e,e-trans-Cyclo­hexane-1,4-carb­oxy­lic acid–hexa­methyl­ene­tetra­mine (1/2)

The asymmetric unit of the title compound, 2C(6)H(12)N(4)·C(8)H(12)O(4), contains one half-mol­ecule of e,e-trans-cyclo­hexane-1,4-dicarb­oxy­lic acid (the complete molecule being generated by inversion symmetry) and one mol­ecule of hexa­methyl­ene­tetra­mine (HMTA), which are connected by O—H⋯N hy...

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Detalles Bibliográficos
Autor principal: Lemmerer, Andreas
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051586/
https://www.ncbi.nlm.nih.gov/pubmed/21522942
http://dx.doi.org/10.1107/S1600536810053626
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author Lemmerer, Andreas
author_facet Lemmerer, Andreas
author_sort Lemmerer, Andreas
collection PubMed
description The asymmetric unit of the title compound, 2C(6)H(12)N(4)·C(8)H(12)O(4), contains one half-mol­ecule of e,e-trans-cyclo­hexane-1,4-dicarb­oxy­lic acid (the complete molecule being generated by inversion symmetry) and one mol­ecule of hexa­methyl­ene­tetra­mine (HMTA), which are connected by O—H⋯N hydrogen bonds. This forms isolated trimers that pack in a herringbone fashion.
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spelling pubmed-30515862011-04-26 e,e-trans-Cyclo­hexane-1,4-carb­oxy­lic acid–hexa­methyl­ene­tetra­mine (1/2) Lemmerer, Andreas Acta Crystallogr Sect E Struct Rep Online Organic Papers The asymmetric unit of the title compound, 2C(6)H(12)N(4)·C(8)H(12)O(4), contains one half-mol­ecule of e,e-trans-cyclo­hexane-1,4-dicarb­oxy­lic acid (the complete molecule being generated by inversion symmetry) and one mol­ecule of hexa­methyl­ene­tetra­mine (HMTA), which are connected by O—H⋯N hydrogen bonds. This forms isolated trimers that pack in a herringbone fashion. International Union of Crystallography 2011-01-08 /pmc/articles/PMC3051586/ /pubmed/21522942 http://dx.doi.org/10.1107/S1600536810053626 Text en © Andreas Lemmerer 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
Lemmerer, Andreas
e,e-trans-Cyclo­hexane-1,4-carb­oxy­lic acid–hexa­methyl­ene­tetra­mine (1/2)
title e,e-trans-Cyclo­hexane-1,4-carb­oxy­lic acid–hexa­methyl­ene­tetra­mine (1/2)
title_full e,e-trans-Cyclo­hexane-1,4-carb­oxy­lic acid–hexa­methyl­ene­tetra­mine (1/2)
title_fullStr e,e-trans-Cyclo­hexane-1,4-carb­oxy­lic acid–hexa­methyl­ene­tetra­mine (1/2)
title_full_unstemmed e,e-trans-Cyclo­hexane-1,4-carb­oxy­lic acid–hexa­methyl­ene­tetra­mine (1/2)
title_short e,e-trans-Cyclo­hexane-1,4-carb­oxy­lic acid–hexa­methyl­ene­tetra­mine (1/2)
title_sort e,e-trans-cyclo­hexane-1,4-carb­oxy­lic acid–hexa­methyl­ene­tetra­mine (1/2)
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051586/
https://www.ncbi.nlm.nih.gov/pubmed/21522942
http://dx.doi.org/10.1107/S1600536810053626
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