Search results for "Molybdenum"

Metal complexes of an amine bisphenol with a thiophene side-arm

2010

Dioxomolybdenum(VI) and oxotungsten(VI) complexes with a new amine bisphenol ligand (H2L) are reported. The ligand which carries a neutral nitrogen atom, two phenolic oxygen atoms and a thiophene side-arm was synthesized by a simple one-pot Mannich reaction. Further reaction with [MoO2(acac)2] yielded a monomeric molybdenum complex [MoO2(L)(MeOH)] (2a) or a dimeric complex [Mo2O2(μ-O)2(L)2] (2b), depending on the reaction conditions. The reaction with a tungsten trisglycolate [W(eg)3] led to the formation of a monomeric compound [WO(eg)(L)] (3). In these complexes, the potentially tetradentate amine bisphenolate dianion coordinates as a tridentate O,N,O donor while the sulfur side-arm donor…

Impact on Glucose Homeostasis: Is Food Biofortified with Molybdenum a Workable Solution? A Two-Arm Study

2022

Diabetes is expected to increase up to 700 million people worldwide with type 2 diabetes being the most frequent. The use of nutritional interventions is one of the most natural approaches for managing the disease. Minerals are of paramount importance in order to preserve and obtain good health and among them molybdenum is an essential component. There are no studies about the consumption of biofortified food with molybdenum on glucose homeostasis but recent studies in humans suggest that molybdenum could exert hypoglycemic effects. The present study aims to assess if consumption of lettuce biofortified with molybdenum influences glucose homeostasis and whether the effects would be due to c…

MoVReagents in Organic Synthesis (Eur. J. Org. Chem. 11/2016)

2016

8-Hydroxyquinoline-2-Carboxylic Acid as Possible Molybdophore: A Multi-Technique Approach to Define Its Chemical Speciation, Coordination and Sequest…

2020

8-hydroxyquinoline-2-carboxylic acid (8-HQA) has been found in high concentrations (0.5&ndash

"Partial oxidation of methane and methanol on FeOx-, MoOx- and FeMoOx -SiO2 catalysts prepared by sol-gel method: a comparative study"

2020

[EN] FeOx-, MoOx and FeMoOx-SiO2 materials prepared by a sol-gel procedure have been evaluated as catalysts for the partial oxidation of methane and methanol. The effect of decreasing the pH of the synthesis gel on the chemical nature of FeOx and MoOx species has been investigated. Characterization results show that low pH improves the dispersion of metal oxide species present in SiO2 matrix. For FeOx/SiO2 materials, the presence of dispersed FeOx species (rather than bulk Fe2O3) improves the selectivity to formaldehyde in the partial oxidation of methane and methanol. For FeMoOx/SiOx catalysts, dispersed species favor the selectivity to formaldehyde only for methane oxidation. In contrast,…

Snapshots of the Formation of Inorganic MoS2 Onion-Type Fullerenes: A “Shrinking Giant Bubble” Pathway

2010

Direct identification of 103–107Mo by a rapid chemical separation procedure

1977

Abstract The nuclides 103–107Mo have been identified by means of γ-ray spectroscopy after the separation of molybdenum from fission products of 235U and 239Pu by a rapid chemical procedure. Half-lives of 67.5 ± 1.5 s for 103Mo, 59.4 ± 0.8 s for 104Mo, 36.7 ± 1.0 s for 105Mo, 8.4 ± 0.5 s for 106Mo and 3.5 ± 0.5 s for 107Mo have been determined and the main γ-lines were assigned to the decay of these isotopes. Some evidence for 108Mo with a half-life ≤2 s has also been obtained.

Effects of substitutions on cyclopentadienyl rings in complexes with molybdenum-mercury bonds. 95Mo and 199Hg NMR studies

1995

NMR data for 95Mo and 199Hg nuclei have been obtained for new di- and trimetallic complexes Cp′(CO)3MoHgX containing molybdenum-mercury bonds and bulky and/or potentially bifunctional substituted cyclopentadienyl ligands; Cp′=C5HMe2Ph2, C5Me4Bz, C5Bz5, C5H4PPh2 and C5Me4PPh2 (Bz=CH2C6H5; Me =CH3; Ph=C6H5); X=Cp′(CO)3Mo, Cl, Br, 1, SCN. They are discussed within the context of our earlier results reported for analogous complexes with the cyclopentadienyl ligands bearing methyl groups. With the exception of phenyl substituted rings, a rather narrow range of 95Mo chemical shifts is found for the compounds with the same number of different substituents on cyclopentadienyl ligands. An outstandin…

The role of molybdenum in Mo-doped V–Mg–O catalysts during the oxidative dehydrogenation of n-butane

1999

Abstract A detailed study on the influence of the addition of molybdenum ions on the catalytic behaviour of a selective vanadium–magnesium mixed oxide catalyst in the oxidation of n-butane has been performed. The catalysts have been prepared by impregnation of a calcined V–Mg–O mixed oxides (23.8 wt% of V2O5) with an aqueous solution of ammonium heptamolybdate, and then calcined, and further characterised by several physico-chemical techniques, i.e. SBET, XRD, FTIR, FT-Raman, XPS, H2-TPR. MgMoO4, in addition to Mg3V2O8 and MgO, have been detected in all the Mo-doped samples. The incorporation of molybdenum modifies not only the number of V5+-species on the catalyst surface and the reducibil…

MoO (x≤2) ultrathin film growth from reactions between metallic molybdenum and TiO2 surfaces

2001

Abstract Exposures to oxygen at room temperature and annealings under vacuum were carried out on deposits obtained from molybdenum interacting with (1 1 0) TiO 2 surfaces in order to obtain molybdenum oxide ultra thin films. Exposures to oxygen at room temperature show that the interfacial molybdenum oxide layers resulting from the TiO 2 /Mo interactions are inactive towards oxygen whereas the metallic molybdenum clusters, which grew on top of the interfacial layers, oxidise into MoO 3 . Besides, during annealings under vacuum, substrate oxygen anions can diffuse into the deposit. Thus, between 400 and 500°C, molybdenum oxide layers are progressively oxidised into MoO 2 . Moreover, from the…