Search results for "Mono"

showing 10 items of 6843 documents

Structural evolution of Pt/ceria-zirconia TWC catalysts during the oxidation of carbon monoxide

2004

The structural evolution of two Pt/ceria–zirconia catalysts, characterized by different amounts of supported Pt, was monitored by in situ X-ray diffraction during the anaerobic oxidation of CO at different temperatures. In a first phase, oxygen coming from the surface layers of the ceria–zirconia mixed oxide is consumed and no structural variation of the support is observed. After this induction time, bulk reduction of Pt/ceria–zirconia takes place as a step-like process, while the CO2 production continues at a nearly constant rate. This behavior is totally different from that of the metal-free support in similar reaction conditions, that show a gradual bulk reduction. In repeated oxidation…

chemistry.chemical_classificationInorganic chemistrychemistry.chemical_elementCondensed Matter PhysicsChemical reactionElectronic Optical and Magnetic MaterialsCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryTransition metalMaterials ChemistryCeramics and CompositesMixed oxideCubic zirconiaCompounds of carbonPhysical and Theoretical ChemistryPlatinumCarbon monoxide
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Controllable membrane remodeling by a modified fragment of the apoptotic protein Bax.

2021

Intrinsic apoptosis is orchestrated by a group of proteins that mediate the coordinated disruption of mitochondrial membranes. Bax is a multi-domain protein that, upon activation, disrupts the integrity of the mitochondrial outer membrane by forming pores. We strategically introduced glutamic acids into a short sequence of the Bax protein that constitutively creates membrane pores. The resulting BaxE5 peptide efficiently permeabilizes membranes at acidic pH, showing low permeabilization at neutral pH. Atomic force microscopy (AFM) imaging showed that at acidic pH BaxE5 established several membrane remodeling modalities that progressively disturbed the integrity of the lipid bilayer. The AFM…

chemistry.chemical_classificationIntrinsic apoptosisLipid BilayersPeptideApoptosis02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyMicroscopy Atomic Force01 natural sciencesArticle0104 chemical sciencesMembranechemistryApoptosisMonolayerMitochondrial MembranesBiophysicsPhysical and Theoretical Chemistry0210 nano-technologyDigestionBacterial outer membraneLipid bilayerbcl-2-Associated X ProteinFaraday discussions
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An Unusual Geometry of Five-Coordinate Copper(II): The Structure of Cu(terpy)I2 and Spectroscopic Investigations of Complexes Cu(terpy)X2 (X: I, NCS)

1991

The structure of the compound Cu(terpy)I2 (terpy 2,2′: 6′, 2″ terpyridine) was determined at room temperature. It is monoclinic, space group I2/c with a = 13.689(3), b = 9.510(2), c = 11.605(3) Å, β = 97.59(4)° and Ζ = 4. The copper(II) ions are five-coordinated by the three nitrogen atoms from the terpy ligand and the two iodine atoms. The CuN3I2 polyhedron exhibits the same unusual “reverse” geometry as is observed for Cu(terpy)(NCS)2. Single crystal EPR measurements of the iodide and the isothio-cyanate complexes confirmed the structural results, excluding the possibility of a dynamically averaged geometry.

chemistry.chemical_classificationIodidechemistry.chemical_elementGeometryGeneral ChemistryCrystal structureCopperlaw.inventionchemistry.chemical_compoundchemistrylawX-ray crystallographyTerpyridineElectron paramagnetic resonanceSingle crystalMonoclinic crystal systemZeitschrift für Naturforschung B
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Structural dissection of the multidomain kininogens. Fine mapping of the target epitopes of antibodies interfering with their functional properties.

1993

Kininogens, the large precursor molecules of the vasoactive kinin peptides, are prototypic multidomain proteins serving numerous functions. To investigate their structure-function relationships, we have raised a panel of monoclonal antibodies against human H-kininogen and L-kininogen and fragments thereof and characterized them with respect to their target epitopes. Of 35 antibodies, 12 were directed to the amino-terminal domains (D1 to D3) of cystatin-like structure, 3 recognized domain D4 bearing the kinin segment, 17 bound to the carboxyl-terminal domains of H-kininogen (D5H and D6H), and 3 bound to the carboxyl-terminal domain D5L of L-kininogen. At least 14 distinct epitopes spread ove…

chemistry.chemical_classificationKininogenCofactor bindingmedicine.drug_classPeptideCell BiologyBiologyKininMonoclonal antibodyBiochemistryMolecular biologyEpitopelaw.inventionchemistryBiochemistrylawbiology.proteinRecombinant DNAmedicineAntibodyMolecular Biologycirculatory and respiratory physiologyJournal of Biological Chemistry
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Properties of Hydrophobic Polymer Melts Tethered to the Water Surface As Determined with in Situ X-ray Reflectivity

1997

Insoluble monolayers of hydrophobic polymers with low glass transition temperature (perfluoropolyethers, polyisoprenes) and a single ionic head group (carboxylic acid, sulfonate) have been characterized at the air/water interface via X-ray reflectivity measurements. The films are considerably thicker (30−420 A) than conventional Langmuir monolayers of low molecular weight substances or polymers with surface active repeat units. The thickness is inversely proportional to the area per head group and is in accordance with a model assuming a solvent-free hydrophobic layer of the same density as the bulk material.

chemistry.chemical_classificationLangmuirPolymers and PlasticsOrganic ChemistryIonic bondingPolymerInorganic ChemistryX-ray reflectivityEnd-groupchemistry.chemical_compoundSulfonatechemistryChemical engineeringPolymer chemistryMonolayerMaterials ChemistryGlass transitionMacromolecules
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An Easy Way Towardɛ-Caprolactone Macromonomers by Microwave Irradiation Using Early Lanthanide Halides as Catalysts

2002

Poly(e-caprolactone) macromonomers were synthesized under microwave irradiation from commercial caprolactone, using commercial hydrated lanthanide halides as catalysts. The molecular weight of the polymers was in the range 3 000–5 000. Higher molecular weights (5 000–20 000) and lower polydispersity indices were obtained with THF adducts of the lanthanide halides as catalysts and also by applying longer reaction times or using diethylene glycol as a coupling reagent.

chemistry.chemical_classificationLanthanideMaterials sciencePolymers and PlasticsOrganic ChemistryDispersityDiethylene glycolHalidePolymerMacromonomerRing-opening polymerizationchemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryCaprolactoneMacromolecular Rapid Communications
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Synthesis and X-Ray Single Crystal Structure of Two New Copper Complexes with the Redox Active Ligand 1,10-Phenanthroline-5,6-dione

2005

The synthesis and the crystal structures of the complexes [Cu(LI)2](ClO4) (1) and [Cu(LI)(CH3CN)2(ClO4)2] (2) are reported. 1 crystallizes in the monoclinic space group C2/c with the unit cell dimensions a = 13.169(4), b = 12.289(3), c = 14.732(3) A, β = 109.03(2)° and Z = 4. Copper(I) is coordinated to four N atoms of the two 1,10-Phenanthroline-5,6-dione (LI) ligands with a two-fold axis passing between the ligands. The copper(II) compound 2 crystallizes in the orthorhombic space group Pbn21 with unit cell dimensions of a = 7.498(5), b = 23.492(7), c = 12.363(4) A and Z = 4. Copper(II) coordination can be described as a distorted octahedron with the N donor atoms of one LI ligand and of t…

chemistry.chemical_classificationLigandPhenanthrolinechemistry.chemical_elementCrystal structureCopperCoordination complexInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryOctahedronOrthorhombic crystal systemMonoclinic crystal systemZeitschrift für anorganische und allgemeine Chemie
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Metal ion affinity-based biomolecular recognition and conjugation inside synthetic polymer nanopores modified with iron-terpyridine complexes.

2011

Here we demonstrate a novel biosensing platform for the detection of lactoferrin (LFN) via metal-organic frameworks, in which the metal ions have accessible free coordination sites for binding, inside the single conical nanopores fabricated in polymeric membrane. First, monolayer of amine-terminated terpyridine (metal-chelating ligand) is covalently immobilized on the inner walls of the nanopore via carbodiimide coupling chemistry. Second, iron-terpyridine (iron-terPy) complexes are obtained by treating the terpyridine modified-nanopores with ferrous sulfate solution. The immobilized iron-terPy complexes can be used as recognition elements to fabricate biosensing nanodevice. The working pri…

chemistry.chemical_classificationLigandPolymersPyridinesSurface PropertiesMetal ions in aqueous solutionIronInorganic chemistrytechnology industry and agricultureGeneral ChemistryBiosensing TechniquesBiochemistryCombinatorial chemistryCatalysisNanoporechemistry.chemical_compoundLactoferrinNanoporesColloid and Surface ChemistrychemistryMonolayerNon-covalent interactionsTerpyridineNanodeviceBiosensorJournal of the American Chemical Society
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High Pressure Solubility Data of the System Limonene + Linalool + CO2

2001

The feasibility of deterpenating orange peel oil with supercritical CO2 depends on relevant vapor−liquid equilibrium data because the selectivity of this solvent for limonene and linalool (the two key components of the oil) is of crucial importance. In this work the solubility data for the CO2 + limonene + linalool ternary system were measured at (318.2 and 328.2) K. The range of pressures covered was from (70 to 110) bar. Two different mixtures of limonene + linalool were used:  a 40 mass % limonene + 60 mass % linalool mixture and a 60 mass % limonene + 40 mass % linalool mixture. To correlate the obtained results, two equations of state were successfully used (Peng−Robinson (PR) and Soav…

chemistry.chemical_classificationLimoneneTernary numeral systemChemistryGeneral Chemical EngineeringMonoterpeneGeneral ChemistrySupercritical fluidSolventchemistry.chemical_compoundHydrocarbonLinaloolOrganic chemistrySolubilityJournal of Chemical & Engineering Data
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How to Bridge the Gap Between Membrane Biology and Polymer Science

1986

Can polymer chemists contribute to the understanding or even mimicking of cell membrane functions and cell-cell interactions? Fascinated by the specificity and efficiency of, for example, the destruction of tumor cells by lymphocytes (1) and having in mind what biochemical analyses tell us about membrane composition, we may try to “synthesize” membrane and cell models. The commonly used model systems, such as planar lipid monolayers at the gas-water interface, bimolecular lipid membranes and spherical liposomes, are much less stable than natural membrane systems (Figure 1).

chemistry.chemical_classificationLiposomeMaterials scienceCellMembrane biologyPolymerMembrane compositionCell membranemedicine.anatomical_structureMembranechemistryMonolayermedicineBiophysics
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