![[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]](zl2142contents.gif)
Acta Cryst. (2008). E64, o2058 [ doi:10.1107/S1600536808031322 ]
Abstract: Crystals of the title adduct, C10H8N2·2C3H3NO2, were obtained from a methanol/water solution of cyanoacetic acid and 4,4'-bipyridine at room temperature. In the crystal structure, cyanoacetic acid and centrosymmetric 4,4'-bipyridine molecules are linked by O-H
N hydrogen bonds to form three-component supramolecular adducts. The acidic H atom is almost midway between the O and N atoms of the cyanoacetic acid and bipyridine molecules, with O-H and N-H distances of 1.19 (3) and 1.39 (3) Å, respectively, so that the H-atom transfer is best regarded as partial. The three-component adducts are further interconnected with neighboring molecules by weak intermolecular C-H
O and C-H
N hydrogen bonds and by
-
stacking interactions [centroid-centroid distance = 3.7200 (11) Å] to generate a three-dimensional supramolecular structure.
Online 4 October 2008
Copyright © International Union of Crystallography
IUCr Webmaster