Synthesis, Crystal and Electronic Structures, and Physical Properties of the Novel Compounds LaR4Mo36O52 (R = Dy, Er, Yb, and Y) Containing Infinite Chains of Trans-Edge-Shared Mo6 Octahedra and Mo2 Pairs and Rectangular Mo4 Clusters with Triple Mo-Mo Bonds

被引:4
作者
Barrier, N. [2 ]
Fontaine, B. [1 ]
Pierrefixe, S. [1 ]
Gautier, R. [1 ]
Gougeon, P. [1 ]
机构
[1] Univ Rennes 1, Ecole Natl Super Chim Rennes, CNRS, UMR 6226, F-35042 Rennes, France
[2] CNRS, UMR 6508, Lab CRISMAT, F-14050 Caen 4, France
关键词
REDUCED MOLYBDENUM OXIDES; ND; PR; CE; REFINEMENT; LAMO8O14; FORM; R=LA; ION; SM;
D O I
10.1021/ic801942d
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The novel quaternary reduced molybdenum oxides LaR4Mo36O52 (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 LaEr4Mo36O52 by X-ray diffraction. LaEr(4)Mo(36)o(52) crystallizes in the tetragonal space group I (4) over bar with two formula units per cell and the following lattice parameters: a = 19.8348(2) and c = 5.6594(1) angstrom. 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) angstrom and from 2.239(3) to 2.667(2) angstrom 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) angstrom, as usually observed in these types of compound. The La3+ and Er3+ ions are in a square-prismatic [LaO8] and a tricapped trigonal-prismatic [ErO9] environment of oxygen atoms, respectively. The La-O distances range from 2.555(6) to 2.719(6) angstrom 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 LaEr4Mo36O52 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.
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页码:3848 / 3856
页数:9
相关论文
共 50 条
[1]  
Albright T. A., 1985, ORBITAL INTERACTION
[2]   SIR97:: a new tool for crystal structure determination and refinement [J].
Altomare, A ;
Burla, MC ;
Camalli, M ;
Cascarano, GL ;
Giacovazzo, C ;
Guagliardi, A ;
Moliterni, AGG ;
Polidori, G ;
Spagna, R .
JOURNAL OF APPLIED CRYSTALLOGRAPHY, 1999, 32 :115-119
[3]   AN EMPIRICAL CORRECTION FOR ABSORPTION ANISOTROPY [J].
BLESSING, RH .
ACTA CRYSTALLOGRAPHICA SECTION A, 1995, 51 :33-38
[4]   CRYSTAL STRUCTURE OF NIOBIUM MONOXIDE [J].
BOWMAN, AL ;
WALLACE, TC ;
YARNELL, JL ;
WENZEL, RG .
ACTA CRYSTALLOGRAPHICA, 1966, 21 :843-&
[5]   CHARACTERIZATION OF TRINEGATIVE OCTACHLORODITECHNETATE ION [J].
BRATTON, WK ;
COTTON, FA .
INORGANIC CHEMISTRY, 1970, 9 (04) :789-&
[6]   OCTACHLORODIMOLYBDATE(2) ION . A NEW SPECIES WITH A QUADRUPLE METAL-METAL BOND [J].
BRENCIC, JV ;
COTTON, FA .
INORGANIC CHEMISTRY, 1969, 8 (01) :7-&
[7]   EMPIRICAL PARAMETERS FOR CALCULATING CATION-OXYGEN BOND VALENCES [J].
BROWN, ID ;
WU, KK .
ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE, 1976, 32 (JUL15) :1957-1959
[8]  
BURNUS R, 1987, Z NATURFORSCH B, V42, P536
[9]   SYNTHESIS, STRUCTURE AND PROPERTIES OF MN1.5MO8O11, A UNIQUE STRUCTURE TYPE AMONG COMPOUNDS HAVING INFINITE CHAINS OF TRANS-EDGE-SHARED OCTAHEDRAL CLUSTER UNITS [J].
CARLSON, CD ;
BROUGH, LF ;
EDWARDS, PA ;
MCCARLEY, RE .
JOURNAL OF THE LESS-COMMON METALS, 1989, 156 :325-339
[10]   CRYSTAL AND MOLECULAR STRUCTURE OF DIPOTASSIUM OCTACHLORODIRHENATE(3) DIHYDRATE K2[RE2CL8].2H2O [J].
COTTON, FA ;
HARRIS, CB .
INORGANIC CHEMISTRY, 1965, 4 (03) :330-&