Search results for "Optical"

showing 10 items of 7671 documents

Flexible Synthesis of Planar Chiral Azoninones and Optically Active Indolizidinones

2014

The flexible synthesis of defined substituted optically active indolizidinones starting from chiral pool (S)-proline and trans 4-hydroxy-(S)-proline is described. Several defined 2-vinylpyrrolidines were generated in short sequences. The aza-Claisen rearrangement using chloro and phenylketene equivalents delivered nine-membered-ring lactams with up to three stereogenic centres and pS-arranged E olefins. Depending on the substitution pattern, certain azoninones had a flexible conformation and showed pS/pR double-bond flipping. Treatment of the unsaturated lactams with the soft electrophile iodine induced diastereoselective transannular ring contractions. Here, the planar chiral arrangement o…

chemistry.chemical_classificationPlanarDouble bondchemistryStereochemistryOrganic ChemistryElectrophileMoleculePhysical and Theoretical ChemistrySigmatropic reactionOptically activeRing (chemistry)StereocenterEuropean Journal of Organic Chemistry
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Pollutant Adsorbtion and Detection: Methyl-Substituted α-Cyclodextrin as Affinity Material for Storage, Separation, and Detection of Trichlorofluorom…

2018

The cover image depicts the hazard caused by chlorofluorocarbons such as CFC‐11, which are used, for example, as blowing agents for polyurethane foams, and the protective effect of the oligosaccharide, hexakis‐(2,3,6‐tri‐O‐methyl)‐α‐cyclodextrin, which is capable of binding CFC‐11 by supramolecular complexation and thus protecting the stratospheric ozone layer from the harmful trichlorofluoromethane. Further details can be found in article number 1800057 by Ralf Hellmann, Siegfried R. Waldvogel, and co‐workers.

chemistry.chemical_classificationPollutantoptical sensorsCyclodextrinTrichlorofluoromethaneGlobal challengesCFC‐11Supramolecular chemistrysupramolecular chemistrychemistry.chemical_compoundAdsorptioncyclodextrinchemistryCover PictureOrganic chemistrytrichlorofluoromethaneGlobal Challenges
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Citric Acid Based Carbon Dots with Amine Type Stabilizers: pH-Specific Luminescence and Quantum Yield Characteristics

2020

We report the synthesis and spectroscopic characteristics of two different sets of carbon dots (CDs) formed by hydrothermal reaction between citric acid and polyethylenimine (PEI) or 2,3-diaminopyridine (DAP). Although the formation of amide-based species and the presence of citrazinic acid type derivates assumed to be responsible for a blue emission is confirmed for both CDs by elemental analysis, infrared spectroscopy, and mass spectrometry, a higher abundance of sp2-hybridized nitrogen is observed for DAP-based CDs, which causes a red-shift of the n-π* absorption band relative to the one of PEI-based CDs. These CD systems possess high photoluminescence quantum yields (QY) of ∼40% and ∼48…

chemistry.chemical_classificationPolyethylenimineChemistryLigandQuantum yieldchemistry.chemical_element02 engineering and technologyPolymer010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundGeneral Energyddc:530Amine gas treatingPhysical and Theoretical Chemistry0210 nano-technologyLuminescenceCitric acidCarbonNuclear chemistryThe Journal of Physical Chemistry C
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On the handedness of helical aggregates of C3 tricarboxamides: a multichiroptical characterization

2015

A complete chiroptical characterization of the supramolecular polymers formed by tricarboxamides (S)-1 and (R)-1 is performed using ECD, VCD and CPL dichroic techniques. The helical aggregates show an intense CPL signal and their absolute P- or M-configuration is assigned with the help of theoretical calculations.

chemistry.chemical_classificationPolymersMetals and AlloysStereoisomerismGeneral ChemistryPolymerDichroic glassAmidesCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCharacterization (materials science)Supramolecular polymersCrystallographychemistryMaterials ChemistryCeramics and CompositesChemical Communications
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Electronic Perspective on the Electrochemistry of Prussian Blue Films

2009

The derivative of the voltabsommetric scans, together with previous nano-electrogravimetric and X-ray diffraction results, allow different electrochemical processes to be distinguished during the Prussian blue (PB) voltammetric scan. Potassium, proton, and hydrated proton counterions involved in PB electrochemistry are related here to the electrochemical reactions of specific Fe sites. Potassium counterions show two different sites for their insertion: one located in the crystalline framework and another in ferrocyanide vacancies. From the monitoring of electroactive Fe sites, the covalent-exchange model is suggested as one of the first approaches to explain the origin of the PB magnetic or…

chemistry.chemical_classificationPrussian blueProtonIon exchangeRenewable Energy Sustainability and the EnvironmentPotassiumInorganic chemistrychemistry.chemical_elementCondensed Matter PhysicsElectrochemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundchemistryX-ray crystallographyMaterials ChemistryElectrochemistryCounterionFerrocyanideJournal of The Electrochemical Society
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Usefulness of F(dm/dQ) Function for Elucidating the Ions Role in PB Films

2007

The conversion process of "insoluble" prussian blue (PB) films into the "soluble" structure has been followed by the simultaneous measurement of current and mass changes during voltammetric experiments and focusing on the possibilities of the use of the instantaneous mass/electrical charge ratio at each potential. A similar procedure was used for the analysis of the mechanism of reduction of PB films to the Everitt's salt form and to follow the partial dissolution of iron species during the oxidation to the prussian yellow form. The possibility of covering PB films by Nafion membranes, which make difficult the transport of anions through it, allows us to discern the role of anions in the so…

chemistry.chemical_classificationPrussian blueRenewable Energy Sustainability and the EnvironmentAnalytical chemistrySalt (chemistry)Nafion membraneCondensed Matter PhysicsElectric chargeSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonchemistry.chemical_compoundchemistrySolubilizationMaterials ChemistryElectrochemistryDissolutionJournal of The Electrochemical Society
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Insight in NLO Polymer Material Behavior from Langevin Dynamic Modeling of Chromophore Poling

2011

Calculation of chromophore polar order, i.e. the polarization of nonlinear optically (NLO) active polymers poled by external field, is challenging. One possible solution is to reproduce the orientation polarization of chromophores under external field using Langevin dynamics (LD) molecular modeling. The present work investigates the influence of chromophore dipole moment, density and field extent on NLO efficiency and polarization/relaxation dynamics. Results of simulations convince us, that the method is applicable for modeling real NLO polymers. In the spotlight of this investigation we would like to describe a NLO polymer as a “ferrofluid” where chromophores are active particles or elect…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesFerrofluidMaterials sciencebusiness.industryPolingPolymerChromophoreCondensed Matter PhysicsPolarization (waves)Electronic Optical and Magnetic MaterialsDipolechemistryControl and Systems EngineeringChemical physicsMaterials ChemistryCeramics and CompositesOptoelectronicsHigh Energy Physics::ExperimentElectretPhysics::Chemical PhysicsElectrical and Electronic EngineeringLangevin dynamicsbusinessIntegrated Ferroelectrics
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Stochastic dynamics of polymer brushes under shear deformation

1998

The dynamical properties of polymer brushes under shear deformation have been studied by computer simulation. Both the local and the global dynamic properties at various shear rates have been calculated. The distribution of orientational and translational mobilities of the different monomers along the chain have been obtained. It was shown that the local mobility of the brushes changes very slowly with increasing of shear rates up to the largest rates. Increase in grafting density leads to an increasingly step like dependence of the correlation times as a function of shear rate.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMineralogy02 engineering and technologyPolymerMechanics010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciencesElectronic Optical and Magnetic MaterialsCondensed Matter::Soft Condensed MatterSimple shearShear rateStochastic dynamicschemistryShear (geology)Materials ChemistryCeramics and Composites0210 nano-technologyJournal of Non-Crystalline Solids
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Development of core-shell colloids to study self-diffusion in highly concentrated dispersions

2007

To study single particle motion in highly concentrated colloidal dispersions, a host-tracer colloid system was developed, consisting of crosslinked polymer micronetwork spheres placed in a good solvent. The host colloid is made invisible to the experimental probe by matching its refractive index to that of the solvent. For the tracer particles a core-shell structure was chosen to ensure the interaction potential to be identical to that of the host particles. Therefore the shell was made of the same polymer as the host. The core differs in refractive index from the solvent and is therefore visible due to scattered light.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesSelf-diffusionMaterials scienceShell (structure)PolymerCondensed Matter::Soft Condensed MatterCore (optical fiber)ColloidchemistryDynamic light scatteringChemical physicsSPHERESRefractive index
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Electronic structure of polysilanes: influence of substitution and conformation

1993

Abstract The valence effective Hamiltonian (VEH) quantum-chemical approach is used to investigate the electronic properties of polysilane. The valence band structure calculated for this fully saturated polymer is analyzed in terms of orbital contributions and compared to that of the closely related carbon polymer, polyethylene. The effects of alkyl substitution and silicon backbone conformation are studied by elucidating the modifications that these structural changes induce on the electronic valence band structure of all-trans unsubstituted polysilane. The VEH results predict a decrease of the band gap upon alkyl substitution and on going from helical to all-trans conformations.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesValence (chemistry)SiliconBand gapMechanical EngineeringMetals and Alloyschemistry.chemical_elementPolymerElectronic structurePolyethyleneCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundsymbols.namesakeCrystallographychemistryMechanics of MaterialsComputational chemistryMaterials ChemistrysymbolsPolysilaneHamiltonian (quantum mechanics)Synthetic Metals
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