Search results for "OXIDATION"

showing 10 items of 1913 documents

Interface charge density matching as driving force for new mesostructured oxovanadium phosphates with hexagonal structure, [CTA]xVOPO4·zH2O

1999

Hexagonal mesostructured mixed-valence oxovanadium phosphates [CTA]xVOPO4·zH2O, in short ICMUV-2, have been synthesized through a S+I- cooperative mechanism using cationic surfactant (cetyltrimethylammonium, CTAB) rodlike micelles as a template. On the lines of the hypothesis that the driving force leading to the formation of mesostructured solids is the charge density matching at the interface between the supramolecular−organic and supramolecular−inorganic moieties, the self-assembling process between CTA+ micelles and VOPO4q- planar anions can be thought of as consequence of the adequate adjustment of the metal mean oxidation state. X-ray powder diffraction and TEM techniques show that th…

StereochemistryChemistryGeneral Chemical EngineeringCharge densityGeneral ChemistryMicelleMetalCrystallographyOxidation statevisual_artX-ray crystallographyMaterials Chemistryvisual_art.visual_art_mediumMesoporous materialHydratePowder diffraction
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Molecular materials with conducting and magnetic properties based on ET and [ M(tdas)2]x-dithiolenes

2004

Two hybrid molecular materials showing a combination of magnetic and conducting properties, the charge-transfer (ET) 2 [Fe(tdas) 2 ] (1) and (ET)Ni(tdas) 2 (2), (ET=bis(ethylenedithio) tetrathiafulvalene; M=Fe, Ni; tdas=l,2,5-thiadiazole-3,4-dithiolate) salts, are characterized by vibrational (IR and Raman) and UV-VIS-NIR spectroscopies. These studies have proved to be effective and diagnostic tools in identifying the oxidation state (partial or integer) and the packing pattern (dimers or segregated stacks) of the ET donor only, since no v(C=C) group vibration sensitive to the charge of M(tdas) 2 complexes has been observed. This is ascribed to the extensive electron-delocalization inside t…

StereochemistryChemistryIntermolecular forceGeneral Physics and AstronomyRing (chemistry)Extended Hückel methodCrystallographysymbols.namesakechemistry.chemical_compoundElectrical resistivity and conductivityOxidation stateMolecular vibrationsymbolsRaman spectroscopyTetrathiafulvaleneJournal de Physique IV (Proceedings)
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Membrane D-lactate oxidase in Zymomonas mobilis: evidence for a branched respiratory chain.

1998

Respiratory chain composition of the ethanol-producing bacterium Zymomonas mobilis was studied. Its membrane D-lactate oxidase was characterised. With NADH, but not D-lactate as substrate, a cytochrome o-like component was seen in CO difference spectra. Chlorpromazine specifically inhibited reduction of cytochrome d, while myxothiazol eliminated the cytochrome o-like features in CO difference spectra. It is suggested that electrons from NADH are distributed between branches terminated by the cytochrome o-like component, cytochrome a, and cytochrome d. With D-lactate, electrons are transported to cytochrome a, or an unidentified CN(-)-sensitive oxidase, and cytochrome d.

StereochemistryChlorpromazineMicrobiologyMixed Function OxygenasesElectron Transportchemistry.chemical_compoundOxygen ConsumptionCytochrome C1Multienzyme ComplexesGeneticsCytochrome c oxidaseNADH NADPH OxidoreductasesLactic AcidMolecular BiologyZymomonasbiologyMyxothiazolCytochrome b6f complexCytochrome bCytochrome cCytochrome dNADAerobiosisThiazolesBiochemistrychemistrySpectrophotometryCoenzyme Q – cytochrome c reductasebiology.proteinCytochromesMethacrylatesOxidation-ReductionFEMS microbiology letters
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Oxidative nuclease activity of ferromagnetically coupled μ-hydroxo-μ-propionato copper(II) complexes [Cu3(L)2(μ-OH)2(μ-propionato)2] (L=N-(pyrid-2-yl…

2008

Three doubly-bridged, trinuclear copper(II) compounds with hydroxo and carboxylato bridges, ∞ 1 [Cu 3 (L1) 2 (μ-OH) 2 (μ-propionato) 2 ] ∞ 1 [ Cu 3 ( L 1 ) 2 ( μ - OH ) 2 ( μ - propionato ) 2 ] (1) , [Cu 3 (L2) 2 (μ-OH) 2 (μ-propionato) 2 (DMF) 2 ] (2) and ∞ 1 {[Cu 3 (L3) 2 (μ-OH) 2 (μ-propionato) 2 ]} ∞ 1 { [ Cu 3 ( L 3 ) 2 ( μ - OH ) 2 ( μ - propionato ) 2 ] } [Cu 3 (L3) 2 (μ-OH) 2 (μ-propionato) 2 (DMF) 2 ]} (3) [HL1 =  N -(pyrid-2-ylmethyl)benzenesulfonylamide, HL2 =  N -(pyrid-2-ylmethyl)toluenesulfonylamide, HL3 =  N -(pyrid-2-ylmethyl)naphthalenesulfonylamide], have been synthesized and characterized. 1 is built from [Cu 3 (L1) 2 (μ-OH) 2 (μ-propionato) 2 ] clusters. Each unit contai…

StereochemistryCoordination polymerKineticschemistry.chemical_elementNaphthalenesCrystallography X-RayCleavage (embryo)Ferric CompoundsBiochemistryInorganic Chemistrychemistry.chemical_compoundOrganometallic CompoundsDNA CleavageBenzeneDeoxyribonucleasesMolecular StructureBenzeneDNACopperTolueneMagnetic susceptibilityKineticsCrystallographychemistryDrug DesignCyclic voltammetryOxidation-ReductionCopperTolueneJournal of Inorganic Biochemistry
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Multitasking Water-Soluble Synthetic G-Quartets: From Preferential RNA-Quadruplex Interaction to Biocatalytic Activity

2013

Natural G-quartets, a cyclic and coplanar array of four guanine res- idues held together through a Watson- Crick/Hoogsteen hydrogen-bond net- work, have received recently much at- tention due to their involvement in G- quadruplex DNA, an alternative higher-order DNA structure strongly suspected to play important roles in key cellular events. Besides this, syn- thetic G-quartets (SQ), which artificial- ly mimic native G-quartets, have also been widely studied for their involve- ment in nanotechnological applications (i.e., nanowires, artificial ion channels, etc.). In contrast, intramolecular syn- thetic G-quartets (iSQ), also named template-assembled synthetic G-quar- tets (TASQ), have been…

StereochemistryGuanineSupramolecular chemistryDeoxyribozyme010402 general chemistryG-QuartetsG-quadruplex01 natural sciencesCatalysischemistry.chemical_compound[CHIM]Chemical SciencesComputingMilieux_MISCELLANEOUS010405 organic chemistryOrganic ChemistryWaterRNADNAGeneral Chemistry0104 chemical sciencesG-QuadruplexeschemistryIntramolecular forceBiocatalysisHeminRNAOxidation-ReductionDNA
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Chemical model systems for cellular nitros(yl)ation reactions.

2009

S-nitros(yl)ation belongs to the redox-based posttranslational modifications of proteins but the underlying chemistry is controversial. In contrast to current concepts involving the autoxidation of nitric oxide ( • NO, nitrogen monoxide), we and others have proposed the formation of peroxynitrite (oxoperoxonitrate (1-)) as an essential intermediate. This requires low cellular fluxes of 'NO and superoxide ( • O 2 - ), for which model systems have been introduced. We here propose two new systems for nitros(yl)ation that avoid the shortcomings of previous models. Based on the thermal decomposition of 3-morpholinosydnonimine, equal fluxes of • NO and • O 2 - were generated and modulated by the …

StereochemistrySwineNitrosationIn Vitro TechniquesPhotochemistryNitric OxideBiochemistryRedoxArticlechemistry.chemical_compoundElectrophilic substitutionPhysiology (medical)Peroxynitrous AcidAnimalsAutoxidationPhenolNitrosoniumSuperoxideSuperoxide DismutaseGlutathioneIsocitrate DehydrogenasePeroxynitrous acidchemistryModels ChemicalMolsidomineNitrosationCattlePeroxynitriteFree radical biologymedicine
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Heterobimetallic complexes of cobalt(IV) porphyrin-corrole dyads. Synthesis, physicochemical properties, and X-ray structural characterization.

2005

The synthesis of a novel family of heterobinuclear cofacial biphenylene (B), anthracene (A), 9,9-dimethylxanthene (X), or dibenzofuran (O) bridged porphyrin-corrole complexes, (PCY)MClCoCl, is reported, M being either an iron(III) or manganese(III) ion. Each complex was characterized by electrochemistry, mass spectrometry, UV-vis, IR, and electron spin resonance spectroscopy. Unlike previously examined biscobalt porphyrin-corrole dyads, the cobalt ion of the corrole moiety is present in a high-valence +4 oxidation state, as proven by electrochemistry, spectroelectrochemistry, and an X-ray diffraction study of (PCB)FeClCoCl, which shows the presence of a bound Cl- anion on the cobalt corrole…

Stereochemistrychemistry.chemical_elementBiphenyleneTriclinic crystal systemPorphyrinlaw.inventionInorganic Chemistrychemistry.chemical_compoundCrystallographychemistrylawOxidation stateMoietyPhysical and Theoretical ChemistryCorroleElectron paramagnetic resonanceCobaltInorganic chemistry
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Mo-W-containing tetragonal tungsten bronzes through isomorphic substitution of molybdenum by tungsten

2010

Mixed metal oxides based in Mo(W)–Nb–V–Te with tetragonal tungsten bronze (TTB) structure have been synthesized by a hydrothermal method from aqueous solutions of the corresponding Keggin-type heteropolyacids and further heat-treatment in N2 at 700 ◦ C. The materials have been characterized by several physico-chemical techniques, i.e. XRD, Raman, FTIR, SEM-EDS, and TEM. This procedure allows controlling the chemical species to be distributed in the different interstices of the TTB skeleton, which is a key factor to regulate the catalytic properties of the final solid. In this sense, the isomorphic replacement of Mo by W results in lattice parameter and crystal morphology variation, although…

Stereochemistrychemistry.chemical_elementGeneral ChemistryTTB-bronzePartial oxidation of propeneTungstenCatalysisMo–V–Te–Nb–W–P–O mixed metal oxidesTetragonal crystal systemCrystallographyLattice constantchemistryTransition metalIsomorphic substitution of molybdenum by tungstenMolybdenumPINTURAX-ray crystallographyHydrothermal synthesisHydrothermal synthesisPartial oxidation
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Protonation and oxidation chemistry of a pentaethylcyclopentadienyl-containing molybdenum(IV) trihydride complex

2000

International audience; Compound CpEtMoCl4 (CpEt=η5-C5Et5) (1) can be transformed into CpEtMoH3(dppe) (2) and CpEtMoD3(dppe) (2-d3) [dppe=1,2-(diphenylphosphino)ethane] by reaction with LiAlX4 (X=H and D, respectively). The protonation and oxidation studies of these two compounds, in comparison with previously reported studies on (C5Me5) analogs, show important differences that may be attributed to a kinetic stabilization of the products, which is steric in nature. Protonation of 2 with HBF4 in acetonitrile affords [CpEtMoH4(dppe)]+ (3), which only slowly decomposes to [CpEtMoH2(MeCN)(dppe)]+ (4). Further protonation of the latter affords the monohydride species [Cp*MoH(dppe)(MeCN)2]2+ in t…

Steric effectsPentaethylcyclopentadienyl complexesProtonTrihydride complexesStereochemistrychemistry.chemical_elementProtonationProtonation010402 general chemistry01 natural sciencesMedicinal chemistryRedoxInorganic Chemistrychemistry.chemical_compoundOxidizing agentOxidationMaterials Chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryAcetonitrileClassical structure010405 organic chemistry0104 chemical scienceschemistryMolybdenumMolybdenum(IV) complexes
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Evidence that steric factors modulate reactivity of tautomeric iron-oxo species in stereospecific alkane C-H hydroxylation

2014

A new iron complex mediates stereospecific hydroxylation of alkyl C-H bonds with hydrogen peroxide, exhibiting excellent efficiency. Isotope labelling studies provide evidence that the relative reactivity of tautomerically related oxo-iron species responsible for the C-H hydroxylation reaction is dominated by steric factors This work has been supported by the European Union (the Erasmus Mundus program), the International Research Training Group Metal Sites in Biomolecules: Structures, Regulation and Mechanisms (www.biometals.eu), and COST Action CM1003. M.C. acknowledges ERC-29910, MINECO of Spain for CTQ2012- 37420-C02-01/BQU and CSD2010-00065, catalan DIUE (2009SGR637) and an ICREA academ…

Steric effectsStereochemistryIronrautaHydroxylationOxidacióIron compoundsCatalysisCatalysisHydroxylationchemistry.chemical_compoundStereospecificityCatàlisiCoordination ComplexesAlkanesOxidationMaterials ChemistryReactivity (chemistry)Hydrogen peroxideta116Alkylchemistry.chemical_classificationMolecular StructurekoordinaatioyhdisteetMetals and AlloysStereoisomerismcoordination compundsFerro -- CompostosGeneral ChemistryHydrogen PeroxideTautomer3. Good healthSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryCeramics and CompositesOxygenases
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