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Lithium diaquanickel(II) catena-borodiphosphate(V) monohydrate
The title borophosphate LiNi(H(2)O)(2)[BP(2)O(8)]·H(2)O was synthesized under hydrothermal conditions. The crystal structure is isotypic with the Mg analogue and features helical [BP(2)O(8)](3−) borophosphate ribbons, constructed by BO(4) (2 symmetry) and PO(4) tetrahedra. The borate groups share...
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969569/ https://www.ncbi.nlm.nih.gov/pubmed/21582977 http://dx.doi.org/10.1107/S1600536809014652 |
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author | Zheng, Juan Zhang, Aiyun |
author_facet | Zheng, Juan Zhang, Aiyun |
author_sort | Zheng, Juan |
collection | PubMed |
description | The title borophosphate LiNi(H(2)O)(2)[BP(2)O(8)]·H(2)O was synthesized under hydrothermal conditions. The crystal structure is isotypic with the Mg analogue and features helical [BP(2)O(8)](3−) borophosphate ribbons, constructed by BO(4) (2 symmetry) and PO(4) tetrahedra. The borate groups share all their oxygen apices with adjacent phosphate tetrahedra. The ribbons are connected via Ni(2+) cations that are located on twofold rotation axes. The cations have a slightly distorted octahedral oxygen coordination by four O atoms from the anion and by two water molecules. The voids within the helices are occupied by Li(+) cations, likewise located on twofold rotation axes, in an irregular environment of five O atoms. The structure is stabilized by O—H⋯O hydrogen bonds between coordinated or uncoordinated water molecules and O atoms that are part of the helices. |
format | Text |
id | pubmed-2969569 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29695692010-12-30 Lithium diaquanickel(II) catena-borodiphosphate(V) monohydrate Zheng, Juan Zhang, Aiyun Acta Crystallogr Sect E Struct Rep Online Inorganic Papers The title borophosphate LiNi(H(2)O)(2)[BP(2)O(8)]·H(2)O was synthesized under hydrothermal conditions. The crystal structure is isotypic with the Mg analogue and features helical [BP(2)O(8)](3−) borophosphate ribbons, constructed by BO(4) (2 symmetry) and PO(4) tetrahedra. The borate groups share all their oxygen apices with adjacent phosphate tetrahedra. The ribbons are connected via Ni(2+) cations that are located on twofold rotation axes. The cations have a slightly distorted octahedral oxygen coordination by four O atoms from the anion and by two water molecules. The voids within the helices are occupied by Li(+) cations, likewise located on twofold rotation axes, in an irregular environment of five O atoms. The structure is stabilized by O—H⋯O hydrogen bonds between coordinated or uncoordinated water molecules and O atoms that are part of the helices. International Union of Crystallography 2009-05-07 /pmc/articles/PMC2969569/ /pubmed/21582977 http://dx.doi.org/10.1107/S1600536809014652 Text en © Zheng and Zhang 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 | Inorganic Papers Zheng, Juan Zhang, Aiyun Lithium diaquanickel(II) catena-borodiphosphate(V) monohydrate |
title | Lithium diaquanickel(II) catena-borodiphosphate(V) monohydrate |
title_full | Lithium diaquanickel(II) catena-borodiphosphate(V) monohydrate |
title_fullStr | Lithium diaquanickel(II) catena-borodiphosphate(V) monohydrate |
title_full_unstemmed | Lithium diaquanickel(II) catena-borodiphosphate(V) monohydrate |
title_short | Lithium diaquanickel(II) catena-borodiphosphate(V) monohydrate |
title_sort | lithium diaquanickel(ii) catena-borodiphosphate(v) monohydrate |
topic | Inorganic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969569/ https://www.ncbi.nlm.nih.gov/pubmed/21582977 http://dx.doi.org/10.1107/S1600536809014652 |
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