Tris(1,2-diaminoethane)nickel(II) hexafluoridosilicate
The ionic title complex, [Ni(C2H8N2)3](SiF6), is built up of [Ni(en)3]2+ complex cations (en = 1,2-diaminoethane) and hexafluoridosilicate anions. Single crystals of the title complex were isolated from an aqueous–ethanolic Ni2+–en–SiF62− syste...
Main Authors: | , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
International Union of Crystallography
2010-11-01
|
Series: | Acta Crystallographica Section E |
Online Access: | http://scripts.iucr.org/cgi-bin/paper?S1600536810041553 |
id |
doaj-e98202605abd46b5b327de2797383f5b |
---|---|
record_format |
Article |
spelling |
doaj-e98202605abd46b5b327de2797383f5b2020-11-25T01:38:20ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682010-11-016611m1451m145210.1107/S1600536810041553Tris(1,2-diaminoethane)nickel(II) hexafluoridosilicateJaroslava HaníkováJuraj KuchárJuraj ČernákGiorgio PelosiThe ionic title complex, [Ni(C2H8N2)3](SiF6), is built up of [Ni(en)3]2+ complex cations (en = 1,2-diaminoethane) and hexafluoridosilicate anions. Single crystals of the title complex were isolated from an aqueous–ethanolic Ni2+–en–SiF62− system. The Ni(II) and Si atoms are each located on a special position with site symmetry 3.2. The Ni(II) atom coordination sphere is octahedrally deformed, being coordinated by three chelating diamine ligands with an Ni—N distance of 2.1233 (18) Å. The crystal packing of the respective ions corresponds to the structure type of the hexagonal form of BN. Beside ionic forces, the packing is governed by N—H...F hydrogen bonds, which lead to the formation of hydrophobic channels running along the 63 screw axis. The structure was refined as an inversion twin [0.49 (3): 0.51 (3)]. http://scripts.iucr.org/cgi-bin/paper?S1600536810041553 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jaroslava Haníková Juraj Kuchár Juraj Černák Giorgio Pelosi |
spellingShingle |
Jaroslava Haníková Juraj Kuchár Juraj Černák Giorgio Pelosi Tris(1,2-diaminoethane)nickel(II) hexafluoridosilicate Acta Crystallographica Section E |
author_facet |
Jaroslava Haníková Juraj Kuchár Juraj Černák Giorgio Pelosi |
author_sort |
Jaroslava Haníková |
title |
Tris(1,2-diaminoethane)nickel(II) hexafluoridosilicate |
title_short |
Tris(1,2-diaminoethane)nickel(II) hexafluoridosilicate |
title_full |
Tris(1,2-diaminoethane)nickel(II) hexafluoridosilicate |
title_fullStr |
Tris(1,2-diaminoethane)nickel(II) hexafluoridosilicate |
title_full_unstemmed |
Tris(1,2-diaminoethane)nickel(II) hexafluoridosilicate |
title_sort |
tris(1,2-diaminoethane)nickel(ii) hexafluoridosilicate |
publisher |
International Union of Crystallography |
series |
Acta Crystallographica Section E |
issn |
1600-5368 |
publishDate |
2010-11-01 |
description |
The ionic title complex, [Ni(C2H8N2)3](SiF6), is built up of [Ni(en)3]2+ complex cations (en = 1,2-diaminoethane) and hexafluoridosilicate anions. Single crystals of the title complex were isolated from an aqueous–ethanolic Ni2+–en–SiF62− system. The Ni(II) and Si atoms are each located on a special position with site symmetry 3.2. The Ni(II) atom coordination sphere is octahedrally deformed, being coordinated by three chelating diamine ligands with an Ni—N distance of 2.1233 (18) Å. The crystal packing of the respective ions corresponds to the structure type of the hexagonal form of BN. Beside ionic forces, the packing is governed by N—H...F hydrogen bonds, which lead to the formation of hydrophobic channels running along the 63 screw axis. The structure was refined as an inversion twin [0.49 (3): 0.51 (3)]. |
url |
http://scripts.iucr.org/cgi-bin/paper?S1600536810041553 |
work_keys_str_mv |
AT jaroslavahanamp237kovamp225 tris12diaminoethanenickeliihexafluoridosilicate AT jurajkuchamp225r tris12diaminoethanenickeliihexafluoridosilicate AT jurajamp268ernamp225k tris12diaminoethanenickeliihexafluoridosilicate AT giorgiopelosi tris12diaminoethanenickeliihexafluoridosilicate |
_version_ |
1725054439922860032 |