Search results for "Crystal"

showing 10 items of 22886 documents

Modeling of the N-terminal Section and the Lumenal Loop of Trimeric Light Harvesting Complex II (LHCII) by Using EPR

2015

The major light harvesting complex II (LHCII) of green plants plays a key role in the absorption of sunlight, the regulation of photosynthesis, and in preventing photodamage by excess light. The latter two functions are thought to involve the lumenal loop and the N-terminal domain. Their structure and mobility in an aqueous environment are only partially known. Electron paramagnetic resonance (EPR) has been used to measure the structure of these hydrophilic protein domains in detergent-solubilized LHCII. A new technique is introduced to prepare LHCII trimers in which only one monomer is spin-labeled. These heterogeneous trimers allow to measure intra-molecular distances within one LHCII mon…

inorganic chemicalsModels MolecularProtein ConformationProtein domainTrimerContext (language use)complex mixturesBiochemistrylaw.inventionchemistry.chemical_compoundBiopolymersProtein structurelawElectron paramagnetic resonanceMolecular BiologySuperhelixfungiElectron Spin Resonance SpectroscopyPhotosystem II Protein ComplexCell Biologyequipment and suppliesCrystallographyMonomerModels ChemicalchemistryThylakoidProtein Structure and FoldingbacteriaJournal of Biological Chemistry
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From Mono- to Poly-Substituted Frameworks: A Way of Tuning the Acidic Character of C-c-H in o-Carborane Derivatives

2009

[EN] The incorporation of iodine atoms onto the boron vertices of the o-carborane framework causes, according to spectroscopic data, a uniform increase in the acidic character of the C-c-H (C-c= cluster carbon) vertices, whereas the incorporation of methyl groups onto the boron vertices of the o-carborane framework reduces their acidity. Methyl groups when attached to boron are electron-withdrawing in boron clusters, whereas iodine atoms bonded to boron act as electron donors. This has been proven on B-methyl and B-iodinated o-carboranes with NMR spectroscopy measurements and DFT calculations of natural bond orbital (NBO) charges. which show a Cumulative buildup of positive cluster only tot…

inorganic chemicalsNatural bond orbital chargesInorganic chemistrychemistry.chemical_elementElectron010402 general chemistryIodine01 natural sciencesCatalysisQUIMICA ANALITICACluster (physics)BoronCarboranesBoron010405 organic chemistryOrganic ChemistryGeneral ChemistryNuclear magnetic resonance spectroscopy3. Good health0104 chemical sciencesCrystallographyDensity functional calculationschemistryCarboraneCarbonNatural bond orbitalIodine
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Investigation of the dynamics of bacteriorhodopsin

1990

Bacteriorhodopsin (bR) converted to the blue form by deionization has been reconstituted to the active purple membrane by addition of57Fe ions. Mossbauer spectra measured in a wide temperature range reveal Fe3+ binding places with oxygen atoms in the neighbourhood. No evidence for a well defined functional binding place of the iron has been found. On a timescale faster 100 ns the purple membrane shows increasing flexibility above 200 K. In order to analyse the influence of the lipids, a bacteriorhodopsin sample where the lipid content has been increased artificially by the incorporation of DMPC as well as a sample consisting of lipid bilayer have been investigated.

inorganic chemicalsNuclear and High Energy PhysicsbiologyChemistryBacteriorhodopsinAtmospheric temperature rangeCondensed Matter PhysicsAtomic and Molecular Physics and OpticsIonCrystallographyMembraneOxygen atomLipid contentbiology.proteinMossbauer spectraPhysical and Theoretical ChemistryLipid bilayerHyperfine Interactions
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Mössbauer and TEM studies of the perovskite system (1-y)La2/3 $$A$$ 1/3TiO3·yLaFeO3

1994

The microscopic nature of the Mossbauer phase analysis has been found as being particularly valuable in testing assumptions suggested by TEM results regarding the microdomain structure and the population of different lattice sites by iron ions in the perovskite system (1-y)La2/3\(A\)1/3TiO3·yLaFeO3 with 0.04<y < 0.25 (\(A\) is an A-site vacancy). This system was found to contain only Fe3+-phases which are stable under normal conditions, but moderate heating in vacuo causes a partial reduction of ferric ions to ferrous ions.

inorganic chemicalsNuclear and High Energy Physicseducation.field_of_studyChemistryInorganic chemistryPopulationCondensed Matter PhysicsAtomic and Molecular Physics and OpticsFerrousIonCrystallographyVacancy defectLattice (order)Mössbauer spectroscopymedicineFerricPhysical and Theoretical ChemistryPhase analysiseducationmedicine.drugHyperfine Interactions
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Crystal structure of the molecular adduct of dimethyltin(IV) chloride with N,N′-ethylenebis(salicylideneiminato) nickel(II)

1974

Abstract N,N′-Ethylenebis(salicylideneiminato)nickel(II) behaves as a neutral bidentate ligand through its oxygen atoms forming binuclear complexes with organotin(IV) chlorides. The crystal structure of the dimethyl derivative is reported.

inorganic chemicalsOrganic ChemistryInorganic chemistrychemistry.chemical_elementCrystal structureBiochemistryChlorideAdductInorganic Chemistrychemistry.chemical_compoundNickelOxygen atomchemistryPolymer chemistryMaterials ChemistrymedicinePhysical and Theoretical ChemistryDerivative (chemistry)medicine.drugJournal of Organometallic Chemistry
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Dependence of the emission properties of the germanium lone pair center on Ge doping of silica

2011

We present an experimental investigation regarding the changes induced by the Ge doping level on the emission profile of the germanium lone pair center (GLPC) in Ge doped silica. The investigated samples have been produced by the sol-gel method and by plasma-activated chemical vapor deposition and have doping levels up to 20% by weight. The recorded photoluminescence spectra show that the GLPC emission profile is the same when the Ge content is lower than ∼ 1% by weight, whereas it changes for higher doping levels. We have also performed Raman scattering measurements that show the decrease of the D1 Raman band at 490 cm( - 1) when the Ge content is higher than 1% by weight. The data suggest…

inorganic chemicalsPhotoluminescenceMaterials scienceSettore FIS/01 - Fisica SperimentaleDopingtechnology industry and agricultureAnalytical chemistrychemistry.chemical_elementGermaniumChemical vapor depositionCondensed Matter PhysicsCrystallographic defectSpectral linesymbols.namesakechemistrysymbolsGe-doped silica point defects structural propertiesddc:530General Materials ScienceLone pairRaman scatteringJournal of Physics: Condensed Matter
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Mössbauer spectroscopy on the reaction center of Rhodopseudomonas viridis

1992

Proteins called “reaction centers” (RC) can be isolated from many photosynthetic bacteria. They have one non-heme iron in a quinone acceptor region. The RC of Rhodopseudomonas viridis contains an additional tightly bound tetra-heme cytochrome c subunit. The electronic configuration of both cytochrome and the non-heme iron has been studied in the crystallized protein by Mossbauer spectroscopy at different redox potentials, pH-values, and with an addition of o-phenanthroline. At high potentials (Eh=+500mV) all heme irons are in the low spin Fe3+-state, and at low potential (Eh=−150mV) they are low spin Fe2+ with the same Mossbauer parameters for all hemes independent of pH. Redox titrations c…

inorganic chemicalsPhotosynthetic reaction centreNuclear and High Energy PhysicsbiologyCytochromeCytochrome cCondensed Matter PhysicsPhotochemistryRedoxAtomic and Molecular Physics and Opticschemistry.chemical_compoundCrystallographychemistryRedox titrationMössbauer spectroscopybiology.proteinPhotosynthetic bacteriaPhysical and Theoretical ChemistryHemeHyperfine Interactions
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Nature of activating effect of two-step polymerization of propylene

1999

The prepolymerization effect on propylene polymerization in the presence of a TiCl 3 -based catalyst, modified by di-n-buthyl ether, was studied. The influence of prepolymerization on the electron spin resonance spectra and morphology of the catalyst, as well as the properties and the morphology of both prepolymer and regular polymerization products, was investigated. The polymer morphology was evaluated through scanning electron microscopy, polymer bulk density, and particle size distribution. Some evidence of the enhancement effect of prepolymerization on the catalyst activity and stereospecificity was obtained. No influence from prepolymerization was observed on molecular weight and its …

inorganic chemicalsPolypropylenechemistry.chemical_classificationPolymers and PlasticsScanning electron microscopeorganic chemicalsGeneral ChemistryPolymerSurfaces Coatings and FilmsCatalysischemistry.chemical_compoundCrystallinitychemistryChemical engineeringPolymerizationPolymer chemistryMaterials Chemistryheterocyclic compoundsZiegler–Natta catalystPrepolymerJournal of Applied Polymer Science
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X-ray Photoelectron-spectroscopy Investigation of Pumice-supported Nickel-catalysts

1995

Pumice-supported nickel catalysts, prepared by the method of slow homogeneous precipitation with urea, were analysed by x-ray photoelectron spectroscopy (XPS). By comparison with similarly prepared silica- and alumina-supported nickel catalysts, a preferential interaction of Ni2+ with Al3+ of the support has been determined. A quantitative XPS analysis indicated large segregation of nickel to the surface. The treatment with H2 at 673 K and 1073 K produced a partial reduction of Ni+2 to Ni0. The extent of the reduction was largest at 1073 K and in this case the reduced Ni in the metallic phase was detectable by x-ray diffraction. A decrease of the Ni 2p/Si 2p intensity ratio occurring in the…

inorganic chemicalsPrecipitation (chemistry)ChemistryAnalytical chemistrySinteringchemistry.chemical_elementSurfaces and InterfacesGeneral ChemistryCondensed Matter PhysicsSurfaces Coatings and FilmsCatalysisMetalNickelTransition metalX-ray photoelectron spectroscopyvisual_artX-ray crystallographyMaterials Chemistryvisual_art.visual_art_medium
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Combined effect of noble metals (Pd, Au) and support properties on HDS activity of Co/SiO2 catalysts

2009

Abstract Cobalt-based catalysts supported on different types of SiO 2 are studied in the hydrodesulfurization of thiophene. Amorphous silica and siliceous MCM-41 and HMS, characterized by different texture and surface acidity are used as carriers. The effects due to the modification of the support by impregnation with palladium precursor and to the co-impregnation of cobalt and gold are considered. The catalysts are characterized by N 2 physisorption (BET), XRD, TPR and XPS techniques. The use as supports of the ordered mesoporous silica with higher surface area with respect to amorphous silica, produces a better dispersion of the cobalt oxides particles. Moreover, the addition of palladium…

inorganic chemicalsProcess Chemistry and TechnologyInorganic chemistrychemistry.chemical_elementMesoporous silicaCatalysisCatalysischemistry.chemical_compoundchemistryCrystalliteHydrodesulfurizationTetrahydrothiopheneCobaltCobalt oxidePalladiumApplied Catalysis A: General
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