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4,4′-Bipyridine–5-fluoro­isophthalic acid (1/1)

Co-crystallization of 5-fluoro­isophthalic acid (H(2)fip) with 4,4′-bipyridine (bipy) leads to the formation of the title compound [(H(2)fip)(bipy)], C(8)H(5)FO(4)·C(10)H(8)N(2), with an acid–base molar ratio of 1:1. The acid and base subunits are arrange alternately in the crystal structure, displa...

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Detalles Bibliográficos
Autor principal: Qin, Jin-Lai
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052053/
https://www.ncbi.nlm.nih.gov/pubmed/21522350
http://dx.doi.org/10.1107/S1600536811004016
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author Qin, Jin-Lai
author_facet Qin, Jin-Lai
author_sort Qin, Jin-Lai
collection PubMed
description Co-crystallization of 5-fluoro­isophthalic acid (H(2)fip) with 4,4′-bipyridine (bipy) leads to the formation of the title compound [(H(2)fip)(bipy)], C(8)H(5)FO(4)·C(10)H(8)N(2), with an acid–base molar ratio of 1:1. The acid and base subunits are arrange alternately in the crystal structure, displaying a wave-like tape motif via inter­molecular O—H⋯N and C—H⋯O hydrogen bonds [carbox­yl–pyridine synthon of R (2) (2)(7) hydrogen-bond notation], which are further combined into a two-dimensional architecture through C—H⋯F inter­actions involving the bipy and H(2)fip mol­ecules.
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spelling pubmed-30520532011-04-26 4,4′-Bipyridine–5-fluoro­isophthalic acid (1/1) Qin, Jin-Lai Acta Crystallogr Sect E Struct Rep Online Organic Papers Co-crystallization of 5-fluoro­isophthalic acid (H(2)fip) with 4,4′-bipyridine (bipy) leads to the formation of the title compound [(H(2)fip)(bipy)], C(8)H(5)FO(4)·C(10)H(8)N(2), with an acid–base molar ratio of 1:1. The acid and base subunits are arrange alternately in the crystal structure, displaying a wave-like tape motif via inter­molecular O—H⋯N and C—H⋯O hydrogen bonds [carbox­yl–pyridine synthon of R (2) (2)(7) hydrogen-bond notation], which are further combined into a two-dimensional architecture through C—H⋯F inter­actions involving the bipy and H(2)fip mol­ecules. International Union of Crystallography 2011-02-09 /pmc/articles/PMC3052053/ /pubmed/21522350 http://dx.doi.org/10.1107/S1600536811004016 Text en © Jin-Lai Qin 2011 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
Qin, Jin-Lai
4,4′-Bipyridine–5-fluoro­isophthalic acid (1/1)
title 4,4′-Bipyridine–5-fluoro­isophthalic acid (1/1)
title_full 4,4′-Bipyridine–5-fluoro­isophthalic acid (1/1)
title_fullStr 4,4′-Bipyridine–5-fluoro­isophthalic acid (1/1)
title_full_unstemmed 4,4′-Bipyridine–5-fluoro­isophthalic acid (1/1)
title_short 4,4′-Bipyridine–5-fluoro­isophthalic acid (1/1)
title_sort 4,4′-bipyridine–5-fluoro­isophthalic acid (1/1)
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052053/
https://www.ncbi.nlm.nih.gov/pubmed/21522350
http://dx.doi.org/10.1107/S1600536811004016
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