Search results for "Spectroscopy"

showing 10 items of 10293 documents

Photodissociation of Formyl Fluoride in Rare Gas Matrixes

2006

Photodissociation of formyl fluoride (HCOF) is studied in Ar, Kr, and Xe matrixes at 248 and 193 nm excitation by following spectral changes in the infrared absorption spectra. In all matrixes, the main photodissociation products are CO/HF species, including CO-HF and OC-HF complexes and thermally unstable CO/HF species (a distorted CO/HF complex or a reaction intermediate), which indicate negligible cage exit of atoms produced via the C-F and C-H bond cleavage channels. However, the observation of traces of H, F, CO, CO(2), F(2)CO, FCO, and HRg(2)(+) (Rg = Kr or Xe) in Kr and Xe matrixes would imply some importance of other reaction channels too. The analysis of the decay curves of the pre…

chemistry.chemical_compoundChemistryPhotodissociationInfrared spectroscopyReaction intermediatePhysical and Theoretical ChemistryPhotochemistryBond cleavageDissociation (chemistry)ExcitationSpectral lineFormyl fluorideThe Journal of Physical Chemistry A
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Antimykotische wirkstoffe. XXI. Aliphatisch und alicyclisch substituierte chlor-diallylamino-1l,3,5-triazine

1988

Aus der nucleophilen Substitution eines Chloratoms in 2,4-Dichlor-6-(diallylamino)-1,3,5-triazin (1) durch Amine (2a-g) gehen die Alkylamino- und Cycloalkylamino-chlor-(diallylamino)-1,3,5-triazine (3a-g) hervor. Von den zur Untermauerung des Strukturtyps 3 herangezogenen spektroskopischen Daten sind besonders charakteristisch die durch das 1,3,5-Triazinringsystem hervorgerufene IR-Bande bei 800 cm−1, die den Allylgruppen zuzuordnenden vier 1H-NMR-Signale zwischen 4,1–6,1 ppm und das beim massenspektroskopischen Abbau auftretende Rumpfkation m/e 158. Auffallend ausgepragt sind in Verbindungsklasse 3 antimykotische, trichomonazide und herbizide Wirksamkeit. By nucleophilic substitution of on…

chemistry.chemical_compoundChemistryStereochemistryOrganic ChemistryChlorine atomNucleophilic substitutionAmine gas treatingStructure typeCyclohexylamineNuclear magnetic resonance spectroscopyRing (chemistry)Journal of Heterocyclic Chemistry
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Synthesis and Conformational Analysis of Saturated3,1,2-Benzoxazaphosphinine 2-Oxides

2005

N-Unsubstituted, N-methyl and N-benzyl cis- and trans-2(hydroxymethyl)cyclohexylamines were subjected to ring closure with phenylphosphonic dichloride, phenyl dichlorophosphate and bis(2-chloroethyl)phosphoramidic dichloride in order to synthesize P-epimeric diastereomers of the corresponding unsubsituted and N-substituted 2-phenyl-, 2phenoxy- and 2-[bis(2-chloroethyl)amino]octahydro-2H3,1,2-benzoxazaphosphinine 2-oxides. The stereochemistry and conformations of the prepared compounds were analyzed mainly by variable-temperature 1 H, 13 C and 31 P NMR spectroscopy. Geometry optimizations were performed for some trans-fused molecules by utilizing the B3LYP DFT method and a locally dense basi…

chemistry.chemical_compoundChemistryStereochemistryOrganic ChemistryDiastereomerMoleculeCyclohexylaminesHydroxymethylNuclear magnetic resonance spectroscopyPhysical and Theoretical ChemistryRing (chemistry)Phenyl dichlorophosphateBasis setEuropean Journal of Organic Chemistry
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Ultrafast energy transfer in dansylated POPAM–eosin complexes

2006

Abstract Excitation energy transfer (EET) in dendritic host–guest complexes has been studied. Three generations G2, G3 and G4 of dansyl substituted poly(propyleneamine) dendrimers (POPAM) were complexed with a fluorescent dye eosin in chloroform solution. Arrival of excitation from dansyls to eosin was monitored by femtosecond transient absorption spectroscopy. EET rates from the dansyls to eosin(s) are characterised by two time constants 1 ps and 6 ps independent of dendrimer generation. Relaxation processes in eosin were clearly faster when complexed with dendrimer than in solution. As several eosins are bound to G3 and G4 dendrimers, besides host–guest interaction, also eosin–eosin inter…

chemistry.chemical_compoundChloroformchemistryEosinDendrimerRelaxation (NMR)FemtosecondUltrafast laser spectroscopyGeneral Physics and AstronomyPhysical and Theoretical ChemistrySpectroscopyPhotochemistryFluorescenceChemical Physics Letters
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Determination of fluoride in rocks, soils, and fluoride-bearing minerals by separation using direct distillation in sulfuric acid medium and spectrop…

1989

Abstract An analytical method for fluoride determination in geological samples is proposed. It is based on a previous fluoride separation by distillation with a Teflon reactor. The variables that influence distillation quantitation (temperature, time, and acid concentration) are optimized. The influence of some species on fluoride recovery during distillation are studied, and conditions to avoid this influence are suggested. Fluoride determination is carried out by means of a spectrophotometric method [La(III)-F−-Alizarin complexone system] (N. T. Crosby, A. L. Dennis, and J. G. Stevens, Analyst (London), 1968, 93, 643–652). The method is applied to the analysis of soils, rocks, and fluorid…

chemistry.chemical_compoundChromatographyAcid concentrationChemistrylawSoil waterSulfuric acidDistillationFluorideSpectroscopyAnalytical Chemistrylaw.inventionMicrochemical Journal
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FIA-Fluorimetric assembly for the determination of noradrenaline hydrochloride by a solid-phase reactor with immobilized hexacyanoferrate(III)

1997

An FIA assembly provided with immobilized hexacyanoferrate(III) is proposed for the fluorimetric determination of noradrenaline hydrochloride. The oxidative reagent is immobilized by means of a strong anion-exchange resin. The FIA manifold is very simple and the calibration graph is linear over the range 0.5–75mgl−1 noradrenaline hydrochloride with an r.s.d of 0.88% (17 replicates) and a sample throughput of 84h−1. Foreign compounds such as NaCl, sucrose, lactose and sodium sulfate caused no significant errors. The procedure is applied to the determination of noradrenaline in a medicinal formulation.

chemistry.chemical_compoundChromatographychemistryHydrochlorideCalibration curveReagentSodium sulfateFluorescence spectrometryQuantitative analysis (chemistry)Dosage formFluorescence spectroscopyAnalytical ChemistryMikrochimica Acta
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Synthesis and characterization of a new Organic – Inorganic sulfate (C5H6N2O)2[Co(H2O)6]3(SO4)4.2H2O

2014

crystals of a new hybrid compound, (C 5 H 6 N 2 O) 2 [Co(H 2 O) 6 ] 3 (SO 4 ) 4 .2H 2 O, were synthesized in aqueous solution and characterized. This compound crystallizes in the triclinic system with the space group P-1, the unit cell :a=6.632(3) A, b=11.769(5) A, c=14.210(6) A, α=67.86(4)°, β=81.32(4)°, γ=85.18(4)° and V=1015.14(8) A 3 . Its crystal structure can be described as a packing of alternated inorganic and organic layers. The different components are connected by a three-dimensional network of O-H…O and N-H…O hydrogen bonds.

chemistry.chemical_compoundCrystallographyAqueous solutionChemistryHydrogen bondBand gapStereochemistryOrganic inorganicInfrared spectroscopyCrystal structureTriclinic crystal systemSulfateJOURNAL OF ADVANCES IN CHEMISTRY
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A macrocyclic diurea derived from diphenylether

2010

Abstract A new 16-membered cyclic diurea was synthesized and tested as potential receptor for fluoride. 1 H and 19 F NMR spectroscopy revealed an unexpected deprotonation of both urea groups after initial 1:1 binding. A single crystal X-ray structure shows bifurcated hydrogen bonds to two DMSO molecules.

chemistry.chemical_compoundCrystallographyDeprotonationchemistryHydrogen bondOrganic ChemistryDrug DiscoveryUreaMoleculeNuclear magnetic resonance spectroscopyBiochemistrySingle crystalFluorideTetrahedron Letters
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Synthesis of a quenchable high-pressure form of magnetite (h-Fe3O4) with composition Fe1(Fe2+0.75Mg0.26)Fe2(Fe3+0.70Cr0.15Al0.11Si0.04)2O4

2014

We report the synthesis of h-magnetite, ideally h-Fe 3 O 4 with considerable amounts of substitutional cations (Cr, Mg, Al, Si) and quenchable to ambient conditions. Two types of experiments were performed at 18 GPa and 1800 °C in a multi-anvil press. In one, we used an oxide mixture with a majoritic stoichiometry Mg 1.8 Fe 1.2 (Al 1.4 Cr 0.2 Si 0.2 Mg 0.2 )Si 3 O 12 , with Si and Mg in excess as starting material (MA-367, MA-380). In the second type of experiment (MA-376), we started from an oxide mixture on the composition of the Fe-oxide phase obtained in MA-367. The Fe-oxide phases of both experiments were investigated by electron microprobe and transmission electron microscopy includin…

chemistry.chemical_compoundCrystallographyGeophysicsElectron diffractionGeochemistry and PetrologyChemistryElectron energy loss spectroscopyFormula unitPhase (matter)OxideElectron microprobeWadsleyiteStishoviteAmerican Mineralogist
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Spin-Transition in [Fe(II)(2,6-Bis-(Benzimidazol-2′-yl)pyridine)2] (CIO4)2: Hysteresis Effect Dependent on the Matrix

1999

Abstract Far-Infrared spectroscopical investigation of the spin-crossover in [Fe(II)(2,6-bis-(benzimidazol-2′-yl)-pyridine)2] (CIO4)2 exhibits a hysteresis in both CsI and polyethylene matrices within temperature cycles between 100K and 520K. The hysteresis broadening is dependent on the matrix and bigger in CsI. This can be explained due to polarity and hydrogen bonding. Two low spin vibrations, LS1 at 437 cm−1 and LS2 at 424cm−1, are observed. On heating from 100K to 520K: during LS1 decreases, the LS2 raises temporarily, until both LS1 and LS2 disappear; for the HS only one raising species was observed. This gives raise to assume two different sub-lattices.

chemistry.chemical_compoundCrystallographyHysteresisNuclear magnetic resonanceSpin statesChemistryHydrogen bondSpin crossoverPyridineSpin transitionInfrared spectroscopyCondensed Matter PhysicsSpin (physics)Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals
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