Search results for "Faces"

showing 10 items of 3167 documents

Sorting of Enhanced Reference Raman Spectra of a Single Amino Acid Molecule

2014

In this contribution, we report the identification of the principal reference Raman spectra of a single cystein molecule. To that purpose, we design an active Surface Enhanced Raman Spectroscopy (SERS) template based on surfactant-less Chebyshev nanoparticles operating in a microfluidic platform. A principal component analysis is obtained from fluctuating spectra to sort the reference spectra of cystein. The assignment of Raman bands brings new insight into the conformation of an amino acid adsorbed onto gold nanoparticle.

chemistry.chemical_classification[PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics]Quantitative Biology::BiomoleculesSortingNanoparticleActive surfaceQuantitative Biology::GenomicsSpectral lineSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAmino acidCrystallographysymbols.namesakeGeneral EnergyAdsorptionchemistrysymbolsMoleculePhysical and Theoretical ChemistryRaman spectroscopyComputingMilieux_MISCELLANEOUSThe Journal of Physical Chemistry C
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A giant hybrid organic-inorganic octahedron from a narrow rim carboxylate calixarene.

2020

Here we discovered an unprecedented giant octahedral coordination compound bearing 16 Zn2+, 12 Na+, 8 O2-, 4 OH-, 13 H2O and 6 L4- ligands [L4- = fully deprotonated tetra(carboxymethoxy)calix[4]arene]. Its structure was elucidated by single-crystal X-ray diffraction, wavelength-dispersive X-ray spectroscopy and MALDI-TOF mass spectrometry. This compound, Zn8Na6L6⊃Zn8Na6O8(OH)4(H2O)13 (external⊃internal), has eight tetrahedral zinc ions forming the coordination vertices of an outermost cube where carboxylate groups from the sodium calixarenes are anchored. Its core consists of eight Zn2+, six Na+, eight O2-, and four OH- distributed over three layers, besides thirteen coordinated H2O molecul…

chemistry.chemical_classificationbiologySodiumMetals and Alloyschemistry.chemical_elementGeneral Chemistrybiology.organism_classificationCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCoordination complexQUÍMICA INORGÂNICACrystallographychemistry.chemical_compoundDeprotonationchemistryOctahedronCalixareneMaterials ChemistryCeramics and CompositesTetraMoleculeCarboxylateChemical communications (Cambridge, England)
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Stability of the functional NLO polymers–optically induced depoling of the DMABI molecules in sPMMA matrix

2008

Abstract Low polar order (PO) stability is the major problem of the polymer materials for nonlinear optical (NLO) applications. In this contribution we will show the results of PO stability investigations in the corona poled 3 wt.% DMABI + sPMMA guest–host system. Influence of the poling temperature on the building and stability of the polar order in the system will be presented. To characterize the stability, PO destruction has been caused by high intensity light. Polar order stability characteristics were obtained from the sample second harmonic generation intensity (SHI) time decays. We have found that the decay signal is the best fit to the sum of two exponentials. Several physical mode…

chemistry.chemical_classificationbusiness.industryChemistryKineticsPolingMetals and AlloysSecond-harmonic generationNonlinear opticsSurfaces and InterfacesPolymerCorona polingSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsOpticsChemical physicsMaterials ChemistryPolarMoleculebusinessThin Solid Films
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Polymers films with indandione derivatives as alternatives to azobenzene polymers for optical patterning

2008

Surface relief gratings (SRGs) on organic thin films are studied extensively for both scientific interest and in relevance to the applications. Among the chromophores being used the azobenzenes showed the best performance, but the use of alternative photo-sensitive groups provides better general understanding of the phenomena. A thermodynamic theory and molecular dynamics simulations of photoinduced effects are discussed. In this study we use indandione derivatives, known as promising materials for photonics applications, as an alternative to the azobenzenes. We consider their photoreactions when incorporated into a polymer film. One of interesting features is the spectral dependence of the…

chemistry.chemical_classificationbusiness.industryMetals and AlloysNanotechnologySurfaces and InterfacesPolymerChromophoreSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMolecular dynamicschemistry.chemical_compoundOpticsAzobenzenechemistryMaterials ChemistryNear-field scanning optical microscopePhotonicsThin filmbusinessDiffraction gratingThin Solid Films
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Liquid crystal polymers (LCP) as processing aids and reinforcing agents. A study of nylon 6/LCP blends

1989

Influence de petites quantites d'un copolyesteramide thermotropique sur les proprietes mecaniques et la mise en œuvre du polyamide 6

chemistry.chemical_classificationchemistry.chemical_compoundNylon 6Materials sciencePolymers and PlasticschemistryLiquid crystalMaterials ChemistryGeneral ChemistryPolymerComposite materialSurfaces Coatings and FilmsJournal of Applied Polymer Science
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A Novel Zeolite-Induced Population of a Planar Viologen Conformation. New Viologen Charge Transfer Complexes and Alkene/Viologen/Zeolite Arrays

2004

A rare example of a novel zeolite-induced conformational change and a mechanism for this process are suggested in order to rationalize an unexpected spontaneous intrazeolite reduction observed during preparation of a new viologen (MQ2+)-doped zeolite (NaY). In addition, the formations of six new alkene/viologen/ zeolite charge transfer (CT) arrays using NaMQY and the previously reported NaMVY are also reported. The binding constants between MQ2+ and MV2+ and 2,3-dimethyl-2-butene (TME) were determined using the Benesi-Hildebrand approach, and the stabilities of these CT complexes are compared to their intrazeolite analogue.

chemistry.chemical_classificationeducation.field_of_studyConformational changeChemistryAlkenePopulationViologenCharge (physics)Settore CHIM/06 - Chimica OrganicaPhotochemistrySurfaces Coatings and FilmsPlanarMaterials ChemistrymedicinePhysical and Theoretical ChemistryeducationZeolitemedicine.drugZeolites Binding constants Electrochromic display devices Oxygenation
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Stratification in Drying Polymer–Polymer and Colloid–Polymer Mixtures

2017

Drying polymer-polymer and colloid-polymer mixtures were studied using Langevin dynamics computer simulations. Polymer-polymer mixtures vertically stratified into layers, with the shorter polymers enriched near the drying interface and the longer polymers pushed down toward the substrate. Colloid-polymer mixtures stratified into a polymer-on-top structure when the polymer radius of gyration was comparable to or smaller than the colloid diameter, and a colloid-on-top structure otherwise. We also developed a theoretical model for the drying mixtures based on dynamical density functional theory, which gave excellent quantitative agreement with the simulations for the polymer-polymer mixtures a…

chemistry.chemical_classificationendocrine systemdigestive oral and skin physiologyStratification (water)Thermodynamics02 engineering and technologySurfaces and InterfacesPolymer010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physicscomplex mixtures01 natural sciences0104 chemical sciencesbody regionsColloidchemistryElectrochemistryRadius of gyrationOrganic chemistryGeneral Materials ScienceDensity functional theory0210 nano-technologyLangevin dynamicsSpectroscopyLangmuir
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Structural Investigation of Water/Lecithin/Cyclohexane Microemulsions by FT-IR Spectroscopy

1995

Abstract FT-IR spectra of water/lecithin/deuterated cyclohexane microemulsions as a function of water/lecithin molar ratio R ( R = [water]/[lecithin]) at various volume fractions ( O ) of the micellar phase have been recorded at 25°C. After elimination of the small spectral contributions due to deuterated cyclohexane and normalization, the shape of the C–H stretching band due to lecithin has been found dependent upon R and O whereas that of the O–H stretching band has been found dependent only upon R . The change in shape of the C–H band was interpreted in terms of a modification of the lecithin alkyl chain packing order. The analysis of the O–H band provides evidence that the hydroxylic gr…

chemistry.chemical_classificationfood.ingredientCyclohexaneHydrogen bondChemistryLecithinSpectral lineSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundColloid and Surface ChemistryfoodDeuteriumPhase (matter)Organic chemistryPhysical chemistryMicroemulsionAlkylJournal of Colloid and Interface Science
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Photooxidation and Stabilization of Photooxidized Polyethylene and of its Monopolymer Blends

2003

The increasing use of products from recycled polymers, or from blends with recycled polymers exposed to the outdoors, implies the need for good weathering resistance. This is particularly important when the recycled material comes, in turn, from products exposed during their lifetime to the sun. In this case the presence of C=O groups in the macromolecular chains strongly increases the photooxidative degradation kinetics of these secondary materials. In this work the change of the photooxidative degradation of blends of virgin and photooxidized polyethylene was evaluated as a function of the C=O content present in the material. As expected, the presence of the C=O groups strongly increases …

chemistry.chemical_classificationpolyethylene (PE)Materials sciencePolymers and PlasticsphotooxidationKineticsGeneral ChemistryPolymerPolyethylenemechanical propertiesphoto-oxidationSurfaces Coatings and Filmsstabilizationchemistry.chemical_compoundchemistryChemical engineeringpolymeric filmPolymer chemistryMaterials ChemistryPhotooxidative degradationPolymer blendHALSElongationMacromoleculeStabilizer (chemistry)
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Structural characterization of U(VI) surface complexes on kaolinite in the presence of humic acid using EXAFS spectroscopy.

2007

To determine the influence of humic acid (HA), pH, and presence of atmospheric CO2 on the sorption of U(VI) onto kaolinite, the structure of the surface complexes was studied by U L III-edge extended X-ray absorption fine structure (EXAFS) spectroscopy. The best fits to the experimental EXAFS data were obtained by including two uranium coordination shells with two axial (O ax) and five equatorial (O eq) oxygen atoms at 1.77+/-0.02 and 2.34+/-0.02 A, respectively, and two coordination shells with one Al/Si atom each at 3.1 and 3.3 A. As in the case of the binary system U(VI)-kaolinite, uranium forms inner-sphere surface complexes by edge sharing with aluminum octahedra and/or silicon tetrahe…

chemistry.chemical_classificationsorptionkaoliniteExtended X-ray absorption fine structureAnalytical chemistrySorptionhumic acidSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialsEXAFSColloid and Surface ChemistryAdsorptionchemistryX-ray photoelectron spectroscopyuranium(VI)XPSHumic acidKaoliniteAbsorption (chemistry)surface complexesSpectroscopyJournal of colloid and interface science
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