Search results for "Spectroscopy"

showing 10 items of 10293 documents

Densities and viscosities of imidazolium and pyridinium chloroaluminate ionic liquids

2013

Abstract The chloroaluminate ionic liquids are used in various types of reactions. However, due to their particular vulnerability on water, their physical properties have not been previously investigated very extensively. The densities and viscosities of series imidazolium and pyridinium chloroaluminate ionic liquids having alkyl (butyl, hexyl, octyl) or aralkyl (benzyl, ethylphenyl) chain at the cation, various effective molar fraction of AlCl 3 (χ AlCl3  = 0.5, 0.65, 0.7), as well as they mixture and mixture with common organic solvents (hexane, toluene) were measured at the temperature range 293.15–343.15 K (20–70 °C). Densities, and particularly viscosities decrease with the increase of…

chemistry.chemical_classificationdensityInorganic chemistryCondensed Matter PhysicsMole fractionTolueneAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic MaterialsHexaneViscositychemistry.chemical_compoundchemistryIonic liquidviscosityMaterials ChemistrySide chainPyridiniumPhysical and Theoretical ChemistrySpectroscopyAlkylionic liquidJournal of Molecular Liquids
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Deuteron Magnetic Resonance Study of Order and Dynamics in Liquid Crystal Polymers

1984

Abstract Thermotropic nematic polyesters, specifically deuterated at different positions of the polymer chain are studied by multiple pulse dynamic NMR. Analysis of the NMR experiments is achieved, employing a comprehensive model, based on the stochastic Liouville equation. Computer simulations provide the orientational distributions and conformations of the polymer chains and the correlation times of the various motions. In the anisotropic melt the correlation times for chain reorientation and trans-gauche-isomerization are in the range of 0.1–10 ns. Decreasing the temperature of the solid polymer first freezes the intermolecular motions. Thus, below the glass transition only intramolecula…

chemistry.chemical_classificationeducation.field_of_studyChemistryPopulationIntermolecular forceNuclear magnetic resonance spectroscopyPolymerThermotropic crystalCrystallographyLiquid crystalChemical physicsIntramolecular forceeducationGlass transitionMolecular Crystals and Liquid Crystals
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Spin transition in heptanuclear star-shaped iron(III)–antimony(V) NCS- and CN-bridged compounds

2009

Abstract The precursor [FeIII(L)Cl] (LH2 = N,N′-bis(2′-hydroxy-benzyliden)-1,6-diamino-3-azahexane) has been prepared and Mossbauer spectroscopy assigned a high-spin (S = 5/2) state at room temperature. The precursor is combined with the bridging units [SbV(X)6]− (X = CN−, NCS−) to yield star-shaped heptanuclear clusters [(LFeIII–X)6SbV]Cl5. The star-shaped compounds are in general high-spin systems at room temperature. On cooling to 20 K some of the iron(III) centers switch to the low-spin state as indicated by Mossbauer spectroscopy, i.e. multiple electronic transitions. While the cyano-bridged complex performs a multiple spin transition the thiocyanate-compound shows no significant popul…

chemistry.chemical_classificationeducation.field_of_studyCondensed matter physicsPopulationSpin transitionchemistry.chemical_elementInorganic ChemistryCrystallographychemistryAntimonyAtomic electron transitionMössbauer spectroscopyMaterials ChemistryPhysical and Theoretical ChemistryBridged compoundseducationPolyhedron
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Synthesis, molecular structure, spectroscopic properties and stability of (Z)-N-methyl-C-2,4,6-trimethylphenylnitrone.

2015

Abstract New N-methyl-C-2,4,6-trimethylphenylnitrone 1 has been synthesized starting from N-methylhydroxylamine and mesitaldehyde. The product was fully characterized using different spectroscopic techniques; FTIR, NMR, UV–Vis, high resolution mass spectrometry and X-ray diffraction. The relative stability and percent of population of its two possible isomers (E and Z) were calculated using the B3LYP/6-311++G(d,p) method in gas phase and in solution. In agreement with the X-ray results, it was found that Z-isomer is the most stable one in both gas phase and solution. The molecular geometry, vibrational frequencies, gauge-including atomic orbital (GIAO), and chemical shift values were also c…

chemistry.chemical_classificationeducation.field_of_studyspectroscopynitronesPopulationAnalytical chemistryAtomic and Molecular Physics and OpticsAnalytical ChemistryNitroneMolecular geometryAtomic orbitalchemistryPolarizabilityMoleculeHypsochromic shifteducationInstrumentationta116Natural bond orbitalSpectrochimica acta. Part A, Molecular and biomolecular spectroscopy
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Synthesis and thermoresponsive properties of four arm, amphiphilic poly(tert-butyl-glycidylether)-block-polyglycidol stars

2011

Abstract A series of four arm stars with copolymer arms composed of poly(tert-butyl-glycidylether)-b-polyglycidol were prepared using a multi-step process based on anionic ring-opening polymerization. Control of the length of the arms and the number of functional (hydroxyl) reactive groups was achieved by anionic polymerization. Stars with molar masses up to 12200 g/mol were prepared. The amphiphilic character of the star structure was varied using different polyglycidol block lengths. The star structure and molar mass of the obtained stars were characterized by SEC–MALLS and NMR spectroscopy. The temperature behavior of an aqueous solution of the obtained polymers was also investigated. Th…

chemistry.chemical_classificationendocrine systemMaterials scienceMolar massAqueous solutionPolymers and PlasticsOrganic ChemistryNuclear magnetic resonance spectroscopyPolymerAnionic addition polymerizationchemistryPolymerizationAmphiphilePolymer chemistryMaterials ChemistryCopolymerPolymer
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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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H-NMR and FT-IR study of the state of melatonin confined in membrane models: location and interactions of melatonin in water free lecithin and AOT re…

2004

The state of melatonin confined either in dry lecithin or bis(2-ethylhexyl) sulfosuccinate sodium salt (AOT) reversed micelles has been investigated by H-NMR and FT-IR spectroscopies as a function of the melatonin to surfactant molar ratio (R). The analysis of experimental results leads to hypothesize that, independently of R and the surfactant nature and as a consequence of anisotropic melatonin/surfactant interactions, melatonin is totally solubilized in reversed micelles and mainly located by opportune orientation in the nanodomain constituted by the surfactant head groups. The absence of significant spectral changes related to the protons linked to the first carbon atoms of surfactant a…

chemistry.chemical_classificationendocrine systemfood.ingredientOrganic ChemistryPhotochemistryMicelleLecithinlcsh:QD241-441MelatoninfoodMembranelcsh:Organic chemistrychemistryPulmonary surfactantmedicineProton NMRFourier transform infrared spectroscopyhormones hormone substitutes and hormone antagonistsAlkylmedicine.drugArkivoc
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Structure elucidation of new oleanane-type glycosides from three species of Acanthophyllum

2010

From the roots of three species of Acanthophyllum (Caryophyllaceae), two new gypsogenic acid glycosides, 1 and 2, were isolated, 1 from A. sordidum and A. lilacinum, 2 from A. elatius and A. lilacinum, together with three known saponins, glandulosides B and C, and SAPO50. The structures of 1 and 2 were established mainly by 2D NMR techniques as 23-O-β-D-galactopyranosylgypsogenic acid-28-O-β-D-glucopyranosyl-(13)-[β-D-glucopyranosyl-(16)]-β-D-galactopyranoside (1) and gypsogenic acid-28-O-β-D-glucopyranosyl-(13)-[β-D-glucopyranosyl-(16)]-β-D-galactopyranoside (2). The cytotoxicity of several of these saponins was evaluated against two human colon cancer cell lines (HT-29 and HCT 116). Copyr…

chemistry.chemical_classificationfood.ingredientbiologyStereochemistryGlycosideCaryophyllaceaeGeneral Chemistrybiology.organism_classificationAcanthophyllumHuman colon cancerchemistry.chemical_compoundfoodchemistryGeneral Materials ScienceCytotoxicityTwo-dimensional nuclear magnetic resonance spectroscopyOleananeMagnetic Resonance in Chemistry
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Carbon nanostructures incorporated on methacrylate monoliths for separation of small molecules by nano-liquid chromatography

2018

Abstract Carbon nanostructures have been incorporated to polymethacrylate monoliths to develop novel stationary phases with enhanced separation performance in nano-liquid chromatography (nano-LC). Two incorporation approaches of these nanomaterials in monoliths were investigated. Single-walled carbon nanohorns (SWNHs) were first incorporated to the polymerization mixture, followed by UV initiation. The resulting stationary phases with embedded SWNHs led to an increase in the separation performance of analytes compared to the parent monolith. Alternatively, a two-step photo-grafting approach was also adopted to attach the carbon nanoparticles onto the polymer monolith surface. The effect of …

chemistry.chemical_classificationgeographyMaterials sciencegeography.geographical_feature_categoryScanning electron microscope010401 analytical chemistrychemistry.chemical_element02 engineering and technologyCarbon nanotubePolymer021001 nanoscience & nanotechnologyMethacrylate01 natural sciences0104 chemical sciencesAnalytical Chemistrylaw.inventionNanomaterialschemistryChemical engineeringPolymerizationlawMonolith0210 nano-technologyCarbonSpectroscopyMicrochemical Journal
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Selective recognition of aromatic hydrocarbons by endo-functionalized molecular tubes via C/N-H⋅⋅⋅π interactions

2018

Abstract Molecular recognition of aromatic hydrocarbons by four endo -functionalized molecular tubes has been studied by 1 H NMR spectroscopy, computational methods, and single crystal X-ray crystallography. The binding selectivity is rationalized by invoking shape complementarity and dipole alignment. The non-covalent interactions are proved to predominantly be C/N-H⋅⋅⋅ π interactions.

chemistry.chemical_classificationhydrogen bond010405 organic chemistryHydrogen bondStereochemistrySupramolecular chemistryGeneral Chemistry010402 general chemistry01 natural sciencesmolecular dynamics0104 chemical sciencesMolecular recognitionmacrocycleschemistryhydrogenProton NMRhost-guest chemistryaromatic hydrocarbonhydrocarbonsmolecular recognitionAromatic hydrocarbonSpectroscopyHost–guest chemistryta116Binding selectivityChinese Chemical Letters
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