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Disodium diaqua­bis­(methyl­enedi­phos­pho­nato-κ(2) O,O′)cobaltate(II) dihydrate

In the title compound, Na(2)[Co(CH(4)O(6)P(2))(2)(H(2)O)(2)]·2H(2)O, the asymmetric unit is composed of one methyl­enediphospho­nate ligand and one water mol­ecule, which both are coordinated to a Co(II) atom, as well as a non-coordinated water mol­ecule and a sodium cation. The Co(II) atom occupies...

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Autores principales: van Merwe, Kina, Visser, Hendrik G., Venter, Johan A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3201543/
https://www.ncbi.nlm.nih.gov/pubmed/22058722
http://dx.doi.org/10.1107/S1600536811038530
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author van Merwe, Kina
Visser, Hendrik G.
Venter, Johan A.
author_facet van Merwe, Kina
Visser, Hendrik G.
Venter, Johan A.
author_sort van Merwe, Kina
collection PubMed
description In the title compound, Na(2)[Co(CH(4)O(6)P(2))(2)(H(2)O)(2)]·2H(2)O, the asymmetric unit is composed of one methyl­enediphospho­nate ligand and one water mol­ecule, which both are coordinated to a Co(II) atom, as well as a non-coordinated water mol­ecule and a sodium cation. The Co(II) atom occupies a special position on a crystallographic inversion centre. The slightly distorted Co(II)O(6) octa­hedral coordination environment is composed of two bidentate methyl­enediphospho­nate ligands and two coordinated water mol­ecules in trans positions. The sodium ion is octa­hedrally coordinated to six O atoms with Na—O distances ranging from 2.3149 (12) to 2.6243 (12) Å. An extensive three-dimensional network of inter­molecular as well as intra­molecular O—H⋯O and C—H⋯O hydrogen bonding inter­acions is present.
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spelling pubmed-32015432011-11-06 Disodium diaqua­bis­(methyl­enedi­phos­pho­nato-κ(2) O,O′)cobaltate(II) dihydrate van Merwe, Kina Visser, Hendrik G. Venter, Johan A. Acta Crystallogr Sect E Struct Rep Online Metal-Organic Papers In the title compound, Na(2)[Co(CH(4)O(6)P(2))(2)(H(2)O)(2)]·2H(2)O, the asymmetric unit is composed of one methyl­enediphospho­nate ligand and one water mol­ecule, which both are coordinated to a Co(II) atom, as well as a non-coordinated water mol­ecule and a sodium cation. The Co(II) atom occupies a special position on a crystallographic inversion centre. The slightly distorted Co(II)O(6) octa­hedral coordination environment is composed of two bidentate methyl­enediphospho­nate ligands and two coordinated water mol­ecules in trans positions. The sodium ion is octa­hedrally coordinated to six O atoms with Na—O distances ranging from 2.3149 (12) to 2.6243 (12) Å. An extensive three-dimensional network of inter­molecular as well as intra­molecular O—H⋯O and C—H⋯O hydrogen bonding inter­acions is present. International Union of Crystallography 2011-09-30 /pmc/articles/PMC3201543/ /pubmed/22058722 http://dx.doi.org/10.1107/S1600536811038530 Text en © Merwe et al. 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 Metal-Organic Papers
van Merwe, Kina
Visser, Hendrik G.
Venter, Johan A.
Disodium diaqua­bis­(methyl­enedi­phos­pho­nato-κ(2) O,O′)cobaltate(II) dihydrate
title Disodium diaqua­bis­(methyl­enedi­phos­pho­nato-κ(2) O,O′)cobaltate(II) dihydrate
title_full Disodium diaqua­bis­(methyl­enedi­phos­pho­nato-κ(2) O,O′)cobaltate(II) dihydrate
title_fullStr Disodium diaqua­bis­(methyl­enedi­phos­pho­nato-κ(2) O,O′)cobaltate(II) dihydrate
title_full_unstemmed Disodium diaqua­bis­(methyl­enedi­phos­pho­nato-κ(2) O,O′)cobaltate(II) dihydrate
title_short Disodium diaqua­bis­(methyl­enedi­phos­pho­nato-κ(2) O,O′)cobaltate(II) dihydrate
title_sort disodium diaqua­bis­(methyl­enedi­phos­pho­nato-κ(2) o,o′)cobaltate(ii) dihydrate
topic Metal-Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3201543/
https://www.ncbi.nlm.nih.gov/pubmed/22058722
http://dx.doi.org/10.1107/S1600536811038530
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