Abstract
Self-assembly of flexible [3-(2-pyridyl)-1-pyrazolyl] acetic acid (Hpypza) with ZnCl2·4H2O, CdCl2·4H2O, and Mn(OAc)2·4H2O affords three new coordination polymers [M(pypza)(HCOO)]n (M = Zn for 1; Cd for 2) and [Mn(pypza)(OAc)]n (3), which are significantly different from the previously reported complexes [Zn(pypza)Cl]2, [Cd(pypza)Cl]n, [Mn(pypza)Cl]2, and [Mn(pypza)Cl]n. These structural differences may be ascribed to the use of different solvents and anions. Single-crystal X-ray diffraction analyses of these polymers indicate that 1 and 2 are isostructural with a 2-D coordination network via bridging pypza− and HCOO− resulting from the hydrolysis of DMF, and 3 also displays a 2-D network connected via pypza− and OAc−. These complexes have been characterized by IR, microanalysis, and powder X-ray diffraction techniques. In addition, the solid fluorescence and thermal stability properties of 1–3 have also been investigated. Magnetic properties of the MnII complex have also been measured.
Graphical Abstract
Self-assembly of flexible [3-(2-pyridyl)-1-pyrazolyl] acetic acid (Hpypza) with ZnCl2·4H2O, CdCl2·4H2O, and Mn(OAc)2·4H2O affords three new coordination polymers [M(pypza)(HCOO)]n (M = Zn for 1; Cd for 2) and [Mn(pypza)(OAc)]n (3), which are significantly different from the previously reported complexes [Zn(pypza)Cl]2, [Cd(pypza)Cl]n, [Mn(pypza)Cl]2, and [Mn(pypza)Cl]n. These structural differences may be ascribed to the use of different solvents and anions.