One of the simplest routes to prepare polycrystalline Zn(OH) 2 is by coprecipitation, with zinc nitrate as a cation source. However, the addition of even minute amounts of manganese nitrate to the precursors used to prepare pure Zn(OH) 2 results in Mn 2+ doped nanostructured ZnO. The comparison with other Mn 2+ doped metal hydroxides prepared by the same coprecipitation method, involving metal nitrates precursors, shows that this behavior is unique, pertaining only to Zn(OH) 2 . A systematic study of the samples prepared without and with variable amounts of Mn 2+ ions, in the 1 to 5000 ppm nominal concentrations range showed that the re-routing of the reaction takes place even for the lowest nominal dopant concentration of 1 ppm. According to X-ray diffraction, transmission electron microscopy and Fourier transform infrared spectroscopy investigations, both crystallite size and morphology of the resulting nanostructured ZnO samples varied with the Mn 2+ nominal concentration. Moreover, quantitative electron paramagnetic resonance investigations showed that the incorporation rate of the Mn 2+ ions at different sites in the nanostructured ZnO depended on the nominal Mn 2+ concentration. The results are discussed in terms of the coordination properties of the Mn 2+ and Zn 2+ ions and the nature of the reaction precursors.Fig. 2 TEM/HRTEM images and the corresponding ED patterns (insets) for the ZnO samples doped with 1 ppm (a), 1000 ppm (b), 5000 ppm (c) Mn 2+ nominal concentration. (d) HRTEM image at larger magnification of the sample with Mn 2+ 5000 ppm nominal concentration. The ED patterns were indexed with the ZnO structure. 106734 | RSC Adv., 2016, 6, 106732-106741 This journal isFig. 3 Multiscan Q-band EPR spectra for the undoped (bottom) and Mn 2+ doped (upper) samples. The six hyperfine lines/doublet-lines of the Mn 2+ (a), Mn 2+ (d)/Mn 2+ (c) paramagnetic centers are marked with vertical bars.This journal is