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Tungsten-malate interaction. Synthesis, spectroscopic and structural studies of homochiral S-malato tungstate(VI), Lambda-Na-3[WO2H(S-mal)(2)]

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Tungsten-malate interaction. Synthesis, spectroscopic and structural studies of homochiral S-malato tungstate(VI), Lambda-Na-3[WO2H(S-mal)(2)].htm (413bytes)
Date
2001-03-07
Author
Zhou, ZH
周朝晖
Wang, GF
Hou, SY
Wan, HL
万惠霖
Tsai, KR
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  • 化学化工-已发表论文 [14469]
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Abstract
Reaction of the sodium tungstate and malic acid at 1 to 2 ratio in weak acidic solution (pH 3.0-6.0) resulted in the first isolation and structural characterization of a tungsten(VI) malato complex Lambda -Na-3[WO2H(S-mal)(2)] (1) (malic acid = H(3)mal). The complex has been characterized by elemental analysis, UV and IR spectroscopy. The IR spectra are consistent with an ore-coordinated mononuclear structure as revealed by single crystal X-ray diffraction study. The tungsten atoms are quasi-octa-hedrally coordinated by two cis-oxo groups and two bidentate malate ligands via its alkoxy and alpha -carboxyl groups, while the beta -carboxylic and carboxylate groups remain uncomplexed. The latter are bonded each other through strong hydrogen bonding, forming a catenarian chain, and the anions are connected in homochiral form. It is proposed that the chiral configuration of metal center in wild-type FeMo-co biosynthesis might be induced by the coordination of the chiral R-homocitric acid, while a mixture of raceme might be obtained in the biosynthesis of NifV-FeMo-cofactor. (C) 2001 Elsevier Science B.V. All rights reserved.
Citation
INORGANICA CHIMICA ACTA,2001,314(1-2):184-188
URI
http://dx.doi.org/10.1016/S0020-1693(00)00392-3
https://dspace.xmu.edu.cn/handle/2288/12678

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