Metal ion complexes derived from the α1 isomer of (P2W17O61)10-:: comparison with the corresponding α1 species

被引:90
作者
Keita, B
Girard, F
Nadjo, L
Contant, R
Canny, J
Richet, M
机构
[1] Univ Paris Sud, CNRS, UMR 8610, Lab Physicochim Rayonnements, F-91405 Orsay, France
[2] Univ Paris 06, CNRS, UPRESA 7071, Lab Chim Inorgan & Mat Mol, F-75252 Paris 05, France
来源
JOURNAL OF ELECTROANALYTICAL CHEMISTRY | 1999年 / 478卷 / 1-2期
关键词
polyoxometalates; substituted heteropolyanions; Dawson-type structure; alpha(1) and alpha(2) isomers; first transition metal cations;
D O I
10.1016/S0022-0728(99)00414-3
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The lacunary alpha(1)- and alpha(2)-[P2W17O61](10-) isomers derived from the Dawson molecule [alpha P2W18O62](10-) have been used as ligands for the following metal cations: Ca-II V-V, Mn-II, Fe-III, Co-II, Ni-II, Cu-II, Zn-II, and Mo-VI, respectively. We have succeeded in obtaining pure samples of stable compounds of the sc, series. The cyclic voltammograms of these lacunary precursor species as well as those of the substituted complexes have been run in a pH 3 medium with the aim of finding out distinctive features from one series to the nest. Several compounds of the alpha(2) series are known to be stable and can, therefore, serve eventually as references to distinguish the two series. For the alpha(2) compounds, the first two two-electron processes are followed by a set of two, presumably one-electron steps. and this fingerprint is observed throughout the series, except for the copper and the molybdenum derivatives. These last two complexes can, however, be identified by other specific features. As another general observation on shifting from the sc, to the a, series, it is found also that the peak potential of the first tungsten wave is driven in the negative direction. Finally, a simple rationale is offered for the whole set of observations. (C) 1999 Elsevier Science S.A. All rights reserved.
引用
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页码:76 / 82
页数:7
相关论文
共 36 条
[1]  
ACCERETE R, 1979, J CHEM SOC CHEM COMM, P777
[2]   A NEW GENERAL STRUCTURAL CATEGORY OF HETEROPOLYELECTROLYTES . UNUSUAL MAGNETIC AND THERMAL CONTRACTION PHENOMENA [J].
BAKER, LCW ;
BAKER, VS ;
ERIKS, K ;
POPE, MT ;
SHIBATA, M ;
ROLLINS, OW ;
FANG, JH ;
KOH, LL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1966, 88 (10) :2329-&
[3]   Preparation and tungsten-183 NMR characterization of [alpha-1-P2W17O61](10-), [alpha-1-Zn(H2O)P2W17O61](8-), and [alpha-2-Zn(H2O)P2W17O61](8-) [J].
Bartis, J ;
Kunina, Y ;
Blumenstein, M ;
Francesconi, LC .
INORGANIC CHEMISTRY, 1996, 35 (06) :1497-1501
[4]   Lanthanide complexes of the α-1 isomer of the [P2W17O61]10- heteropolytungstate:: Preparation, stoichiometry, and structural characterization by 183W and 31P NMR spectroscopy and europium(III) luminescence spectroscopy [J].
Bartis, J ;
Dankova, M ;
Lessmann, JJ ;
Luo, QH ;
Horrocks, WD ;
Francesconi, LC .
INORGANIC CHEMISTRY, 1999, 38 (06) :1042-1053
[5]   HETEROPOLYBLUES - RELATIONSHIP BETWEEN METAL-OXYGEN-METAL BRIDGES AND REDUCTION BEHAVIOR OF "OCTADECA(MOLYBDOTUNGSTO)DIPHOSPHATE ANIONS [J].
CIABRINI, JP ;
CONTANT, R ;
FRUCHART, JM .
POLYHEDRON, 1983, 2 (11) :1229-1233
[6]   STEREOSPECIFIC PREPARATIONS OF NEW N-MOLYBDO-(18-N)-TUNGSTO-2-PHOSPHATES AND RELATED DEFECT COMPOUNDS (N=2, 4 OR 5) [J].
CONTANT, R ;
CIABRINI, JP .
JOURNAL OF INORGANIC & NUCLEAR CHEMISTRY, 1981, 43 (07) :1525-1528
[7]   Iron-substituted Dawson-type tungstodiphosphates: Synthesis, characterization, and single or multiple initial electronation due to the substituent nature or position [J].
Contant, R ;
Abbessi, M ;
Canny, J ;
Belhouari, A ;
Keita, B ;
Nadjo, L .
INORGANIC CHEMISTRY, 1997, 36 (22) :4961-4967
[8]  
Contant R., 1977, J CHEM RES S, P222
[9]  
CONTANT R, UNPUB EUR J INORG CH
[10]  
CONTANT R, 1990, INORG CHEM, V27, P107