Search results for "Spectroscopy"

showing 10 items of 10293 documents

Up-conversion processes in NaLaF4:Er3+

2009

abstract Structural and spectroscopic investigation of NaLaF 4 :Er 3+ material at different doping concentrations ispresented. X-ray diffraction patterns, up-conversion luminescence spectra and decay curves for 2 H 9/2 ? 4 I 15/2 , 4 S 3/2 ? 4 I 15/2 and 4 F 9/2 ? 4 I 15/2 optical transitions in the material are shown and possibleexcitation routes are discussed. Raman spectrum for the undoped material is presented and the effectivephonon energy of the material is estimated. Based on the obtained results application of rare-earth dopedNaLaF 4 in the field of up-conversion phosphors is evaluated. 2009 Elsevier B.V. All rights reserved. 1. IntroductionFor many years rare-earth (RE) doped materi…

ChemistryOrganic ChemistryDopingAnalytical chemistryNonlinear opticsPhosphorAtomic and Molecular Physics and OpticsPhoton upconversionElectronic Optical and Magnetic MaterialsIonInorganic Chemistrysymbols.namesakesymbolsElectrical and Electronic EngineeringPhysical and Theoretical ChemistryAtomic physicsTime-resolved spectroscopyLuminescenceRaman spectroscopySpectroscopyOptical Materials
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Über gemischte Gruppe 14—Gruppe 14-Bindungen

1991

Abstract p-Tol6PbSn has been synthesized by reaction of p-Tol3PbLi with p-Tol3SnI in THF/ether (1:2) at −78°C. The crystal structures of p-Tol4Pb (I 4 ) and of p-Tol6Sn2, p-Tol6PbSn and p-Tol6Pb2 have been determined. The three dinuclear compounds crystallize not strickly isomorphous. They exhibit the same space group (R 3 and rather similar unit cell dimensions. Yet according to the solvent of crystallization, two types with differing atomic position parameters can be distinguished (“homoeotypism with differences of parameters” in the definition of Laves). In both types, the individual molecules have a chiral C3-symmetric conformation and the non-chiral unit cell encloses both enantiomers.…

ChemistryOrganic ChemistryEtherCrystal structureBiochemistrylaw.inventionInorganic ChemistrySolventchemistry.chemical_compoundCrystallographysymbols.namesakeGroup (periodic table)lawMaterials ChemistrysymbolsMoleculePhysical and Theoretical ChemistryEnantiomerCrystallizationRaman spectroscopyJournal of Organometallic Chemistry
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Electric field induced alignment-orientation conversion in diatomic molecules: analysis and observation for NaK

1999

This article reports the observation of the molecular fluorescence circularity under irradiation with linearly polarised light. This alignment-orientation conversion phenomenon arises as a result of partial transformation from alignment of the ensemble of 1 P state molecular angular momenta into their orientation under the effect of non-linear dc Stark effect. Circularity rate up to 0.12 was observed in D 1 P! X 1 S fluorescence of 23 Na 39 K molecules in agreement with the theoretically predicted value.

ChemistryOrganic ChemistryFluorescenceDiatomic moleculeAnalytical ChemistryInorganic Chemistrysymbols.namesakeStark effectOrientation (geometry)Electric fieldsymbolsMoleculeIrradiationAtomic physicsSpectroscopyNAKJournal of Molecular Structure
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5-Alkenyl-1,2,3-thiadiazole

1986

Es wird die Herstellung der Titelverbindungen 5 durch Bromierung-Dehydrobromierung entsprechender 5-Alkyl-1,2,3-thiadiazole 3, ihre spektroskopische Charakterisierung und ihre Umsetzung mit 4-Phenyl-4H-1,2,4-triazol-3,5-dion (6) zu 7, 8 beschrieben. 5-Alkenyl-1,2,3-thiadiazoles A method of preparation for the title compounds 5, by bromination-dehydrobromination of the corresponding 5-alkyl-1,2,3-thiadiazoles 3, their spectroscopical characterization, and the reaction of 5 with 4-phenyl-4H-1,2,4-triazole-3,5-dione (6) with formation of 7, 8 is described.

ChemistryOrganic ChemistryHalogenationNuclear magnetic resonance spectroscopyPhysical and Theoretical ChemistryMedicinal chemistryCycloadditionLiebigs Annalen der Chemie
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Crystal and molecular structure of anhydrous betaine, (CH3)3NCH2CO2

1999

Abstract 1–Carboxy–N,N,N–trimethylmethanamanium inner salt or anhydrous betaine, (CH3)3NCH2CO2, FW=117.15 gmol −1 , crystallizes in the orthorhombic space group Pnma with a=14.544(2) A , b=6.859(3) A , c=6.131(1) A , V=611.7(3) A 3 , Z=4, D x =1.27 Mgm −3 , λ (MoK α )=0.71073 A , μ =0.091 mm −1 . The structure was resolved by direct methods and refined by least-square calculations to R=0.038 for 531 reflections. Observed changes in bond angles imply that there is a repulsion between nitrogen and oxygen. The melting point (measured at onset) is 570 K. FTIR spectra of anhydrous betaine and monohydrate were recorded. Clear differences were found between the two compounds based on infrared (i.r…

ChemistryOrganic ChemistryInorganic chemistryCrystal structureAnalytical ChemistryInorganic ChemistryCrystalCrystallographychemistry.chemical_compoundMolecular geometryBetaineMelting pointAnhydrousOrthorhombic crystal systemAbsorption (chemistry)SpectroscopyJournal of Molecular Structure
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Crystal structures and thermal behavior of bis[dibenzyldimethylammonium]CuBr4, bis[dibenzyldimethylammonium]CuCl4 and bis[dimethyldi(2-phenylethyl)am…

2006

Abstract Bis[dibenzyldimethylammonium]CuBr4, bis[dibenzyldimethylammonium]CuCl4 and bis[dimethyldi(2-phenylethyl)ammonium]CuBr4 were crystallized from acetonitrile and/or dilute HX solutions. Five different kinds of single crystals were obtained. In the case of bis[dibenzyldimethylammonium]CuX4 (X=Br or Cl), the acetonitrile molecules cocrystallized into the crystal structure when acetonitrile solution was used. As a result, the isomorphic structures of Bis[dibenzyldimethylammonium]CuX4·0.5 CH3CN (X=Br or Cl) in monoclinic space group P21/n were obtained. When a dilute HX solution was used, the bis[dibenzyldimethylammonium]CuX4 (X=Br or Cl) crystallized without solvent molecules. The formed…

ChemistryOrganic ChemistryInorganic chemistryCrystal structureTriclinic crystal systemAnalytical ChemistryInorganic ChemistrySolventchemistry.chemical_compoundCrystallographyMelting pointThermal analysisAcetonitrileSpectroscopyPowder diffractionMonoclinic crystal systemJournal of Molecular Structure
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Properties of new low melting point quaternary ammonium salts with bis(trifluoromethanesulfonyl)imide anion

2010

Eight new monocationic quaternary ammonium (QA) salts with the bis(trifluoromethanesulfonyl)imide (TFSI) anion were prepared by metathesis using our previously reported QA halides as precursors. New salts were characterized both in liquid and solid state using 1 H and 13 C NMR techniques, mass spectroscopy and elemental analysis together with X-ray diffraction and thermoanalytical methods. In addition, residual water content, viscosity and conductivity measurements were made for three of the roomtemperature ionic liquids (RTILs). The crystal structures of three compounds were determined by X-ray single crystal diffraction. Powder diffraction was used to study the crystallinity of the solid …

ChemistryOrganic ChemistryInorganic chemistryHalideCrystal structureAnalytical ChemistryFreezing pointInorganic ChemistryCrystallinitychemistry.chemical_compoundX-ray crystallographyIonic liquidPhysical chemistryThermal analysisSpectroscopyPowder diffractionJournal of Molecular Structure
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Studies in organic mass spectrometry. Part 25. Benzyl ion formation in chemical ionisation (methane or isobutane) of someortho-alkylhetero-substitute…

2000

The behaviour of some ortho-alkylhetero-substituted diphenylcarbinols, including deuterium labelled derivatives, under chemical ionisation (methane or isobutane) conditions has been investigated. It has been determined that ortho-alkylhetero diphenylmethyl cations formed by water elimination from the protonated molecule undergo consecutive rearrangements which afford benzyl (or tropylium) ions previously observed for ortho-substituted diphenylcarbenium ions generated by electron ionisation. This reaction also occurs under low-energy collision conditions. Copyright © 2000 John Wiley & Sons, Ltd.

ChemistryOrganic ChemistryInorganic chemistryProtonationPhotochemistryMass spectrometryMethaneAnalytical ChemistryIonchemistry.chemical_compoundIonizationIsobutaneMoleculeSpectroscopySpectroscopyRapid Communications in Mass Spectrometry
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Synthesis and in vitro evaluation of galanthamine derivatives for examination of nicotinic acetylcholine receptor system

2001

ISunmrary: The syntheses and radioactive labeling of several galanthamine derivatives, 6-O-demethyl-6-O-fluoroethylgalanthamine, 10-N-demethyl-lO-Nfluoroethylgalanthamine and N-methylgalanthaminium are reported. First ill vitro evaluations were carried out to determine their properties as allosterically potentiating ligands of nicotinic receptors. N-methylgalanthaminium was found to be a promising candidate for further investigations. The most commonly applied therapeutic approach to balance nicotinic cholinergic deficits in Alzheimer’s disease (AD) patients is the administration of acetylcholinesterase inhibitors (AChE-I) although they have been proven to be of limited therapeutic value [ …

ChemistryOrganic ChemistryPharmacologyBiochemistryAnalytical ChemistryNicotinic acetylcholine receptorGanglion type nicotinic receptorNicotinic agonistBiochemistryDrug DiscoveryMuscarinic acetylcholine receptormedicineCholinergicRadiology Nuclear Medicine and imagingAlpha-4 beta-2 nicotinic receptorSpectroscopyAcetylcholineAcetylcholine receptormedicine.drugJournal of Labelled Compounds and Radiopharmaceuticals
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Pulsed photodissociation in an ion cyclotron resonance trap: extending the time range for unimolecular dissociation studies of metal clusters

1997

ChemistryOrganic ChemistryPhotodissociationAnalytical chemistryAtomic physicsTandem mass spectrometryTime rangeSpectroscopyFourier transform ion cyclotron resonanceDissociation (chemistry)Ion cyclotron resonanceAnalytical ChemistryMetal clustersRapid Communications in Mass Spectrometry
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