Search results for "Isotropy"

showing 10 items of 1099 documents

Anisotropic Stick-slip friction of highly oriented thin films of poly(tetrafluoroethylene) at the molecular level

1996

Lateral force microscopy (LFM) studies of poly(tetrafluoroethylene) (PTFE) films with molecular resolution are reported. Thin PTFE layers with a high degree of orientation were obtained by pressing and sliding a block of polymer on a clean, heated muscovite mica substrate. LFM nanographs obtained on these films by scanning at directions between ca. 40 and 90° with respect to the film orientation direction, i.e. with respect to the direction of the polymer chains, showed a “stick-slip” type frictional motion of the LFM probe tip at the molecular level. The friction force observed at constant load decreased with decreasing scan angles. Chain-chain packing distances obtained by LFM and contact…

chemistry.chemical_classificationPressingMaterials scienceMechanical EngineeringMuscoviteNanotechnologySurfaces and InterfacesPolymerSlip (materials science)engineering.materialSurfaces Coatings and Filmschemistry.chemical_compoundchemistryMechanics of MaterialsMicroscopyengineeringTetrafluoroethyleneComposite materialThin filmAnisotropyTribology letters
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Elastic properties of polymer interfaces: Aggregation of pure diblock, mixed diblock, and triblock copolymers

2002

Block copolymers adsorbing to an interface between two immiscible homopolymers modify the elastic constants of this interface. Within self-consistent field calculations for Gaussian chains, we determine how the bending constants vary in dependence on the block copolymer concentration and architecture. Four phenomena are discussed. (i) When a tricritical or isotropic Lifshitz critical point is approached in a ternary mixture by varying the concentration of diblock copolymers or changing temperature, the elastic constants vanish. We determine the corresponding power laws, and show that the de Gennes--Taupin criterium for the stability of lamellar phases against undulations and the Ginzburg-La…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceIsotropyThermodynamicsFlexural rigidityBendingPolymerJCondensed Matter::Soft Condensed MatterchemistryCritical point (thermodynamics)Copolymerddc:530Lamellar structureTernary operationPhysical Review E
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Rheological behaviour, filmability and mechanical properties of biodegradable polymer films

2014

The rheological properties in shear flow and non isothermal elongational flow of two biodegradable polymers, belonging to two different classes of materials, have been measured and compared with those of a film blowing grade high density polyethylene in order to assess the filmability of these polymers. The mechanical properties of isotropic and anisotropic samples have been also reported.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceIsotropytechnology industry and agriculturePolymerBiodegradable polymerIsothermal processCondensed Matter::Soft Condensed MatterRheologychemistryHigh-density polyethyleneComposite materialAnisotropyShear flowbiodegradable filmAIP Conference Proceedings
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Near Isotropic D4d Spin Qubits as Nodes of a Gd(III)-Based Metal-Organic Framework

2021

Embedding coherent spin motifs in reproducible molecular building blocks is a promising pathway for the realization of quantum technologies. Three-dimensional (3D) MOFs are a versatile platform for the rational design of extended structures employing coordination chemistry. Here, we report the synthesis and characterization of a gadolinium(III)-based MOF, [Gd(bipyNO)4](TfO)3·xMeOH (bipyNO = bipyridine,N,N′-dioxide; TfO = triflate; and MeOH = methanol) (quMOF-1), which presents a unique coordination geometry that leads to a tiny magnetic anisotropy (in terms of D, an equivalent zero-field splitting would be achieved by D = 0.006 cm–1) even compared with regular Gd(III) complexes. Pulsed elec…

chemistry.chemical_classificationRabi cycle010405 organic chemistryChemistryPulsed EPRQuímica010402 general chemistry01 natural sciencesMolecular physicsArticle0104 chemical sciences3. Good healthCoordination complexInorganic ChemistryMagnetic anisotropyBipyridinechemistry.chemical_compoundQubitPhysical and Theoretical ChemistrySpin (physics)Coordination geometry
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Measurement of the strain-optic coefficients of PMMA from 800 to 2000 nm

2020

The strain-optic coefficients of PMMA are measured in a broad wavelength range from 800 to 2000 nm. The sensitivity of the azimuthal whispering gallery mode resonances to the strain is exploited to measure the strain-optic coefficients of PMMA micro-rods. The technique is based on measuring the wavelength shift of the resonances of both polarizations states, the TE and TM, when an axial strain is applied to the polymer rods. This method enables the determination of the strain-optic coefficients of the material in a broad wavelength range. In particular, in the near-infrared range, the PMMA exhibits negligible dispersion and anisotropy, and the strain-optic coefficients show constant values …

chemistry.chemical_classificationRange (particle radiation)Materials scienceUNESCO::FÍSICAPolymerMolecular physicsPMMAAtomic and Molecular Physics and OpticsRodElectronic Optical and Magnetic MaterialsAzimuthchemistryFiber Bragg grating:FÍSICA [UNESCO]Dispersion (optics)Electrical and Electronic EngineeringWhispering-gallery wavewhispering gallery modesAnisotropystrain-optic coefficients
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Embryotoxicity studies of tri-n-butyltin(IV) complexes of 5-[(E)-2-(aryl)-1-diazenyl]-2-hydroxybenzoic acid and 2-[(E)-2-(3-formyl-4-hydroxyphenyl)-1…

2005

The toxicity studies of free 5-[(E)-2-(aryl)-1-diazenyll-2-hydroxybenzoic acid and 2-[(E)-2-(3-formyl-4-hydroxyphenyl)-1-diazenyllbenzoic acid and their tri-n-butyltin(IV) complexes were evaluated by using sea urchin early developmental stages as recommended model organisms for toxicity tests. The novel complexes, as the parent tri-n-butyltin(IV) chloride (TBTCl), caused mitosis block and induced high embryonic mortality in sea urchin. Copyright (c) 2005 John Wiley & Sons, Ltd.

chemistry.chemical_classificationSPECTRUMAzo compoundbiologyStereochemistryCarboxylic acidArylSMALL-SCALE ANISOTROPYGeneral ChemistryPhenolic acidbiology.organism_classificationParacentrotus lividusENERGY COSMIC-RAYSInorganic Chemistrychemistry.chemical_compoundchemistrybiology.animalSphaerechinus granularisSea urchinBenzoic acidApplied Organometallic Chemistry
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Liquid-crystalline ordering as a concept in materials science: from semiconductors to stimuli-responsive devices.

2013

While the unique optical properties of liquid crystals (LCs) are already well exploited for flat-panel displays, their intrinsic ability to self-organize into ordered mesophases, which are intermediate states between crystal and liquid, gives rise to a broad variety of additional applications. The high degree of molecular order, the possibility for large scale orientation, and the structural motif of the aromatic subunits recommend liquid-crystalline materials as organic semiconductors, which are solvent-processable and can easily be deposited on a substrate. The anisotropy of liquid crystals can further cause a stimuli-responsive macroscopic shape change of cross-linked polymer networks, w…

chemistry.chemical_classificationSolid-state chemistryMaterials scienceNanotechnologyGeneral ChemistryPolymerCatalysisCrystalOrganic semiconductorchemistryLiquid crystalArtificial muscleSelf-assemblyAnisotropyAngewandte Chemie (International ed. in English)
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Anisotropic Effect after Stretching of the Spin-Crossover Compound [Fe(II)(2,6-bis-(benzimidazol-2′-yl)pyridine)2] (C1O4)2 in Polyvinylalcohol Polyme…

1999

Abstract [Fe(II)(2,6-bis-(benzimidazol-2′-yl)-pyridine)2](C1O4)2 diffused into a poly(vinyl)alcohol polymer matrix, exhibits an thermally induced spin-crossover. After stretching the matrix, the compound orients itself in the matrix. Polarised UV/VIS spectra measured parallel and perpendicular to the stretching direction allowed to calculate the distortion of the molecule in the matrix by means of semi-empirical PPP SCF-CI calculations.

chemistry.chemical_classificationSpin statesStereochemistryPolymerCondensed Matter Physicschemistry.chemical_compoundCrystallographyMatrix (mathematics)chemistrySpin crossoverPyridinePerpendicularMoleculePhysics::Chemical PhysicsAnisotropyMolecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals
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Light Induced Modifications of Langmuir-Blodgett-Multilayer Assemblies Containing Amphotropic Azocopolymer

1994

Abstract Photochromic LB-multilayers of amphotropic copolymers having rod-like azobenzene moieties as side groups which exhibit thermotropic liquid crystalline behaviour in the bulk have been characterized by UV-VIS spectroscopy as well as by angular dependent and energy dispersive SAXS. Upon irradiation with UV-light the initial optical in-plane anisotropy and the vertical layered structure of LB-films can be destroyed. A new layered structure can be rebuilt on irradiation with visible light or by annealing. Using linearly polarized light for the irradiation an optical anisotropy (POA) has been induced or reversibly modified by a photoselection process.

chemistry.chemical_compoundPhotochromismAzobenzeneChemistryLiquid crystalPolymer chemistryIrradiationCondensed Matter PhysicsAnisotropyPhotochemistryThermotropic crystalLangmuir–Blodgett filmVisible spectrumMolecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals
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ChemInform Abstract: Observation of New Oscillatory Phenomena During the Electrochemical Anodization of Silicon.

2010

This paper reports the observation of large undamped voltage oscillations during the anodic polarization of silicon in electrol yte containing a combination of acids. One of them stimulates oxide growth and the other its chemical dissolution (in the present c ase, (0.01-0.1 M H3PO4) + (0.001- 0.01 M HF). This temporal patterning of the anodization process is shown to be due to the formation of a thin (50-90 nm) oxide layer at the sample surface and its subsequent lifting-off. The mechanism of oxide detachment i s thought to be an isotropic growth of micropores at the oxide/silicon interface triggered on by changes of electrochemical condi tions there.

chemistry.chemical_compoundSiliconchemistryChemical engineeringAnodizingIsotropyOxidechemistry.chemical_elementGeneral MedicinePolarization (electrochemistry)ElectrochemistryLayer (electronics)AnodeChemInform
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