We report the synthesis and structural diversity of Zn(II) metal-organic framework (MOF) with in situ formation of tetrazole ligand 3-ptz [3-ptz = 5-(3-pyridyl)tetrazolate] as a function pH. By varying the initial reaction pH, we obtain high-quality crystals of the noncentrosymmetric three-dimensional MOF Zn(3-ptz)₂, mixed phases involving the zinc-aqua complex [Zn(H₂O)₄(3-ptz)₂]·4H₂O, and two-dimensional MOF crystals Zn(OH)(3-ptz) with a tunable microrod morphology, keeping reaction time, temperature, and metal–ligand molar ratio constant. Structures are characterized by X-ray diffraction, scanning electron microscopy, Fourier transform infrared spectroscopy, and UV–vis spectroscopy. We discuss the observed structural diversity in terms of the relative abundance of hydroxo-zinc species in solution for different values of pH.

Mixed-valence polyoxovanadates (POVs) constitute a family of polyoxometalates whose electronic properties are still unclear. Polyoxovanadoborates (POVBs), a subfamily of POVs, show different electronic and magnetic properties compared to those of POVs. Upon the interpretation of the electronic spectra of these compounds, only three bands in the 350–800 nm range were reported in the literature. This is the first theoretical study of the electronic spectra of the [V₁₂B₁₈O₆₀] family, and we showed that these three bands are the contributions of different excitations, i.e., LMCT + IVCT, d–d + IVCT and d–d + IVCT. We showed experimentally that in the NIR region, up to 1800 nm, IVCT transitions appear, whose intensity is dependent on the mixed-valence ratio. We also showed that the condensation of borate groups resulted in the loss of the differentiation of the vanadyl stretching vibration that depends on the oxidation state, which is as expected for other types of polyoxovanadates. This feature was proposed as a probe to observe the delocalized to localized phase transition in POVs.