![[HTML version]](/e/graphics/htmlborder.gif)
![[PDF version]](/e/graphics/pdfborder.gif)
![[CIF]](/e/graphics/cifborder.gif)
![[3d view]](/e/graphics/3dviewborder.gif)
![[Structure Factors]](/e/graphics/structurefactorsborder.gif)
![[Supplementary Material]](/e/graphics/supplementarymaterialsborder.gif)
![[CIF check Report]](/e/graphics/checkcifborder.gif)
![[Open access]](/e/graphics/free.gif)
![[Contents scheme]](cv2460contents.gif)
Acta Cryst. (2008). E64, o2100 [ doi:10.1107/S1600536808032340 ]
Abstract: The title compound, C8H20N+·Cl-·H2O, has been prepared by a simple one-pot synthesis route followed by anion exchange using resin. In the crystal structure, the cations are packed in such a way that channels exist parallel to the b axis. These channels are filled by the anions and water molecules, which interact via O-H
Cl hydrogen bonds [O
Cl = 3.285 (3) and 3.239 (3) Å] to form helical chains. The cations are involved in weak intermolecular C-H
Cl and C-H
O hydrogen bonds. The title compound is not isomorphous with the bromo or iodo analogues.
Online 11 October 2008
Copyright © International Union of Crystallography
IUCr Webmaster