Abstract
Abstract Two polytopic azoles, 1,4-bis(pyrazol-4-yl)benzene and 1,4-bis(tetrazol-5-yl)benzene, were prepared in sizable amounts by high yield syntheses employing, in mild conditions, cheap reactants and, whenever possible, aqueous solutions. The two species were characterized by 1H and 13C NMR spectroscopy and by thermal analyses, the latter evidencing their high chemical and thermal stability. X-ray powder diffraction methods disclosed their non isomorphous crystal structures, in which individual molecules interact via hydrogen bonds to form two-dimensional sheets.
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