4,4′,6,6′-Tetra­methyl-2,2′-bipyrimidine hexa­hydrate

In the title compound, C(12)H(14)N(4)·6H(2)O, the two pyrimidine rings make a dihedral angle of 5.285 (6)°. Inter­molecular O—H⋯O hydrogen bonds link the six water mol­ecules, generating edge-fused four-, five- or six-membered ring motifs and forming two-dimensional sheets. The sheets are stabilized...

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Detalles Bibliográficos
Autores principales: Ma, Yanni, Zhou, Le, Deng, Dongsheng, Ji, Baoming
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968866/
https://www.ncbi.nlm.nih.gov/pubmed/21582567
http://dx.doi.org/10.1107/S1600536809010095
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author Ma, Yanni
Zhou, Le
Deng, Dongsheng
Ji, Baoming
author_facet Ma, Yanni
Zhou, Le
Deng, Dongsheng
Ji, Baoming
author_sort Ma, Yanni
collection PubMed
description In the title compound, C(12)H(14)N(4)·6H(2)O, the two pyrimidine rings make a dihedral angle of 5.285 (6)°. Inter­molecular O—H⋯O hydrogen bonds link the six water mol­ecules, generating edge-fused four-, five- or six-membered ring motifs and forming two-dimensional sheets. The sheets are stabilized by the formation of O—H⋯N hydrogen bonds between the water mol­ecules and the bipyrimidine mol­ecules, resulting in a three-dimensional network.
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spelling pubmed-29688662010-12-30 4,4′,6,6′-Tetra­methyl-2,2′-bipyrimidine hexa­hydrate Ma, Yanni Zhou, Le Deng, Dongsheng Ji, Baoming Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(12)H(14)N(4)·6H(2)O, the two pyrimidine rings make a dihedral angle of 5.285 (6)°. Inter­molecular O—H⋯O hydrogen bonds link the six water mol­ecules, generating edge-fused four-, five- or six-membered ring motifs and forming two-dimensional sheets. The sheets are stabilized by the formation of O—H⋯N hydrogen bonds between the water mol­ecules and the bipyrimidine mol­ecules, resulting in a three-dimensional network. International Union of Crystallography 2009-03-25 /pmc/articles/PMC2968866/ /pubmed/21582567 http://dx.doi.org/10.1107/S1600536809010095 Text en © Ma 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
Ma, Yanni
Zhou, Le
Deng, Dongsheng
Ji, Baoming
4,4′,6,6′-Tetra­methyl-2,2′-bipyrimidine hexa­hydrate
title 4,4′,6,6′-Tetra­methyl-2,2′-bipyrimidine hexa­hydrate
title_full 4,4′,6,6′-Tetra­methyl-2,2′-bipyrimidine hexa­hydrate
title_fullStr 4,4′,6,6′-Tetra­methyl-2,2′-bipyrimidine hexa­hydrate
title_full_unstemmed 4,4′,6,6′-Tetra­methyl-2,2′-bipyrimidine hexa­hydrate
title_short 4,4′,6,6′-Tetra­methyl-2,2′-bipyrimidine hexa­hydrate
title_sort 4,4′,6,6′-tetra­methyl-2,2′-bipyrimidine hexa­hydrate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968866/
https://www.ncbi.nlm.nih.gov/pubmed/21582567
http://dx.doi.org/10.1107/S1600536809010095
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AT zhoule 4466tetramethyl22bipyrimidinehexahydrate
AT dengdongsheng 4466tetramethyl22bipyrimidinehexahydrate
AT jibaoming 4466tetramethyl22bipyrimidinehexahydrate

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