Barrier N, Fontaine B, Pierrefixe S, Gautier R, Gougeon P
Laboratoire CRISMAT, UMR CNRS 6508, 6, Boulevard Marechal Juin 14050 CAEN Cedex 4, France.
Inorg Chem. 2009 Apr 20;48(8):3848-56. doi: 10.1021/ic801942d.
The novel quaternary reduced molybdenum oxides LaR(4)Mo(36)O(52) (R = Dy, Er, Yb, and Y) have been synthesized with solid-state reactions at 1400 degrees C for 48 h in sealed molybdenum crucibles. The crystal structure was determined on a single crystal of LaEr(4)Mo(36)O(52) by X-ray diffraction. LaEr(4)Mo(36)O(52) crystallizes in the tetragonal space group I4 with two formula units per cell and the following lattice parameters: a = 19.8348(2) and c = 5.6594(1) A. The Mo network is dominated by infinite chains of trans-edge-shared Mo(6) octahedra, which coexist with Mo(2) pairs and rectangular Mo(4) clusters. The Mo-Mo distances within the infinite chains range from 2.5967(7) to 2.8529(8) A and from 2.239(3) to 2.667(2) A in the Mo(2) pairs and rectangular Mo(4) clusters, respectively. The Mo-O distances are comprised between 1.993(7) and 2.149(7) A, as usually observed in these types of compound. The La(3+) and Er(3+) ions are in a square-prismatic [LaO(8)] and a tricapped trigonal-prismatic [ErO(9)] environment of oxygen atoms, respectively. The La-O distances range from 2.555(6) to 2.719(6) A and the Er-O ones from 2.260(6) to 2.469(5) A. Theoretical calculations allow the determination of the optimal electron count of both motifs in the title compound. Weak interactions occur between neighboring dimetallic and tetrametallic clusters and between trans-edge-sharing infinite chains and dimers and tetramers. The presence of rectangular clusters is favored on the basis of theoretical considerations. Single-crystal resistivity measurements show that LaEr(4)Mo(36)O(52) is metallic between 4.2 and 300 K, in agreement with the band structure calculations. Magnetic susceptibility measurements indicate that the oxidation state of the magnetic rare earths is +3, and there is an absence of localized moments on the Mo network.
新型四元低价钼氧化物LaR₄Mo₃₆O₅₂(R = 镝、铒、镱和钇)通过在密封钼坩埚中于1400℃进行48小时的固态反应合成。通过X射线衍射在LaEr₄Mo₃₆O₅₂的单晶上确定了晶体结构。LaEr₄Mo₃₆O₅₂结晶于四方空间群I4,每个晶胞中有两个化学式单元,其晶格参数如下:a = 19.8348(2) Å,c = 5.6594(1) Å。钼网络主要由通过边共享的Mo₆八面体的无限链组成,这些链与Mo₂对和矩形Mo₄簇共存。无限链内的Mo - Mo距离范围为2.5967(7)至2.8529(8) Å,Mo₂对和矩形Mo₄簇中的Mo - Mo距离分别为2.239(3)至2.667(2) Å。Mo - O距离在1.993(7)至2.149(7) Å之间,这在这类化合物中是常见的。La³⁺和Er³⁺离子分别处于由氧原子构成的方形棱柱形[LaO₈]和三帽三棱柱形[ErO₉]环境中。La - O距离范围为2.555(6)至2.719(6) Å,Er - O距离范围为2.260(6)至2.469(5) Å。理论计算能够确定标题化合物中两种结构基元的最佳电子数。相邻的双金属和四金属簇之间以及通过边共享的无限链与二聚体和四聚体之间存在弱相互作用。基于理论考虑,矩形簇的存在更有利。单晶电阻率测量表明LaEr₄Mo₃₆O₅₂在4.2至300 K之间是金属性的,这与能带结构计算结果一致。磁化率测量表明磁性稀土的氧化态为 +3,并且钼网络上不存在局域磁矩。