Search results for "Spectroscopy"

showing 10 items of 10293 documents

Absorption spectrum of the f(A1g) ← X(Eg), a(F2g) electronic transition of OsF6

1997

Abstract The absorption spectrum of the visible band of OsF 6 has been recorded using a commercial spectrophotometer. The first vibronic assignments for this band have been realized using the analogy with the d ← X transition of IrF 6 . Some vibronic parameter values are derived.

chemistry.chemical_compoundAbsorption spectroscopyChemistryVisible bandVibronic spectroscopyAtomic physicsOsmium hexafluorideInstrumentationSpectroscopyAtomic and Molecular Physics and OpticsMolecular electronic transitionAnalytical ChemistrySpectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy
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Erweiterte Konjugation in unsymmetrischen Stilbenylsquarainen

1998

Extended Conjugation in Stilbenylsquaraines Unsymmetrical 1-aryl-3-stilbenylsquaraines 2a–e and 1,3-bis(stilbenyl)squaraines 3a–c were prepared by CC coupling reactions of the corresponding substituted arenes with derivatives of squaric acid (Schemes 2 and 3). Dialkylamino and alkoxy groups enhance the solubility of these dyes and enlarge the intramolecular charge transfer of these donor–acceptor–donor systems. The extended conjugation of the stilbene units – in comparison with arene building blocks – leads to significant bathochromic shifts in the Vis/NIR absorption spectra.

chemistry.chemical_compoundAbsorption spectroscopychemistryIntramolecular forceBathochromic shiftAlkoxy groupSquaric acidSolubilityPhotochemistryMedicinal chemistryCoupling reactionJournal f�r Praktische Chemie/Chemiker-Zeitung
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Polycondensed nitrogen heterocycles. Part19. Pyrrolo[1,2-f]phenanthridines by pschorr-type cyclization brought about by hypophosphorous acid

1986

Pyrrolo[1,2-f]phenanthridines were prepared in good yields by the diazotization in acetic acid of the amines la,b and subsequent treatment with hypophosphorous acid. The necessity for hypophosphorous acid in the reaction was demonstrated.

chemistry.chemical_compoundAcetic acidHypophosphorous acidchemistryOrganic ChemistryOrganic chemistrychemistry.chemical_elementNuclear magnetic resonance spectroscopyNitrogenJournal of Heterocyclic Chemistry
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Rotational State Change of Acetonitrile Vapor on MCM-41 upon Capillary Condensation with the aid of Time-Correlation Function Analysis of IR Spectros…

2000

The infrared spectra of adsorbed acetonitrile on MCM-41 (porewidth = 3.2 nm) were measured at 303 K. In the CN stretching ν2 region, two bands were observed at 2265 cm− 1 and 2254 cm− 1, assigned to hydrogen-bonded molecules on surface hydroxyls of MCM-41, and physisorbed molecules in mesopores, respectively. We designate here the 2265 cm− 1 band as the ν2α band and the 2254 cm− 1 band as the ν2β band. The bandwidth of the fundamental transition ν2fβ, was obtained by removing the overlap with hot band transitions of the same mode, ν2α band, and other modes by least-squares fitting. Before capillary condensation, the relaxation time τ obtained from the bandwidth of the ν2fβ band was smaller …

chemistry.chemical_compoundAdsorptionCapillary condensationMCM-41chemistryAnalytical chemistryInfrared spectroscopyMoleculeMesoporous materialAcetonitrileHot band
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Trichomonazide Wirkstoffe, 5. Mitt. (Dichloranilino)ethentricarbonitrile

1986

chemistry.chemical_compoundAntiprotozoal AgentNitrileChemistryDrug DiscoveryPharmaceutical ScienceNuclear magnetic resonance spectroscopyCombinatorial chemistryArchiv der Pharmazie
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Fluorescence Probe and Scanning Force Microscopic Studies of Water Soluble Comb-Shaped Copolymers Consisting of a Hydrophobic Poly(p-alkylstyrene) Ma…

2002

Fluorescence Probe and Scanning Force Microscopic Studies of Water Soluble Comb-Shaped Copolymers Consisting of a Hydrophobic Poly( p -alkylstyrene) Main Chainand Hydrophilic Poly(ethylene oxide) Grafted Chains

chemistry.chemical_compoundAqueous solutionWater solublePolymers and PlasticsEthylene oxideChemistryPolymer chemistryMaterials ChemistryOxideCopolymerPyreneFluorescenceFluorescence spectroscopyPolymer Journal
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A Mössbauer study of the crystalline structure of the passive film formed on iron in aqueous sulfate solution containing sulfite in low concentration

1993

Electrochemically induced passivation of evaporated, enriched 57Fe in 0.5 mol dm−3 Na2SO4 + 0.001 mol dm−3 NaHSO3 aqueous solution (pH 6.5) was followed by conversion electron Mossbauer spectroscopy. The transformation of amorphous iron oxide or hydroxide into crystalline γ-FeOOH could be observed with the increase of the polarization time. The comparison of the original quantity of evaporated, enriched 57Fe layer on the surface of the samples with the dissolved iron, measured in the solutions after the polarization, proved the existence of pitting corrosion at this pH.

chemistry.chemical_compoundAqueous solutionchemistryPassivationConversion electron mössbauer spectroscopyGeneral Chemical EngineeringInorganic chemistrySodium sulfateElectrochemistryIron oxidePitting corrosionHydroxideSodium sulfiteElectrochimica Acta
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Trace element determination in sediments: a comparative study between neutron activation analysis (NAA) and inductively coupled plasma-mass spectrome…

2000

An inductively coupled plasma-mass spectrometry (ICP-MS) method has been employed for trace element determination in five real sediment samples and a standard reference material. These samples were mineralized by dry ashing at 550°C and fused at 1100°C for 30 min with lithium metaborate. Dissolved samples were measured by a semiquantitative methodology with external calibration and with Rh as an internal standard. More than 50 elements have been measured. As a reference technique, a direct analysis of the solid samples was carried out by neutron activation analysis. Results obtained by ICP-MS have been compared with those obtained by neutron activation analysis (NAA) by applying the paired …

chemistry.chemical_compoundAshingChemistryAnalytical chemistryTrace elementSample preparationNeutron activation analysisMass spectrometryInductively coupled plasma mass spectrometrySpectroscopyAnalytical ChemistryNeutron activationLithium metaborateMicrochemical Journal
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Inverse correlated 1H-13C in vivo NMR as a probe to follow the metabolism of unlabeled vanillin by plant cell cultures

1997

Abstract Inverse correlated 2D 1H-13C NMR spectroscopy was used to follow the metabolism of vanillin (1) in vivo by plant cell suspension cultures of Nicotiana plumbaginifolia at the natural abundance of 13C. Under the non-invasive conditions four products could be detected: vanillylalcohol (2), vanillinglucoside (3) and the phenolic and benzylic glucosides of vanillylalcohol (4 and 5).

chemistry.chemical_compoundBiochemistrychemistryIn vivoVanillinOrganic ChemistryDrug DiscoveryMetabolismNuclear magnetic resonance spectroscopyNicotiana plumbaginifoliaPlant cellBiochemistrySuspension cultureTetrahedron
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Characterization of Interaction Between Humic Acids and Buckminsterfullerene Using Flourescene Spectroscopy

2017

The interaction between buckminsterfullerene C60 and humic acids (HA) of different origins was compared using fluorescence spectroscopy as a function of pH, humic acid concentration, ionic strength. Binding constants between fullerene and humic acids were calculated. It can be suggested that the complexation was driven by hydrophobic interactions depending on the properties of the interacting compounds. Hydrophobic interaction model as indicated by linear Stern-Volmer plots and high Kd values is characterizing the interaction between buckminsterfullerene C60 and humic acids The results of this study support the development of an understanding of the fate of nanomaterials in the environment …

chemistry.chemical_compoundBuckminsterfullereneComputational chemistryChemistrySpectroscopycomplex mixturesCharacterization (materials science)Linnaeus Eco-Tech
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