Naphthalene-1,4,5,8-tetra­carboxylic acid 1,8-anhydride–4,4′-bipyridine (1/1)

The title compound, C(14)H(6)O(7)·C(10)H(8)N(2), has been hydro­thermally synthesized. Structural ananlysis indicates that the crystals are produced by cocrystallization of naphthalene-1,4,5,8-tetra­carboxylic acid 1,8-anhydride and 4,4′-bipyridine (bpy) mol­ecules. The crystal packing is stabilized...

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Autores principales: Deng, Ji-Hua, Guo, Meng-Ping, Zhang, Qiao-Chu, Yuan, Lin, Guo, Hui-Rui, Mei, Guang-Quan
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2970960/
https://www.ncbi.nlm.nih.gov/pubmed/21578491
http://dx.doi.org/10.1107/S1600536809044146
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author Deng, Ji-Hua
Guo, Meng-Ping
Zhang, Qiao-Chu
Yuan, Lin
Guo, Hui-Rui
Mei, Guang-Quan
author_facet Deng, Ji-Hua
Guo, Meng-Ping
Zhang, Qiao-Chu
Yuan, Lin
Guo, Hui-Rui
Mei, Guang-Quan
author_sort Deng, Ji-Hua
collection PubMed
description The title compound, C(14)H(6)O(7)·C(10)H(8)N(2), has been hydro­thermally synthesized. Structural ananlysis indicates that the crystals are produced by cocrystallization of naphthalene-1,4,5,8-tetra­carboxylic acid 1,8-anhydride and 4,4′-bipyridine (bpy) mol­ecules. The crystal packing is stabilized by inter­molecular O—H⋯N and C—H⋯O hydrogen bonds and π–π stacking inter­actions [centroid–centroid distances = 3.5846 (9) Å].
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spelling pubmed-29709602010-12-30 Naphthalene-1,4,5,8-tetra­carboxylic acid 1,8-anhydride–4,4′-bipyridine (1/1) Deng, Ji-Hua Guo, Meng-Ping Zhang, Qiao-Chu Yuan, Lin Guo, Hui-Rui Mei, Guang-Quan Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(14)H(6)O(7)·C(10)H(8)N(2), has been hydro­thermally synthesized. Structural ananlysis indicates that the crystals are produced by cocrystallization of naphthalene-1,4,5,8-tetra­carboxylic acid 1,8-anhydride and 4,4′-bipyridine (bpy) mol­ecules. The crystal packing is stabilized by inter­molecular O—H⋯N and C—H⋯O hydrogen bonds and π–π stacking inter­actions [centroid–centroid distances = 3.5846 (9) Å]. International Union of Crystallography 2009-10-31 /pmc/articles/PMC2970960/ /pubmed/21578491 http://dx.doi.org/10.1107/S1600536809044146 Text en © Deng 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
Deng, Ji-Hua
Guo, Meng-Ping
Zhang, Qiao-Chu
Yuan, Lin
Guo, Hui-Rui
Mei, Guang-Quan
Naphthalene-1,4,5,8-tetra­carboxylic acid 1,8-anhydride–4,4′-bipyridine (1/1)
title Naphthalene-1,4,5,8-tetra­carboxylic acid 1,8-anhydride–4,4′-bipyridine (1/1)
title_full Naphthalene-1,4,5,8-tetra­carboxylic acid 1,8-anhydride–4,4′-bipyridine (1/1)
title_fullStr Naphthalene-1,4,5,8-tetra­carboxylic acid 1,8-anhydride–4,4′-bipyridine (1/1)
title_full_unstemmed Naphthalene-1,4,5,8-tetra­carboxylic acid 1,8-anhydride–4,4′-bipyridine (1/1)
title_short Naphthalene-1,4,5,8-tetra­carboxylic acid 1,8-anhydride–4,4′-bipyridine (1/1)
title_sort naphthalene-1,4,5,8-tetra­carboxylic acid 1,8-anhydride–4,4′-bipyridine (1/1)
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2970960/
https://www.ncbi.nlm.nih.gov/pubmed/21578491
http://dx.doi.org/10.1107/S1600536809044146
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