首页> 外文期刊>International Journal of Quantum Chemistry >Synthesis of chloroantimonates(III) with selected organic cations. X-ray studies of phase transition in ferroelectric tris(trimethylammonium) nonachlorodiantimonate(III) at 125 K
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Synthesis of chloroantimonates(III) with selected organic cations. X-ray studies of phase transition in ferroelectric tris(trimethylammonium) nonachlorodiantimonate(III) at 125 K

机译:具有选定有机阳离子的氯锑酸酯(III)的合成。铁电三(三甲基铵)壬二氯二锑酸盐(III)在125 K时的相变的X射线研究

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The dependence of molar ratio of reactants on the formula, crystal structure and physicochemical properties of chloroantimonates(III) with different organic cations was studied. It was proved, that the compounds show preferences in crystallization of one product. The changes of the molar ratio of substrates lead to the corresponding changes of these components in crystallized products. The structure of ferroelectric chloroantimonate(III), [(CH3)(3)NH](3)[SbCl9], was determined at 165 and 95 K. It crystallizes in monoclinic space group Pc: a = 9.9612(11), b = 9.0714(8), c = 15.1807(14) Angstrom, beta = 90.086(8)degrees, R-1 = 0.0202, wR(2) = 0.0405 and a = 9.9138(10), b = 9.0783(7), c = 15.1299(14)Angstrom, beta = 90.026(8)degrees, R-1 = 0.0163, wR(2) = 0.0356 at 165 and 95 K respectively. At both temperatures the crystal is built of polyanionic layers and trimethylammonium cations. They are bound together by the system of hydrogen bonds. The molecular motions of the organic cations are gradually frozen with decreasing temperature. At 165 K all cations are ordered. The non-structural ferro-ferroelectric phase transition at 125 K is associated with changes in the dynamics of trimethylammonium cations. (C) 2004 Elsevier Inc. All rights reserved.
机译:研究了反应物摩尔比对不同有机阳离子型氯锑酸盐(III)分子式,晶体结构和理化性质的影响。已经证明,该化合物在一种产物的结晶中显示出偏爱。底物摩尔比的变化导致结晶产物中这些组分的相应变化。在165和95 K下确定了铁电氯锑酸(III)[[CH3](3)NH](3)[SbCl9]的结构。它在单斜空间群Pc中结晶:a = 9.9612(11),b = 9.0714(8),c = 15.1807(14)埃,beta = 90.086(8)度,R-1 = 0.0202,wR(2)= 0.0405和a = 9.9138(10),b = 9.0783(7),c = 15.1299(14)埃,β= 90.026(8)度,R-1 = 0.0163,wR(2)= 0.0356在165和95 K时。在两个温度下,晶体都是由聚阴离子层和三甲基铵阳离子构成的。它们通过氢键系统结合在一起。随着温度的降低,有机阳离子的分子运动逐渐冻结。在165 K时订购所有阳离子。 125 K时的非结构性铁电相变与三甲基铵阳离子动力学的变化有关。 (C)2004 Elsevier Inc.保留所有权利。

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