Search results for "Raman"

showing 10 items of 1328 documents

Raman and theoretical study of the solvent effects on the sizable intramolecular charge transfer in the push-pull 5-(dimethylamino)-5'-nitro-2,2'-bit…

2006

In this paper, we analyze the degree of intramolecular charge transfer in a push-pull π-conjugated system, 5-(dimethylamino)-5'-nitro-2,2'-bithiophene, from changes in frequencies and relative intensities of its strongestRaman scatterings in a bunch of solvents with different polarities. Density functional theory (DFT) was used as a support of the experimental study. Solvent effects on the molecular and electronic structures and on the vibrational properties were estimated by performing B3LYP/6-31G** calculations within the framework of the polarized continuum model (PCM) developed by Tomasi. Calculations reveal that the molecule is highly polarized in the ground state and behaves as a very…

ChemistryPhotochemistryMolecular physicsSolventsymbols.namesakeIntramolecular forcesymbolsMoleculeDensity functional theoryPhysics::Chemical PhysicsPhysical and Theoretical ChemistrySolvent effectsRaman spectroscopyGround stateRaman scatteringThe journal of physical chemistry. A
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Raman spectroscopy and crystal-field split rotational states of photoproducts CO and H2 after dissociation of formaldehyde in solid argon.

2012

Raman signal is monitored after 248 nm photodissociation of formaldehyde in solid Ar at temperatures of 9-30 K. Rotational transitions J = 2 ← 0 for para-H(2) fragments and J = 3 ← 1 for ortho-H(2) are observed as sharp peaks at 347.2 cm(-1) and 578.3 cm(-1), respectively, which both are accompanied by a broader shoulder band that shows a split structure. The rovibrational spectrum of CO fragments has transitions at 2136.5 cm(-1), 2138.3 cm(-1), 2139.9 cm(-1), and 2149 cm(-1). To explain the observations, we performed adiabatic rotational potential calculations to simulate the Raman spectrum. The simulations indicate that the splitting of rotational transitions is a site effect, where H(2) …

ChemistryPhotodissociationGeneral Physics and AstronomyRotational–vibrational spectroscopyDissociation (chemistry)symbols.namesakeExcited statesymbolsMoleculeRotational spectroscopyPhysical and Theoretical ChemistryAtomic physicsTriplet stateRaman spectroscopyta116The Journal of chemical physics
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Gold catalysts supported on CeO2 and CeO2–Al2O3 for NO reduction by CO

2006

Abstract The reduction of NO x by CO was studied over gold catalyst supported on ceria and ceria–alumina. The mixed supports with different CeO 2 /Al 2 O 3 ratios were prepared by co-precipitation. The catalysts were characterized by means of XRD, TPR, XPS and Raman spectroscopy. The addition of alumina led to a slight enlargement of the gold particles, while the ceria particle size was decreased. Deeper oxygen vacancies formation in the presence of alumina was detected by TPR, XPS and Raman spectroscopy, compared to the pure ceria support. The samples exhibited a high and stable activity and 100% selectivity towards N 2 was reached at 200 °C.

ChemistryProcess Chemistry and TechnologyCatalyst supportInorganic chemistryHeterogeneous catalysisCatalysisCatalysischemistry.chemical_compoundsymbols.namesakeX-ray photoelectron spectroscopyTransition metalAluminium oxidesymbolsParticle sizeRaman spectroscopyGeneral Environmental ScienceApplied Catalysis B: Environmental
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Effect of Ti(IV) loading on CO oxidation activity of gold on TiO2 doped amorphous silica

2006

Abstract Amorphous SiO 2 , doped with various amount of TiO 2 , was used as support for gold nanoparticles. Gold was deposited through the controlled sol formation technique. The effect of the TiO 2 loading on the structural and surface properties was investigated by transmission electron microscopy, X-ray diffraction, Raman and X-ray photoelectron spectroscopy. The catalytic behavior was tested in the oxidation of CO. A significant enhancement in the activity was observed for the gold supported on mixed oxide with low TiO 2 loading. On the basis of characterization data, the positive effect is assigned to the electronic modification of the Ti(IV) of the newly formed Ti O Si bonds.

ChemistryProcess Chemistry and TechnologyInorganic chemistrytechnology industry and agricultureNanoparticleCatalysisAmorphous solidsymbols.namesakeTransition metalX-ray photoelectron spectroscopyTransmission electron microscopyColloidal goldsymbolsMixed oxideRaman spectroscopyApplied Catalysis A: General
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Structural characterisation of silica supported CoMo catalysts by UV Raman spectroscopy, XPS and X-ray diffraction techniques

2002

The structure of Co-Mo catalysts supported on commercial silica, doped with various amounts of sodium ions, was investigated by means of X-ray diffraction (XRD), UV-Raman spectroscopy and X-ray photoelectron spectroscopy (XPS). Two series of samples were considered. One series was prepared by classic incipient wet impregnation (WI) and the other series by co-impregnation in the presence of nitrilotriacetic acid (NTA). The effect of sodium on the catalyst structure depended on the preparation procedure: in the case of the WI catalysts, sodium promoted the transformation of the polymolybdate species into monomolybdate Na2MoO4; in the case of the NTA prepared samples, sodium induced transforma…

ChemistryProcess Chemistry and TechnologySodiumInorganic chemistrychemistry.chemical_elementCatalysisCatalysissymbols.namesakechemistry.chemical_compoundX-ray photoelectron spectroscopyTransition metalX-ray crystallographysymbolsThiopheneSpectroscopyRaman spectroscopyApplied Catalysis A: General
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Structural and spectroscopic study of the Br2...3-Br-pyridine complex by DFT calculations.

2007

Abstract The structure and the Raman vibrational spectrum of the complex Br 2 ⋯3-Br-pyridine are determined by DFT calculations using different parametrizations. The calculations are performed taking into account the effects of the dichloromethane as solvent by the CPCM method. A value of 39 kJ mol −1 for the formation enthalpy and of 1 kJ mol −1 for the formation free energy at room temperature in presence of the solvent is found. The predicted Raman spectrum is compared with the experimental one and the essential features of the spectrum are well reproduced by the B3LYP parametrization. The intensity changes of the bands when going from the free moieties to the complex are also generally …

ChemistryPyridinesEntropyEnthalpyMolecular ConformationVibrational spectrumBromineSpectrum Analysis RamanAtomic and Molecular Physics and OpticsAnalytical ChemistrySolventchemistry.chemical_compoundsymbols.namesakeModels ChemicalComputational chemistryPyridinesymbolsPhysical chemistrySolvent effectsRaman spectroscopyInstrumentationParametrizationSpectroscopyDichloromethaneSpectrochimica acta. Part A, Molecular and biomolecular spectroscopy
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High-resolution photoacoustic Raman spectroscopy of gases

1992

A high-resolution photoacoustic Raman spectroscopy experiment is described. The resolution achieved by using two single-mode pulsed lasers is about 0.0054 cm −1 (full width at half maximum intensity). The experiment was tested first on the v 1 /2v 2 bands of CO 2 and gave an increase of at least about one order of magnitude in the signal-to-noise ratio with respect to stimulated Raman spectroscopy at low pressure (ca. 10 Torr ≃ 1.3 kPa). The sensitivity is also demonstrated by the study of the weak hot band v 1 +v 2 −v 2 of CO 2 . In both cases, the experimental line shape is well reproduced by taking into account Doppler and collisional effects. A comparison with CARS spectra was also made

ChemistryResolution (electron density)Analytical chemistryLaserHot bandSpectral linelaw.inventionsymbols.namesakeFull width at half maximumlawsymbolsGeneral Materials ScienceRaman spectroscopySpectroscopyDoppler effectSpectroscopyJournal of Raman Spectroscopy
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State-to-state vibrational and rotational energy transfer in CO2 gas from time-resolved raman-infrared double resonance experiments

1998

A time-resolved Raman–infrared double resonance technique was used to study collisional relaxation rates of vibrational and rotational energy levels in CO2 gas at 295 K. A pulsed Raman excitation populated a selected rovibrational initial state. Measurements of the rates of transfer from the pumped initial state into specific final states were carried out using time-resolved laser absorption spectroscopy. First, the transfer rates were determined for the five lower vibrational energy levels. In particular, it was confirmed that the rate of transfer between the two Fermi levels (1000) and (0200) is very small [(5.3±0.2)×104 Torr-1 s-1]. The rotational structure inside the (0200) vibrational …

ChemistryRotational transitionRotational temperatureRotational–vibrational spectroscopyKinetic energyRotational energysymbols.namesakesymbolsVibrational energy relaxationGeneral Materials ScienceRotational spectroscopyAtomic physicsRaman spectroscopySpectroscopyJournal of Raman Spectroscopy
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MOCVD growth of CdTe on glass: analysis of in situ post-growth annealing

2004

Abstract In this paper, we analyse the growth by MOCVD of CdTe on glass substrates using in situ post-growth annealing. First, in order to perform a systematic study, polycrystalline layers of CdTe were deposited by MOCVD on glass substrates. The structure and morphology of the layers was investigated as a function of different growth parameters, temperature, VI/II precursor molar ratio and substrate position on the susceptor. An activation energy of Ek=20.7 kcal/mol was obtained from the experimental data. In order to better understand the process and the effects of different growth parameters, a numerical model that simulated the gas flow in the reactor, was developed. Secondly we analyse…

ChemistryScanning electron microscopeSubstrate (electronics)Activation energyCondensed Matter PhysicsCadmium telluride photovoltaicsAnnealing (glass)Inorganic ChemistryCrystallographysymbols.namesakeChemical engineeringMaterials ChemistrysymbolsCrystalliteMetalorganic vapour phase epitaxyRaman spectroscopyJournal of Crystal Growth
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Synthesis, Crystal Structure, and Properties of Multicomponent Bis(ethylenedithio)tetrathiafulvalene Charge-Transfer Salts of the [Mo3S7Br6]2- Cluster

2005

A new family of bis(ethylenedithio)tetrathiafulvalene (ET) radical salts has been prepared in the presence of a triangular molybdenum sulfide cluster of formula [Mo 3 S 7 Br 6 ] 2 - , which contains highly electrophilic axialsulfur atoms. A systematic change in the experimental conditions yields five different salts, namely (ETA)2(ET B )[Mo 3 S 7 Br 6 ] 2 . CH 2 Br 2 (1), (ETA)(ET B )Mo 3 S 7 Br 6 ].1.1CH 2 Br 2 (2), (ETA)(ETB)(ET C ){[Mo 3 S 7 Br 6 ]Br}.0.5C 2 H 4 Cl 2 (3), (ET)((n-Bu 4 )N)-[Mo 3 S 7 Br 6 ] (4), and (ET)(Ph4P)[Mo 3 S 7 Br 6 ].0.5CH 3 CN (5), where the ET subscript denotes crystallographically independent molecules. The five compounds have been structurally characterized, a…

ChemistryStereochemistryCrystal structureTriclinic crystal systemSpectral lineInorganic ChemistryCrystallographysymbols.namesakechemistry.chemical_compoundElectrophilesymbolsMoleculePhysical and Theoretical ChemistryRaman spectroscopyStoichiometryTetrathiafulvaleneInorganic Chemistry
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