Protonation and methylation of an anderson-type polyoxoanion [IMo6O24]5-

被引:33
作者
Honda, Daisuke
Ikegami, Shusaku
Inoue, Tomoaki
Ozeki, Tomoji [1 ]
Yagasaki, Atsushi
机构
[1] Tokyo Inst Technol, Dept Chem & Mat Sci, Tokyo 1528551, Japan
[2] Kwansei Gakuin Univ, Dept Chem, Sanda 6691337, Jamaica
关键词
D O I
10.1021/ic061881z
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A series of protonated and methylated Anderson-type molybdoperiodates as well as the unprotonated [IMo6O24](5-) have been synthesized and structurally characterized as tetra-n-butylammonium salts: [(n-C4H9)(4)N](5)[IMo6O24] [monoclinic, space group C2/c, a = 33.6101(3) A, b = 15.2575(1) A, c = 24.0294(2) A, beta = 126.9569(3)degrees, Z = 4], [(n-C4H9)(4)N](4)[IMo6O23(OH)] [monoclinic, space group P2(1)/c, a = 9.5587(1) A, b = 24.1364(2) A, c = 18.2788(2) A, beta = 90.1562(5)degrees, Z = 2], [(n-C4H9)(4)N](3)[IMo6O22(OH)(2)]center dot 2DMF [monoclinic, space group P2(1)/a, a = 17.6105(4) A, b = 15.5432(5) A, c = 29.3316(9) A, beta = 91.475(3)degrees, Z = 4], [(n-C4H9)(4)N](4)[IMo6O23(OMe)]center dot 3H(2)O [orthorhombic, space group Pbca, a = 17.0679(4) A, b = 25.6998(6) A, c = 20.7428(4) A, Z = 4], [(n-C4H9)(4)N](3)[IMo6O22(OMe)(2)] [monoclinic, space group P2(1)/n, a = 10.4009(1) A, b = 14.6658(3) A, c = 23.5395(4) A, beta = 100.324(1)degrees, Z = 2]. In all of these compounds, the [IMo6O24](5-) anion is protonated or methylated selectively at O atoms shared by two Mo atoms. The results have also revealed that the protonated Anderson-type molybdoperiodates readily react with methanol in a very selective manner, while the unprotonated [IMo6O24](5-) anion does not react with methanol under similar conditions.
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页码:1464 / 1470
页数:7
相关论文
共 60 条
[21]   MOLECULAR-CONFIGURATION OF DECANIOBATE ION (NB10O28(6-)) [J].
GRAEBER, EJ ;
MOROSIN, B .
ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE, 1977, 33 (JUL15) :2137-2143
[22]   CRYSTAL-STRUCTURE OF TETRACAESIUMDIHYDROGENDECAVANADATE TRIHYDRATE, CS4H2V10O28-CENTER-DOT-3H2O - A LAYERED CRYSTAL-STRUCTURE OF DECAVANADATE [J].
HASHIMOTO, M ;
MISONO, M ;
HIBINO, M ;
OI, J ;
KUDO, T .
POLYHEDRON, 1993, 12 (22) :2745-2747
[23]   Methoxide of an Anderson-type polyoxometalate and its conversion to a new type of species, [IMo9O32(OH)(OH2)3]4- [J].
Honda, D ;
Ozeki, T ;
Yagasaki, A .
INORGANIC CHEMISTRY, 2005, 44 (26) :9616-9618
[24]   Novel structural aspects of oxythiamine, an antagonist of thiamine.: Crystal structures of three salts, (oxythiamineH)(picrolonate)2•2H2O, (oxythiamineH)(PtCl6), (oxythiamineH)2(V10O28H2) •8H2O, and a metal complex Pt(oxythiamine)Cl3•H2O [J].
Hu, NH ;
Tokuno, T ;
Aoki, K .
INORGANICA CHIMICA ACTA, 1999, 295 (01) :71-83
[25]  
Hur N., 1990, INORG SYNTH, V27, P78
[26]   Electron polarisation [J].
Keggin, JF .
NATURE, 1933, 131 :908-909
[27]   RELATIVE BASICITIES OF THE OXYGEN SITES IN [V10O28]6- - AN ANALYSIS OF THE ABINITIO DETERMINED DISTRIBUTIONS OF THE ELECTROSTATIC POTENTIAL AND OF THE LAPLACIAN OF CHARGE-DENSITY [J].
KEMPF, JY ;
ROHMER, MM ;
POBLET, JM ;
BO, C ;
BENARD, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (04) :1136-1146
[28]   Synthesis and characterization of materials containing arrays of decavanadate clusters [J].
Khan, I ;
Ayesh, S ;
Yohannes, E ;
Doedens, RJ .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2003, 8 :A177-A184
[29]  
Khenkin AM, 2002, ADV SYNTH CATAL, V344, P1017, DOI 10.1002/1615-4169(200210)344:9<1017::AID-ADSC1017>3.0.CO
[30]  
2-X