Mączka Mirosław, Pietraszko Adam, Macalik Bogusław, Hermanowicz Krzysztof
Institute of Low Temperature and Structure Research , Polish Academy of Sciences, P.O. Box 1410, 50-950 Wrocław 2, Poland.
Inorg Chem. 2014 Jan 21;53(2):787-94. doi: 10.1021/ic4020702. Epub 2014 Jan 3.
We report the synthesis, crystal structure, thermal, dielectric, IR, and Raman studies of [NH4][Mg(HCOO)3] formate. Single-crystal X-ray diffraction shows that it crystallizes in the hexagonal space group P6322, with orientationally disordered NH4(+) ions located in the cages of the network. Upon cooling, [NH4][Mg(HCOO)3] undergoes a phase transition at around 255 K to the ferroelectric P63 structure. Raman and IR spectra show a strong increase in intensity of the N-H stretching bands as well as narrowing of the bands related to the NH4(+) ions upon cooling. These changes indicate that the phase transition is due to orientational ordering of the NH4(+) ions. Analysis of the Raman data show, however, that the rotational and translational motions of NH4(+) do not freeze completely at the phase transition but exhibit further slowing down below 255 K, and the motional freezing becomes nearly complete below 140 K.
我们报道了甲酸铵[NH₄][Mg(HCOO)₃]的合成、晶体结构、热学、介电、红外和拉曼研究。单晶X射线衍射表明它结晶于六方空间群P6322,其中取向无序的NH₄⁺离子位于网络的笼中。冷却时,[NH₄][Mg(HCOO)₃]在约255 K时经历相变成为铁电P63结构。拉曼光谱和红外光谱显示,冷却时N - H伸缩带的强度大幅增加,与NH₄⁺离子相关的谱带变窄。这些变化表明相变是由于NH₄⁺离子的取向有序化。然而,对拉曼数据的分析表明,NH₄⁺的旋转和平移运动在相变时并未完全冻结,而是在255 K以下进一步减慢,在140 K以下运动冻结几乎完全。