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Diaquabis­[3-(hydroxy­imino)­butanoato]nickel(II)

In the neutral, mononuclear title complex, [Ni(C(4)H(6)NO(3))(2)(H(2)O)(2)], the Ni atom lies on a crystallographic inversion centre within a distorted octa­hedral N(2)O(4) environment. Two trans-disposed anions of 3-hydroxy­imino­butanoic acid occupy four equatorial sites, coordinated by the deprot...

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Autores principales: Dudarenko, Nikolay M., Kalibabchuk, Valentina A., Malysheva, Maria L., Iskenderov, Turganbay S., Gumienna-Kontecka, Elżbieta
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983569/
https://www.ncbi.nlm.nih.gov/pubmed/21580224
http://dx.doi.org/10.1107/S1600536810004605
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author Dudarenko, Nikolay M.
Kalibabchuk, Valentina A.
Malysheva, Maria L.
Iskenderov, Turganbay S.
Gumienna-Kontecka, Elżbieta
author_facet Dudarenko, Nikolay M.
Kalibabchuk, Valentina A.
Malysheva, Maria L.
Iskenderov, Turganbay S.
Gumienna-Kontecka, Elżbieta
author_sort Dudarenko, Nikolay M.
collection PubMed
description In the neutral, mononuclear title complex, [Ni(C(4)H(6)NO(3))(2)(H(2)O)(2)], the Ni atom lies on a crystallographic inversion centre within a distorted octa­hedral N(2)O(4) environment. Two trans-disposed anions of 3-hydroxy­imino­butanoic acid occupy four equatorial sites, coordinated by the deprotonated carboxyl­ate and protonated oxime groups and forming six-membered chelate rings, while the two axial positions are occupied by the water O atoms. The O atom of the oxime group forms an intra­molecular hydrogen bond with the coordinated carboxyl­ate O atom. The complex mol­ecules are linked into chains along b by hydrogen bonds between the water O atom and the carboxyl­ate O of a neighbouring mol­ecule. The chains are linked by further hydrogen bonds into a layer structure.
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spelling pubmed-29835692010-12-30 Diaquabis­[3-(hydroxy­imino)­butanoato]nickel(II) Dudarenko, Nikolay M. Kalibabchuk, Valentina A. Malysheva, Maria L. Iskenderov, Turganbay S. Gumienna-Kontecka, Elżbieta Acta Crystallogr Sect E Struct Rep Online Metal-Organic Papers In the neutral, mononuclear title complex, [Ni(C(4)H(6)NO(3))(2)(H(2)O)(2)], the Ni atom lies on a crystallographic inversion centre within a distorted octa­hedral N(2)O(4) environment. Two trans-disposed anions of 3-hydroxy­imino­butanoic acid occupy four equatorial sites, coordinated by the deprotonated carboxyl­ate and protonated oxime groups and forming six-membered chelate rings, while the two axial positions are occupied by the water O atoms. The O atom of the oxime group forms an intra­molecular hydrogen bond with the coordinated carboxyl­ate O atom. The complex mol­ecules are linked into chains along b by hydrogen bonds between the water O atom and the carboxyl­ate O of a neighbouring mol­ecule. The chains are linked by further hydrogen bonds into a layer structure. International Union of Crystallography 2010-02-10 /pmc/articles/PMC2983569/ /pubmed/21580224 http://dx.doi.org/10.1107/S1600536810004605 Text en © Dudarenko et al. 2010 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
Dudarenko, Nikolay M.
Kalibabchuk, Valentina A.
Malysheva, Maria L.
Iskenderov, Turganbay S.
Gumienna-Kontecka, Elżbieta
Diaquabis­[3-(hydroxy­imino)­butanoato]nickel(II)
title Diaquabis­[3-(hydroxy­imino)­butanoato]nickel(II)
title_full Diaquabis­[3-(hydroxy­imino)­butanoato]nickel(II)
title_fullStr Diaquabis­[3-(hydroxy­imino)­butanoato]nickel(II)
title_full_unstemmed Diaquabis­[3-(hydroxy­imino)­butanoato]nickel(II)
title_short Diaquabis­[3-(hydroxy­imino)­butanoato]nickel(II)
title_sort diaquabis­[3-(hydroxy­imino)­butanoato]nickel(ii)
topic Metal-Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983569/
https://www.ncbi.nlm.nih.gov/pubmed/21580224
http://dx.doi.org/10.1107/S1600536810004605
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