文摘
The organic–inorganic hybrid compound 1,4-butyldiammonium hexaaquadicadmium(II) trisulfate (Cb>4b>Hb>14b>Nb>2b>)[Cdb>2b>(Hb>2b>O)b>6b>(SOb>4b>)b>3b>] (<b>1b>) was synthesized by the reaction of 3CdSOb>4b><b>·b>8Hb>2b>O with 1,4-butanediamine in sulfuric acid aqueous solution. Differential scanning calorimetry measurements indicate that <b>1b> undergoes a reversible phase transition at 243.4 K with a thermal hysteresis of 3.3 K. Single-crystal X-ray diffraction data disclose that the phase transition is from the room-temperature phase with the space group C2/c to the low-temperature phase with the space group P1 with the Aizu notation of 2/mF1. The structural phase transition of <b>1b> is ascribed to the coupling of disorder–order transformations of the flexible 1,4-butyldiammonium cation and a sulfate anion and reorientation of the cation. The temperature dependence of the dielectric permittivity demonstrates a step-like change in the range 200–260 K, which makes (Cb>4b>Hb>14b>Nb>2b>)[Cdb>2b>(Hb>2b>O)b>6b>(SOb>4b>)b>3b>] a promising switchable dielectric material. The results could offer an avenue to design switchable dielectric materials through the synergistic effect of disorder–order transitions and reorientation motion.