Abstract: | The title coordination polymer, {Cd2(CH2N5)(C6H4NO2)Cl(OH)]·0.14H2O}n, (I), was synthesized by the reaction of cadmium acetate and N‐(1H‐tetrazol‐5‐yl)isonicotinamide in aqueous ammonia, using hydrochloric acid to adjust the pH. Under hydrothermal conditions, N‐(1H‐tetrazol‐5‐yl)isonicotinamide slowly hydrolyzes to form isonicotinic acid (Hisonic) and 5‐aminotetrazole (Hatz). The deprotonated form of isonicotinic acid (denoted isonic) acts as a bridging ligand in the structure. The polymer crystallizes in the monoclinic space group C2/m. In the structure, there is one Cd3(μ3‐OH) unit of Cs symmetry, with one of the CdII atoms and the O and H atoms located on a mirror plane. The other crystallographically independent CdII cation is located on an inversion centre. Each edge of the Cd3(μ3‐OH) isosceles triangle is bridged by an atz ligand in a μ1,2 or μ2,3/μ3,4 mode. The Cd3(μ3‐OH) units are laced around with a belt of chloride ligands. The belts are further connected into undulating layers via weak inter‐belt Cd—Cl bonds. The two organic ligands reside across mirror planes. The construction of a three‐dimensional framework is completed by the pillaring isonic ligand. Water molecules partially occupy the voids of the framework. |