Search results for "Surfaces"

showing 10 items of 2837 documents

Comparative optical reflection and mass spectrometry analysis of thermodesorption of Langmuir-Blodgett films

1992

Abstract Thermodesorption of cadmium arachidate multilayers is studied by optical surface analysis and by mass spectrometry measurements. The optical reflection technique has been improved to discriminate signal contributions from desorption and light scattering. The scattering arises from film heterogeneities that are also observed by Nomarsky microscopy. The assessment of these heterogeneities is important to understand mass spectrometry data. Both the optical technique and mass spectrometry are sensitive to observing the multilayer phase transition at 110 °C and the desorption near 200 °C (at the heating rate applied). The mass spectrometry analysis yields detailed information on the des…

Static secondary-ion mass spectrometryScatteringChemistryMetals and AlloysAnalytical chemistrySurfaces and InterfacesThermal ionization mass spectrometryMass spectrometryLangmuir–Blodgett filmLight scatteringSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsDesorptionMicroscopyMaterials ChemistryThin Solid Films
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Fluorescence quenching by trapped charge carriers in N,N-dimethylaminobenzylidene 1,3-indandione films

2010

Effects caused by the applied voltage on the steady state and time-resolved fluorescence of vacuum evaporated N,N-dimethylaminobenzylidene 1,3-indandione films sandwiched between gold and aluminium electrodes were investigated and discussed. Fluorescence enhancement and quenching as well as the fluorescence band narrowing depending on the applied voltage have been observed. Fluorescence decay and recovery take place on a time scale of tens of seconds after voltage is switched on and off. Similar fluorescence decay also takes place after switching on the excitation light. These fluorescence changes are attributed to the exciton quenching by trapped charge carriers.

Steady stateMaterials scienceQuenching (fluorescence)13-IndandioneExcitonMetals and AlloysAnalytical chemistrySurfaces and InterfacesCondensed Matter::Mesoscopic Systems and Quantum Hall EffectPhotochemistryFluorescenceSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundchemistryMaterials ChemistryCharge carrierExcitationVoltageThin Solid Films
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Binding isotope effects as a tool for distinguishing hydrophobic and hydrophilic binding sites of HIV-1 RT.

2014

The current treatment for HIV-1 infected patients consists of a cocktail of inhibitors, in an attempt to improve the potency of the drugs by adding the possible effects of each supplied compound. In this contribution, nine different inhibitors of HIV-1 RT, one of the three key proteins responsible for the virus replication, have been selected to develop and test a computational protocol that allows getting a deep insight into the inhibitors’ binding mechanism. The interaction between the inhibitors and the protein have been quantified by computing binding free energies through FEP calculations, while a more detailed characterization of the kind of inhibitor–protein interactions is based on …

StereochemistryBinding energyHuman immunodeficiency virus (HIV)Binding energyMolecular Dynamics Simulationmedicine.disease_causeLigandsIsotopesCatalytic DomainKinetic isotope effectDrug DiscoveryMaterials ChemistrymedicinePhysical and Theoretical ChemistryBinding siteBinding isotope effectsIsotopeChemistryWaterHIV Reverse TranscriptaseSurfaces Coatings and FilmsCrystallographyViral replicationHIV-1SolventsQuantum TheoryReverse Transcriptase InhibitorsThermodynamicsFree energiesHydrophobic and Hydrophilic InteractionsProtein BindingThe journal of physical chemistry. B
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Topologically Novel Multiple Rotaxanes and Catenanes Based on Tetraurea Calix[4]arenes

2006

Calix[4]arenes bearing at their wide rim four urea residues easily form hydrogen bonded dimeric capsules. This has been used to preorganise alkenyl functions attached to these urea groups for their controlled connection via metathesis reaction. Multimacrocyclic tetraurea derivatives are thus obtained in excellent yields via heterodimers which are formed exclusively with tetratosylurea derivatives. Heterodimerisation of such bis- and tetraloop tetraureas leads analogously to multicatenanes, or to rotaxanes by stoppering. Huge macrocycles are detached from tetraloop derivatives by cleavage of the urea function.

StereochemistryChemistryCatenaneMetals and AlloysGeneral ChemistryGeneral MedicineCleavage (embryo)TetraloopCombinatorial chemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundPolymer chemistryMaterials ChemistryCeramics and CompositesUreaSalt metathesis reactionChemInform
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A heteropentanuclear oxalato-bridged [ReIV 4GdIII] complex: synthesis, crystal structure and magnetic properties

2012

The compound (NBu 4) 5[Gd III{Re IVBr 4(μ-ox)} 4(H 2O)]·H 2O (1), with intramolecular antiferromagnetic coupling, is the first Re(iv) system incorporating a 4f ion. © 2012 The Royal Society of Chemistry.

StereochemistryChemistryMetals and AlloysGeneral ChemistryCrystal structureCatalysisAntiferromagnetic couplingSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonCrystallographyIntramolecular forceMaterials ChemistryCeramics and Composites
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Chemically driven phase separation in black lipid membranes and its coupling to membrane functions

1992

Abstract We analysed the single-channel current fluctuations of gramicidin in bimolecular lipid membranes in order to demonstrate (i) the influence of protein binding to the lateral organisation of a mixed membrane, and (ii) how this couples to the function of the ionophore. Examples of phase separations induced by synthetic polyelectrolytes, as models for peripheral membrane proteins, and specific ligand-receptor interactions are presented and discussed in view of the important lateral order-function relationship in biomembranes.

StereochemistryChemistryPeripheral membrane proteinLipid microdomainMetals and AlloysSynthetic membraneBiological membraneSurfaces and InterfacesPolar membraneSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsOrientations of Proteins in Membranes databaseMembraneMaterials ChemistryBiophysicsMembrane biophysicsThin Solid Films
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Oxo-Vanadium(IV) Dihydrogen Phosphate: Preparation, Magnetic Study, and Heterogeneous Catalytic Epoxidation

2008

A layered oxo-vanadium(IV) dihydrogen phosphate, {VO(H2PO 4)2} n has been synthesized hydrothermally and characterized by several physicochemical methods. Single-crystal X-ray analysis (crystal system, tetragonal; space group, P4/ ncc; unit cell dimensions, a = b = 8.9632(4), c = 7.9768(32) A) of {VO(H2PO4) 2} n reveals that the compound has an extended two-dimensional structure. The VO2+ moieties are connected through bridging H 2PO4 (-) ions, and this type of connection propagates parallel to the crystallographic ab plane which gives rise to a layered structure. The layers are staked parallel to the crystallographic c axis with a separation between the layers of ca. 4.0 A. Magnetic suscep…

StereochemistryCrystal systemVanadiumchemistry.chemical_elementSurfaces and InterfacesAtmospheric temperature rangeCondensed Matter PhysicsMagnetic susceptibilityCatalysisTetragonal crystal systemchemistry.chemical_compoundCrystallographychemistryElectrochemistryAntiferromagnetismGeneral Materials ScienceAcetonitrileSpectroscopyLangmuir
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[FeIILSCoIIILS]2⇔ [FeIIILSCoIIHS]2 photoinduced conversion in a cyanide-bridged heterobimetallic molecular square

2010

The self-assembly of [Fe(III){B(pz)(4)}(CN)(3)](-) and [Co(II)(bik)(2)(S)(2)](2+) affords the diamagnetic cyanide-bridged [Fe(II)(LS)Co(III)(LS)](2) molecular square which is converted into the corresponding magnetic [Fe(III)(LS)Co(II)(HS)](2) species under light irradiation at relatively low temperatures.

StereochemistryCyanideMetals and AlloysLight irradiationGeneral ChemistryCatalysisSquare (algebra)Surfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundCrystallographychemistryMaterials ChemistryCeramics and CompositesDiamagnetismChemical Communications
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Synthesis and crystal structure of an unprecedented bismuth porphyrin containing ester pendant arms

2000

International audience; An easily prepared porphyrin with pendant arms is shown to form a stable complex with bismuth(III) ion; the complex is eight coordinate with a square antiprismatic coordination geometry; the solid-state structure exhibits the formation of a dimer assembled via mutual coordination of a terminal ester group.

StereochemistryDimerchemistry.chemical_elementCrystal structure010402 general chemistry01 natural sciences[ CHIM ] Chemical SciencesCatalysisBismuthIonchemistry.chemical_compoundMaterials Chemistry[CHIM]Chemical SciencesCoordination geometrySquare antiprismatic molecular geometry010405 organic chemistryChemistryMetals and AlloysGeneral ChemistryPorphyrin0104 chemical sciences3. Good healthSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyCeramics and Composites
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Mixed micelles composed of Peptides and Gadolinium complexes as tumor-specific contrast agents in MRI: a SANS study

2004

A detailed structural investigation on mixed micelle aggregates as target-specific contrast agents for magnetic resonance imaging technique has been carried out by way of small angle neutron scattering measurements. These mixed micelles are formed by two new amphiphilic molecules formed by a bioactive peptide and a claw moiety. The first molecule, C18H37CONH(AdOO)(x)-G-CCK8 (C18LxCCK8, x = 2, 5), contains an 18-carbon-atom alkylic chain bound to the C-terminal of the cholecystokinin octapeptide amide (CCK 26-33 or CCK8) and is able to bind to the overexpressed CCK receptor of some tumor cells. The second molecule, C(18)H(37)CONHLys(DTPAGlu)CONH25- (C18DTPAGlu) or its gadolinium complex [C(1…

StereochemistryGadoliniumMicelles Peptide Nanocarriers SANSContrast Media Gadolinium amide protonchemistry.chemical_elementCholecystokinin receptorMicelleSmall-angle neutron scatteringSurfaces Coatings and FilmsJchemistry.chemical_compoundchemistryAmideMaterials ChemistryMoietyMoleculeChelationddc:530Physical and Theoretical Chemistry
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