.nih.gov/pubmed/21582608
http://dx.doi.org/10.1107/S1600536809010897
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author Zhang, Tingting
Zhang, Tao
Ren, Yingtao
Liang, Hongze
author_facet Zhang, Tingting
Zhang, Tao
Ren, Yingtao
Liang, Hongze
author_sort Zhang, Tingting
collection PubMed
description In the title compound, C(10)H(10)N(4)O(4), the two imidazole rings adopt a trans conformation and are inclined to one another at a dihedral angle of 55.64 (4)°. In the crystal structure, mol­ecules are linked by inter­molecular O—H⋯N hydrogen bonds into chains running parallel to [010] and layers are formed from these by inter­molecular C—H⋯O hydrogen bonds. Additional C—H⋯O hydrogen bonds produce a three-dimensional network.
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spelling pubmed-29688352010-12-30 2,2′-(2,2′-Biimidazole-1,1′-di­yl)diethanoic acid Zhang, Tingting Zhang, Tao Ren, Yingtao Liang, Hongze Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(10)H(10)N(4)O(4), the two imidazole rings adopt a trans conformation and are inclined to one another at a dihedral angle of 55.64 (4)°. In the crystal structure, mol­ecules are linked by inter­molecular O—H⋯N hydrogen bonds into chains running parallel to [010] and layers are formed from these by inter­molecular C—H⋯O hydrogen bonds. Additional C—H⋯O hydrogen bonds produce a three-dimensional network. International Union of Crystallography 2009-03-28 /pmc/articles/PMC2968835/ /pubmed/21582608 http://dx.doi.org/10.1107/S1600536809010897 Text en © Zhang 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
Zhang, Tingting
Zhang, Tao
Ren, Yingtao
Liang, Hongze
2,2′-(2,2′-Biimidazole-1,1′-di­yl)diethanoic acid
title 2,2′-(2,2′-Biimidazole-1,1′-di­yl)diethanoic acid
title_full 2,2′-(2,2′-Biimidazole-1,1′-di­yl)diethanoic acid
title_fullStr 2,2′-(2,2′-Biimidazole-1,1′-di­yl)diethanoic acid
title_full_unstemmed 2,2′-(2,2′-Biimidazole-1,1′-di­yl)diethanoic acid
title_short 2,2′-(2,2′-Biimidazole-1,1′-di­yl)diethanoic acid
title_sort 2,2′-(2,2′-biimidazole-1,1′-di­yl)diethanoic acid
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968835/
https://www.ncbi.nlm.nih.gov/pubmed/21582608
http://dx.doi.org/10.1107/S1600536809010897
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AT zhangtao 2222biimidazole11diyldiethanoicacid
AT renyingtao 2222biimidazole11diyldiethanoicacid
AT lianghongze 2222biimidazole11diyldiethanoicacid

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