Search results for "Spectroscopy"

showing 10 items of 10293 documents

Melt processing of hexa-peri-hexabenzocoronene on the water surface

2011

A discotic polycyclic aromatic hydrocarbon, hexa-peri-hexabenzocoronene, was oriented by slow cooling from the isotropic phase on a water surface as a film. For melt processing at low temperatures, an HBC derivative with long swallow-tailed alkyl side chains was chosen. The supramolecular organization in the resulting thin layer was investigated by electron microscopy. In high-resolution mode, the structural study showed large domains in which the columnar structures were oriented uniaxially with an edge-on arrangement of the hydrophobic molecules. The length of the stacks exceeded several hundred nanometers without obvious defects. The small-area analysis by TEM allowed the direct visualiz…

chemistry.chemical_classificationDiscotic liquid crystalStacking02 engineering and technologySurfaces and Interfaces010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciencesCrystallographyElectron diffractionchemistryTransmission electron microscopyPhase (matter)ElectrochemistrySide chainGeneral Materials Science0210 nano-technologyColumnar phaseSpectroscopyAlkyl
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Imidazolium functionalized carbon nanotubes for the synthesis of cyclic carbonates: reducing the gap between homogeneous and heterogeneous catalysis

2016

Single walled carbon nanotubes (SWCNTs) were functionalized with imidazolium salts bearing vinyl functionalities. An extremely high loading of active species was achieved through a straightforward one-pot procedure involving self-assembly of the imidazolium moieties followed by radical initiated polymerization of the double bonds. The materials were extensively characterized by transmission electron microscopy, Raman spectroscopy, nitrogen physisorption and combustion chemical analysis. The imidazolium functionalized SWCNTs displayed excellent catalytic activity for the reaction of CO2 and epoxides to produce cyclic carbonates as demonstrated by the excellent turnover numbers (TON). Moreove…

chemistry.chemical_classificationDouble bond010405 organic chemistryInorganic chemistrySettore CHIM/06 - Chimica OrganicaCarbon nanotube010402 general chemistryHeterogeneous catalysis01 natural sciencesCatalysis0104 chemical scienceslaw.inventionCatalysissymbols.namesakechemistryPolymerizationPhysisorptionChemical engineeringlawTransmission electron microscopysymbolsRaman spectroscopyCatalysis Science & Technology
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Experimental and theoretical studies on corals. I. Toward understanding the origin of color in precious red corals from Raman and IR spectroscopies a…

2009

An attempt to explain the origin of the vivid red color in precious pink and red corals was undertaken. Raman and IR spectroscopies were applied to characterize white, pink and red corals. The position of the Raman signal near 1500 cm −1 of some corals and pearls was associated by several authors with the presence of the mixture of all-trans-polyenic pigments, containing 6 – 16 conjugated C C bonds or β-carotenoids. This hypothesis was examined theoretically by performing extensive B3LYP-DFT calculations of vibrational spectra of the model polyenic compounds. The B3LYP/6-311++G ∗∗ predicted positions of the dominating Raman mode depend on the number of C Cu nits (Cn parameter) and can be ac…

chemistry.chemical_classificationDouble bondChemistryCoralAnalytical chemistryConjugated systemRed Colorsymbols.namesakePigmentvisual_artsymbolsvisual_art.visual_art_mediumGeneral Materials ScienceRaman spectroscopySpectroscopyVibrational spectraJournal of Raman Spectroscopy
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Bonding in the heavy analogue of hydrogen cyanide: the curious case of bridged HPSi.

2010

The bonding of firstand second-row elements differ dramatically. The simplest unsaturated silicon hydrides Si2H2 and Si2H4 exhibit quite unusual geometries [1] compared to the analogous hydrocarbon molecules. For example, the most stable form of Si2H2 is nonplanar with C2v symmetry and two bridging H atoms, in sharp contrast to linear acetylene, HC! CH. Phosphorus and nitrogen share many of the same bonding characteristics, but P prefers single over multiple bonds. For these reasons, it may be difficult to predict the most stable isomeric arrangement, even for a small molecule with a single Por Si atom and especially when it contains both. Silicon–phosphorus bonds are important in materials…

chemistry.chemical_classificationDouble bondChemistryHydrogen bondGeneral ChemistryPhotochemistryCatalysisBond lengthCrystallographyChemical bondAb initio quantum chemistry methodsMoleculeSingle bondRotational spectroscopyAngewandte Chemie (International ed. in English)
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Structure and properties of N-methyl-N-(4-pyridyl)-nitramine and 1,4-dihydro-1-methyl-4-nitriminopyridine

2002

Abstract The molecular structure and spectral properties of N -methyl- N -(4-pyridyl)-nitramine ( 1 ) and 1,4-dihydro-1-methyl-4-nitriminopyridine ( 3 ) were investigated by the X-ray diffraction, FTIR, nuclear magnetic resonance (NMR) methods and DFT theoretical calculations. N -methyl- N -(4-pyridyl)-nitramine ( 1 ) crystallises in the orthorhombic Pbca space group. It is composed of two planar fragments; nitramino (N 2 O 2 ) group and the pirydyl ring. These two groups are twisted at about 70° with respect to each other, along the Ar–N bond. On the contrary, in compound 3 , they are coplanar to each other. Twist of the nitramino group in 1 with respect to the pirydyl ring leads to a sign…

chemistry.chemical_classificationDouble bondChemistryStereochemistryNMR spectraOrganic ChemistryCarbon-13 NMRRing (chemistry)DFT calculationsAnalytical ChemistryInorganic ChemistryBond lengthNMR spectra databaseCrystallographychemistry.chemical_compoundFTIR spectraPyridineMoleculeOrthorhombic crystal systemX-ray structureN-Nitro compoundsSpectroscopyJournal of Molecular Structure
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Interaction Mechanisms between guaiacols and lignin: the conjugated double bond makes the difference.

2011

Lignin is considered to be responsible for a selective sorption of phenolic compounds on wood. In order to investigate the mechanisms involved, two similar guaiacol compounds--only differing by the nature of the para side chain--were adsorbed on oak wood extracted lignin. Vapor sorption-desorption isotherms indicated that about 3.5 wt % of 4-vinylguaiacol is adsorbed near saturation whereas it is only 0.8% for 4-ethylguaiacol. For both compounds, the isotherms displayed a hysteresis though significantly greater for 4-vinylguaiacol. Analyses of the hydroxyl stretching region of FTIR spectra of the lignin/4-ethylguaiacol and lignin/4-vinylguaiacol complexes indicated that physisorption via hy…

chemistry.chemical_classificationDouble bondHydrogen bondChemistrytechnology industry and agriculturemacromolecular substancesSurfaces and InterfacesConjugated systemCondensed Matter Physicscomplex mixturesNMR spectra databasechemistry.chemical_compoundPhysisorptionDesorptionElectrochemistryLigninOrganic chemistryGeneral Materials ScienceGuaiacolSpectroscopyLangmuir : the ACS journal of surfaces and colloids
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Organometallic ABC-triblock copolymers

1998

The interaction of Fe and Pd complexes with double bonds of the polybutadiene (PB) block in polystyrene-polybutadiene-poly(methyl methacrylate) block copolymers has been studied. The incorporation of Fe(CO)3 fragments into the PB bloc was found to result in an increase in its rigidity. The presence of iron or palladium complexes in the PB block affects strongly the morphology of the triblock copolymers.

chemistry.chemical_classificationDouble bondInfrared spectroscopychemistry.chemical_elementGeneral Chemistrychemistry.chemical_compoundDifferential scanning calorimetryPolybutadienechemistryTransmission electron microscopyPolymer chemistryCopolymerMethyl methacrylatePalladiumRussian Chemical Bulletin
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General and Theoretical Aspects of the Metal Enolates

2010

1 General Aspects 2 Structure of the Metal Enolates 3 Spectroscopy of the Metal Enolates 4 Reactivity of the Metal Enolates 5 Acknowledgments Keywords: general and theoretical aspects of metal enolates; metal enolate structure; calcium and magnesium enolates; spectroscopy of metal enolates - NMR spectroscopy; UV spectroscopy; enolate, applied to anionic structure with two carbon atoms bound through double bond; IR spectroscopy; generalized gradient approximation (GGA-DFT) for adsorption modes of acetone

chemistry.chemical_classificationDouble bondMagnesiumInorganic chemistryInfrared spectroscopychemistry.chemical_elementNuclear magnetic resonance spectroscopyMetalUltraviolet visible spectroscopychemistryvisual_artvisual_art.visual_art_mediumPhysical chemistryReactivity (chemistry)Spectroscopy
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ChemInform Abstract: General and Theoretical Aspects of the Metal Enolates

2010

1 General Aspects 2 Structure of the Metal Enolates 3 Spectroscopy of the Metal Enolates 4 Reactivity of the Metal Enolates 5 Acknowledgments Keywords: general and theoretical aspects of metal enolates; metal enolate structure; calcium and magnesium enolates; spectroscopy of metal enolates - NMR spectroscopy; UV spectroscopy; enolate, applied to anionic structure with two carbon atoms bound through double bond; IR spectroscopy; generalized gradient approximation (GGA-DFT) for adsorption modes of acetone

chemistry.chemical_classificationDouble bondMagnesiumchemistry.chemical_elementInfrared spectroscopyGeneral MedicineNuclear magnetic resonance spectroscopyMetalUltraviolet visible spectroscopychemistryvisual_artvisual_art.visual_art_mediumPhysical chemistryReactivity (chemistry)SpectroscopyChemInform
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The abundance of Au, Pt, Pd, and the mode of heavy metal fixation in highly polluted sediments from the Rhine River near Mainz, West Germany

1984

The Au, Pt and Pd contents of the sediments of Ginsheimer‐Altrhine River, a channel of the Rhine river which drains one of the most industrialized regions of western Europe, have been determined by flameless atomic absorption spectrophotometry. The abundances of these noble metals range from 96–460 ppb Au; 734 ppb‐31 ppm Pt and 32 ppb‐4 ppm Pd. The extremely high concentrations, particulary those of Pt and Pd, are attributed to their use in industry and are due to the formation and concentration of metal‐organic complexes, mainly at the interface between an extremely reducing and an oxidizing aquatic environment. Differential thermal analyses of the polluted sediments in comparison to the p…

chemistry.chemical_classificationEcologyGeography Planning and DevelopmentSedimentchemistry.chemical_elementengineering.materialPollutionSoil contaminationlaw.inventionMetalchemistrylawvisual_artEnvironmental chemistryOxidizing agentvisual_art.visual_art_mediumengineeringHumic acidNoble metalComputers in Earth SciencesAtomic absorption spectroscopyPlatinumWaste Management and DisposalInternational Journal of Environmental Studies
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