Subject: morality milk

From: "Matthew Kline" <[email-masked]>
Date: Tue, 26 Sep 2006 13:38:05 -0600

The bond lengths within the system indicate some degree of delocalization. N interactions connect these chains into a two-dimensional layer.
O hydrogen bonds, resulting in inversion-symmetry generated dimers. These dimers are located around centres of inversion.
Both intra- and intermolecular hydrogen bonds are present between the hydroxyl groups, resulting in a one-dimensional hydrogen-bonding network.
N hydrogen bond, which stabilizes the configuration.
O hydrogen bonds link the molecules into zigzag chains along the b axis.
N hydrogen-bond interactions are present, resulting in a one-dimensional supramolecular chain structure.
The ethoxybenzene and chlorophenyl rings are located on the same side of the heterocyclic system, resembling the two front claws of a crab.
Each conformer resides on a centre of inversion.
Cl hydrogen bonds link cations and anions to form one-dimensional ladders propagating in the a-axis direction. O hydrogen bonds, forming a chain. All bond lengths and angles show normal values.
O hydrogen bonds link the molecules into dimers, which may be effective in the stabilization of the crystal structure. O hydrogen bonds, resulting in inversion-symmetry generated dimers.
N hydrogen bonds into linear chains.
N hydrogen bond with an O. The crystal structure contains three very weak intermolecular hydrogen bonds, viz. O hydrogen bonds link the molecules into dimers, which may be effective in the stabilization of the crystal structure. O hydrogen bonds, forming centrosymmetric dimers. O hydrogen bonds involving a sulfone O atom and an aromatic CH group, forming centrosymmetric dimers.
O hydrogen bonds stabilize the structure. There are two molecules in the asymmetric unit which differ in conformation.
Geometric parameters are in normal ranges. The bond lengths within the system indicate some degree of delocalization. The molecule is approximately planar for all non-H atoms.
O hydrogen bonds, forming a three-dimensional hydrogen-bond network.
The ethoxybenzene and chlorophenyl rings are located on the same side of the heterocyclic system, resembling the two front claws of a crab. An intramolecular hydrogen bond occurs between the oxazole and hydroxy groups. All bond lengths and angles show normal values. N hydrogen-bond interactions are present, resulting in a one-dimensional supramolecular chain structure.