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Book ChapterDOI

The Coordination and Bioinorganic Chemistry of Molybdenum

09 Mar 2007-pp 1-223
About: The article was published on 2007-03-09. It has received 78 citations till now. The article focuses on the topics: Bioorganometallic chemistry & Bioinorganic chemistry.
Citations
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Journal ArticleDOI
TL;DR: The 2011 WHO Guidelines for Drinking-Water Quality (fourth edition) advised a health-based value of 70μg/L for Mo but this is no longer promulgated as a formal guideline value as WHO consider such concentrations to be rarely found in drinking water as discussed by the authors.

196 citations

Journal ArticleDOI
Russ Hille1
TL;DR: An overview of the current state of our understanding of the molybdenum-containing enzyme xanthine oxidoreductase is presented, with an emphasis on work done in the past five years.
Abstract: An overview of the current state of our understanding of the reaction mechanism of the molybdenum-containing enzyme xanthine oxidoreductase is presented, with an emphasis on work done in the past five years Recent studies of the biosynthesis of the pterin cofactor bound to the metal in the active site are also reviewed, as is crystallographic work that has clarified the coordination geometry of the molybdenum center This structural work provides the context in which to understand recent mechanistic studies of the enzyme, in particular those aimed at elucidating the role of specific amino acid residues in the active site of the enzyme(© Wiley-VCH Verlag GmbH & Co KGaA, 69451 Weinheim, Germany, 2006)

119 citations

Journal ArticleDOI
TL;DR: In this article, synthetic aspects of molybdenum sulfide-based materials were reviewed, with emphasis on the catalytic materials, and a number of preparation methods were critically compared, including molecular precursor decomposition, hydrothermal, soft chemistry aqueous, surfactant-aided, intercalation-exfoliation, and solid gas reactions.

114 citations

Journal ArticleDOI
TL;DR: The ability of Desulfovibrio desulfuricans formate dehydrogenase (DdFDH) to reduce carbon dioxide was kinetically and mechanistically characterized and a kinetic model of a hysteretic enzyme is proposed to interpret and predict the progress curves of the Dd FDH-catalyzed reactions.
Abstract: Carbon dioxide accumulation is a major concern for the ecosystems, but its abundance and low cost make it an interesting source for the production of chemical feedstocks and fuels. However, the thermodynamic and kinetic stability of the carbon dioxide molecule makes its activation a challenging task. Studying the chemistry used by nature to functionalize carbon dioxide should be helpful for the development of new efficient (bio)catalysts for atmospheric carbon dioxide utilization. In this work, the ability of Desulfovibrio desulfuricans formate dehydrogenase (Dd FDH) to reduce carbon dioxide was kinetically and mechanistically characterized. The Dd FDH is suggested to be purified in an inactive form that has to be activated through a reduction-dependent mechanism. A kinetic model of a hysteretic enzyme is proposed to interpret and predict the progress curves of the Dd FDH-catalyzed reactions (initial lag phase and subsequent faster phase). Once activated, Dd FDH is able to efficiently catalyze, not only t...

103 citations

Journal ArticleDOI
TL;DR: The mesoporous molecular sieve MCM-41 was covalently grafted with 3-aminopropyl trimethoxysilane (AmpMCM41) in this article.
Abstract: The mesoporous molecular sieve MCM-41 was covalently grafted with 3-aminopropyl trimethoxysilane to give aminopropyl modified MCM-41 (AmpMCM-41). Reaction of this material with furfural, pyrrolcarbaldehyde, 2-acetylpyrrol, 2-aminoacetophenone, salicylaldehyde and acetylacetone afforded the corresponding supported Schiff base ligands. Subsequent reaction with bis(acetylacetonato)dioxomolybdenum(VI) leads to various molybdenum complexes supported on MCM-41 through propyl chain spacer. Characterization of these materials was carried out with FT-IR, atomic absorption spectroscopy, powder X-ray diffraction (XRD) and BET nitrogen adsorption–desorption methods. The XRD and BET analyses revealed that textural properties of support were preserved during the grafting experiments. The resultant materials successfully catalyzed the epoxidation of cyclooctene, cyclohexene, 1-hexene and 1-octene with tert -butyl hydroperoxide (TBHP) to the corresponding epoxides with 98–100% selectivities.

92 citations

References
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Journal ArticleDOI
TL;DR: Molybdenum-deficient plants transferred to 185WO4=, incorporate W in protein fractions, normally associated with nitrate reductase (NR.).

102 citations

Book ChapterDOI
TL;DR: In this paper, the authors describe different types of peroxide in transition metal peroxides and the properties of the peroxide linked to the metal by directed bonds and are closely related to the oxygenated O2-carrying complexes.
Abstract: Publisher Summary This chapter describes different types of peroxide. The solid hydrated peroxides of elements such as copper, praseodymium, or cerium may well contain O2–ions: the only roughly stoichiametric peroxides of thorium and plutonium represent a slightly different class of compound, but may still be essentially ionic. The peroxides of transition metals either in complexes or in high oxidation states (or in both), however, contain peroxide linked to the metal by directed bonds, and are closely related to the oxygenated O2-carrying complexes. The characteristic and interesting properties of transition metal complexes are largely associated with compounds of the last two classes. Most of the known transition metal peroxides have been obtained by the action of H2O2 on some derivative of the metal; in aqueous solution, the proportion of peroxide in the product increases with increasing pH, though this may not be true in solvents other than water. Peroxides of rhenium and cobalt, and of course the oxygenated O2-carrying species containing iron, iridium, or copper, have been made from O2 instead of H2O2; there is evidence that peroxy derivatives of uranium have been obtained by heating compounds of uranium in air, while peroxides are often postulated as unstable intermediates in the oxidation by air of such species as chromium.

97 citations