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Structural, magnetic, and spectroscopic studies of YAgSn, TmAgSn, and LuAgSn

机译:YAgSn,TmAgSn和LuAgSn的结构,磁学和光谱学研究

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The rare earth-silver-stannides YAgSn, TmAgSn, and LuAgSn were synthesized from the elements by arc-melting and subsequent annealing. The three stannides were investigated by X-ray powder and single-crystal diffraction: NdPtSb type, P6(3)MC, Z = 2, a = 468.3(1), c = 737.2(2)pm, wR(2) = 0.0343, 353 F-2 values, 12 variables for YAgSn, and ZrNiAl type, P (6) over bar 2m, a = 726.4(2), c = 443.7(1) pm, wR(2) = 0.0399, 659 F-2 values, 15 variables for TmAgSn, and a = 723.8(2), c = 442.47(9) pm, wR(2) = 0.0674, 364 F-2 values, 15 variables for LuAgSn. Besides conventional laboratory X-ray data with monochromatized Mo radiation, the structures were also refined on the basis of synchrotron data with lambda = 48.725 pm, in order to clarify the silver-tin ordering more precisely. YAgSn has puckered, two-dimensional [AgSn] networks with Ag-Sn distances of 278 pm, while the [AgSn] networks of TmAgSn and LuAgSn are three-dimensional with Ag-Sn distances of 279 and 284 pm for LuAgSn. Susceptibility measurements indicate Pauli paramagnetism for YAgSn and LuAgSn. TmAgSn is a Curie-Weiss paramagnet with an experimental magnetic moment of 7.2 mu(B)/Tm. No magnetic ordering is evident down to 2K. The local environments of the tin sites in these compounds were characterized by Sn-119 Mossbauer spectroscopy and solid-state NMR (in YAgSn and LuAgSn), confirming the tin site multiplicities proposed from the structure solutions and the absence of Sn/Ag site disordering. Mossbauer quadrupolar splittings were found in good agreement with calculated electric field gradients predicted quantum chemically by the WIEN2k code. Furthermore, an excellent correlation was found between experimental Sn-119 nuclear magnetic shielding anisotropies (determined via MAS-NMR) and calculated electric field gradients. Electronic structure calculations predict metallic properties with strong Ag-Sn bonds and also significant Ag-Ag bonding in LuAgSn. (c) 2006 Elsevier Inc. All rights reserved.
机译:通过电弧熔化和随后的退火,由这些元素合成了稀土-银-锡锡合金YAgSn,TmAgSn和LuAgSn。通过X射线粉末和单晶衍射研究了三种锡化物:NdPtSb型,P6(3)MC,Z = 2,a = 468.3(1),c = 737.2(2)pm,wR(2)= 0.0343 ,353 F-2值,YAgSn和ZrNiAl类型的12个变量,在bar 2m上的P(6),a = 726.4(2),c = 443.7(1)pm,wR(2)= 0.0399、659 F-2值,TmAgSn的15个变量,a = 723.8(2),c = 442.47(9)pm,wR(2)= 0.0674,364 F-2值,LuAgSn的15个变量。除了具有单色Mo辐射的常规实验室X射线数据外,还根据同步加速器数据(λ= 48.725 pm)对结构进行了精炼,以更精确地阐明银锡的排序。 YAgSn折叠了二维的[AgSn]网络,其Ag-Sn距离为278 pm,而TmAgSn和LuAgSn的[AgSn]网络是三维的,Ag-Sn的距离分别为279和284 pm。磁化率测量表明YaSn和LuAgSn的保利顺磁性。 TmAgSn是居里-魏斯顺磁性,实验磁矩为7.2μ(B)/ Tm。直到2K,没有明显的磁性排序。这些化合物中锡位点的局部环境通过Sn-119 Mossbauer光谱和固态NMR(在YAgSn和LuAgSn中)进行了表征,证实了结构方案中提出的锡位点多重性以及不存在Sn / Ag位点无序。发现Mossbauer四极分裂与通过WIEN2k代码化学预测的计算出的电场梯度非常吻合。此外,在实验的Sn-119核磁屏蔽各向异性(通过MAS-NMR确定)与计算出的电场梯度之间发现了极好的相关性。电子结构计算可预测具有强Ag-Sn键以及LuAgSn中显着的Ag-Ag键的金属性能。 (c)2006 Elsevier Inc.保留所有权利。

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