Maggard Paul A, Corbett John D
Department of Chemistry, Iowa State University, Ames, Iowa 50011, USA.
Inorg Chem. 2004 Apr 19;43(8):2556-63. doi: 10.1021/ic0303136.
Y(5)M(2)Te(2) (M = Fe, Co, Ni) have been prepared by high-temperature solid-state techniques and shown to be isostructural and orthorhombic Cmcm (No. 63), Z = 4. The structure was established by single crystal X-ray methods at 23 degrees C for M = Fe, with a = 3.9594(3) A, b = 15.057(1) A, and c = 15.216(1) A. The new structure contains zigzag chains of the late transition metal sheathed by a column of yttrium atoms that are in turn condensed through trans vertices on the latter to yield 2D bimetallic layers separated by single layers of tellurium atoms. Reaction of hydrogen with Y(5)Ni(2)Te(2) causes a rumpling of the Y-Ni layers as determined by both single X-ray crystal means at 23 degrees C and neutron powder diffraction at -259 degrees C for Y(5)Ni(2)Te(2)D(0.41(1)), Pnma (No. 62), Z = 4. Lattice constants from the former study are a = 14.3678(7) A, b = 4.0173(2) A, and c = 15.8787(7) A. The hydrogen is accommodated in tetrahedral yttrium cavities generated by bending the formerly flat sheets at the trans Y vertices. A higher hydride version also exists. Band structure calculations confirm the 2D metal-bonded character of the compounds and also help illustrate the bonding/matrix changes that accompany the bonding of hydrogen. The ternary structures for both Y(5)M(2)Te(2) and Sc(5)Ni(2)Te(2) can be derived from that of Gd(3)MnI(3), the group illustrating three different kinds of metal chain condensation.
Y(5)M(2)Te(2)(M = Fe、Co、Ni)已通过高温固态技术制备出来,并显示为同构且属于正交晶系Cmcm(编号63),Z = 4。通过单晶X射线方法在23摄氏度下确定了M = Fe时的结构,a = 3.9594(3) Å,b = 15.057(1) Å,c = 15.216(1) Å。新结构包含由一列钇原子包覆的晚期过渡金属的锯齿链,这些钇原子又通过后者上的反式顶点凝聚,形成由单层碲原子分隔的二维双金属层。氢气与Y(5)Ni(2)Te(2)反应会导致Y - Ni层起皱,这在23摄氏度下通过单晶X射线晶体方法以及在 - 259摄氏度下对Y(5)Ni(2)Te(2)D(0.41(1))进行中子粉末衍射均已确定,其属于Pnma(编号62),Z = 4。前一项研究得到的晶格常数为a = 14.3678(7) Å,b = 4.0173(2) Å,c = 15.8787(7) Å。氢被容纳在通过在反式Y顶点处弯曲先前的平面片而产生的四面体钇空穴中。还存在更高氢化物版本。能带结构计算证实了这些化合物的二维金属键合特性,也有助于说明伴随氢结合的键合/基体变化。Y(5)M(2)Te(2)和Sc(5)Ni(2)Te(2)的三元结构都可以从Gd(3)MnI(3)的结构推导而来,该族展示了三种不同类型的金属链凝聚。