Coordination and valence of europium in [Eu(α-2-As2W17O61)2]17- and [Eu(W5O18)2]9-

被引:18
作者
Antonio, MR
Soderholm, L
Jennings, G
Francesconi, LC
Dankova, M
Bartis, J
机构
[1] Argonne Natl Lab, Div Chem, Argonne, IL 60439 USA
[2] CUNY Hunter Coll, Dept Chem, New York, NY 10021 USA
基金
美国国家卫生研究院;
关键词
europium; L-3; edge; X-ray absorption fine structure; spectroelectrochemistry; valency; polyoxometalate; heteropolyanion;
D O I
10.1016/S0925-8388(98)00450-2
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Europium L-3 edge X-ray absorption fine structure (XAFS) spectroelectrochemistry was used to determine the valence of europium in [Eu(alpha-2-As2W17O61)(2)](17-) and [Eu(W5O18)(2)](9-). Dilute solutions of these anions in aqueous supporting electrolytes were examined at ambient temperature and at extreme potentials. In situ XANES (X-ray absorption near edge structure) data revealed that Eu is trivalent in both [Eu(alpha-2-As2W17O61)(2)](17-) and [Eu(W5O18)(2)](9-) at rest potential. Furthermore, it was not reduced to Eu2+ by constant-potential bulk electrolysis at significantly reducing potentials under the electrochemical conditions used herein. These results stand in obvious contrast to the redox behavior of [EuP5W30O110](12-), in which Eu3+ is reduced to Eu2+ under similar electrochemical conditions. (C) 1998 Elsevier Science S.A.
引用
收藏
页码:827 / 830
页数:4
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