Glycine zinc sulfate penta-hydrate: redetermination at 10 K from time-of-flight neutron Laue diffraction.

Single crystals of glycine zinc sulfate penta-hydrate [systematic name: hexa-aqua-zinc tetra-aquadiglycinezinc bis-(sulfate)], [Zn(HO)][Zn(CHNO)(HO)](SO), have been grown by isothermal evaporation from aqueous solution at room temperature and characterized by single-crystal neutron diffraction. The unit cell contains two unique ZnO octa-hedra on sites of symmetry -1 and two SO tetra-hedra with site symmetry 1; the octa-hedra comprise one [tetra-aqua-diglycine zinc] ion (centred on one Zn atom) and one [hexa-aqua-zinc] ion (centred on the other Zn atom); the glycine zwitterion, NHCHCOO, adopts a monodentate coordination to the first Zn atom. All other atoms sit on general positions of site symmetry 1. Glycine forms centrosymmetric closed cyclic dimers due to N-H⋯O hydrogen bonds between the amine and carboxyl-ate groups of adjacent zwitterions and exhibits torsion angles varying from ideal planarity by no more than 1.2°, the smallest values for any known glycine zwitterion not otherwise constrained by a mirror plane. This work confirms the H-atom locations estimated in three earlier single-crystal X-ray diffraction studies with the addition of independently refined fractional coordinates and parameters, which provide accurate inter-nuclear -H ( = N, O) bond lengths and consequently a more accurate and precise depiction of the hydrogen-bond framework.