Syntheses, crystal structures and biological relevance of glycolato and S-lactato molybdates
Glycolato and S-lactato complexes containing the dioxomolybdenum(VI) moiety have been synthesized for studies on the role of the α-hydroxycarboxylato anion in the iron molybdenum cofactor of nitrogenase. The ligands in these complexes, vis K 2[MoO 2(glyc) 2] · H 2O (H 2glyc=glycolic acid, C 2H 4O 3)...
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Published in | Journal of inorganic biochemistry Vol. 98; no. 6; pp. 1037 - 1044 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.06.2004
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Subjects | |
Online Access | Get full text |
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Summary: | Glycolato and
S-lactato complexes containing the dioxomolybdenum(VI) moiety have been synthesized for studies on the role of the α-hydroxycarboxylato anion in the iron molybdenum cofactor of nitrogenase. The ligands in these complexes, vis K
2[MoO
2(glyc)
2]
·
H
2O (H
2glyc=glycolic acid, C
2H
4O
3) (
1) and {Na
2[MoO
2(
S-lact)
2]}
3
·
13H
2O (H
2lact=lactic acid, C
3H
6O
3) (
2) chelate through their α-alkoxyl and α-carboxyl oxygen atoms. In contrast, octanuclear K
6[(MoO
2)
8(glyc)
6(Hglyc)
2]
·
10H
2O (
3) formed by the reduction of the glycolato complex (
1), features three different ligand binding modes: (i) non-bridging and bridging bidentate coordination of α-alkoxyl and α-carboxyl groups, and (ii) bidentate bridging using α-carboxyl group, leaving the α-alkoxyl group free. The octanuclear skeleton shows strong metal–metal interactions. The coordination modes in (
1) and (
2) mimic that of homocitrate to the iron molybdenum cofactor (FeMo-co) of nitrogenase. The bidentate coordination of α-alkoxyl and α-carboxyl groups shows that bond of α-carboxyl group to Mo is less susceptible to the oxidation state of molybdenum compared with the Mo-α-alkoxyl bond. This is supported by the dinuclear coordination of α-carboxyl group with free α-alkoxyl group in glycolato molybdate(V) (
3). |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0162-0134 1873-3344 |
DOI: | 10.1016/j.jinorgbio.2004.02.024 |