Search results for "liquid"

showing 10 items of 4351 documents

Synthesis, characterization and thermal properties of new aromatic quaternary ammonium bromides

2004

Series of new aromatic R 2R′ 2N +Br - (R=benzyl, 4-methylbenzyl, 2-phenylethyl, 3-phenylpropyl; R′=ethyl, methyl, isopropyl) or RR′ 2NH +Br --type (R=benzyl, R′=isopropyl) quaternary ammonium bromides were prepared by using novel synthetic route in which a formamide (N,N-diethylformamide, N,N-dimethylformamide, N,N-diisopropylformamide) is treated with aralkyl halide in presence of a weak base. The compounds were characterized by 1H-NMR and 13C-NMR spectroscopy and mass spectrometry. Structures of the crystalline compounds were determined by X-ray single crystal diffraction, and in addition the powder diffraction method was used to study the structural similarities between the single crysta…

FormamideAmmonium bromideInorganic chemistryTriclinic crystal systemIonic liquidCondensed Matter PhysicsQuaternary ammonium bromideElectronic Optical and Magnetic MaterialsInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryX-ray single crystal diffractionBromideX-ray powder diffractionIonic liquidMaterials ChemistryCeramics and CompositesOrthorhombic crystal systemThermal analysisPhysical and Theoretical ChemistryWeak interactionsIsopropylMonoclinic crystal systemJournal of Solid State Chemistry
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Chromatographically separable rotamers of an unhindered amide

2014

Surprisingly stable formamide rotamers were encountered in the tetrahydroisoquinoline and morphinan series of alkaloids. We investigated the hindered rotation around the amide bond by dynamic high-performance liquid chromatography (DHPLC) and kinetic measurements of the interconversion of the rotamers which can readily be separated by HPLC as well as TLC. The experimental results of the different methods were compared to each other as well as to results obtained by DFT calculations.

FormamideMorphinanTetrahydroisoquinolinedynamic HPLCOrganic ChemistryrotamersHigh-performance liquid chromatographyFull Research Paperamideslcsh:QD241-441Chemistrythermodynamicschemistry.chemical_compoundlcsh:Organic chemistrychemistryComputational chemistryAmidedensity functional calculationsOrganic chemistryPeptide bondlcsh:Qlcsh:ScienceConformational isomerismBeilstein Journal of Organic Chemistry
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Retention-pH profiles of acids and bases in hydrophilic interaction liquid chromatography

2018

Abstract The high proportion of acetonitrile used in many HILIC mobile phases significantly changes the acid-base properties of pH buffers and analytes foreseen from available data in water. In this paper, the recommended stability pH range for chromatographic columns is examined with various acetonitrile/water mixtures, resulting in a significant broadening in the operational pH window with the content of organic solvent. Additionally, the challenge of buffer selection in HILIC is also addressed. Commonly used ammonium acetate shrinks its pH buffering range in acetonitrile-rich mobile phases due to variations in the dissociation constants of the buffer constituents (acetic acid and ammoniu…

Formic acidOxalic acidHydrogen-ion concentrationLiquid chromatography02 engineering and technology01 natural sciencesBiochemistryCromatografia de líquidsAnalytical Chemistrychemistry.chemical_compoundAcetic acidSuccinimideEquilibri àcid-baseConcentració dels ions d'hidrogenEnvironmental ChemistryAcetonitrileTriethylamineSpectroscopyChromatographyHydrophilic interaction chromatography010401 analytical chemistry021001 nanoscience & nanotechnology0104 chemical sciencesAcid-base equilibriumchemistry0210 nano-technologyAmmonium acetate
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3,6-Bis(2-arylethenyl)-1,2,4,5-tetrazine - Synthese, Fl�ssigkristallinit�t und Photochemie

1995

3,6-Bis(2-arylethenyl)-1,2,4,5-tetrazines - Synthesis, LC Properties and Photochemistry The (E,E)-3,6-Bis(2-arylethenyl)-1,2,4,5-tetrazines 8 were prepared in a synthetic sequence starting with aromatic aldehydes 1 and cinnamic acids 2, respectively (Scheme 1). The rod-like conjugated molecules represent calamitic mesogens as well as extended chromophores. Hence, we investigated the formation of liquid crystals, achieved by the introduction of long flexible side chains, and the photochemical behaviour that is characterized by the fragmentation of the central ring (Scheme 3).

Fragmentation (mass spectrometry)Liquid crystalChemistryPolymer chemistrySide chainMoleculeSequence (biology)Conjugated systemChromophoreRing (chemistry)Journal f�r Praktische Chemie/Chemiker-Zeitung
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Article 40. Emoluments du liquidateur, Bénéfice du privilège général des frais de justice (non), Priorité de paiement de l'art. 40 (oui)

1998

International audience; (Com. 31 mars 1998, Mahieux ès qual. c/ Banque de Polynésie)

Frais de procédure[SHS.DROIT]Humanities and Social Sciences/LawPoursuite de l'activité[SHS.DROIT] Humanities and Social Sciences/LawREDRESSEMENT ET LIQUIDATION JUDICIAIRESPériode d'observationCréance prioritaire
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Studies on pathways of ring opening of benzene in a Fenton system

1995

Ring-opened products of benzene metabolism have been postulated to play a role in hematotoxicity and leukemogenesis. The reaction of benzene in the Fenton system was reexamined to determine the presence of compounds which might serve as intermediates in the formation of trans, trans-muconaldehyde (MUC), a microsomal hematotoxic metabolite of benzene. Benzene dihydrodiol (DHD) was found in this system based on coelution with authentic standard, ultraviolet (UV) absorption characteristics, and molecular weight. Incubation of DHD in the Fenton system resulted in the formation of phenol (PH), catechol (CAT), and products which reacted with thiobarbituric acid to form chromogens absorbing at 495…

Free RadicalsStereochemistryMetaboliteStereoisomerismIn Vitro TechniquesBiochemistryAldehydechemistry.chemical_compoundPhysiology (medical)AnimalsHumansPhenolBenzeneChromatography High Pressure LiquidCarcinogenchemistry.chemical_classificationAldehydesCatecholMolecular StructureHydroquinoneBenzeneStereoisomerismchemistrySpectrophotometryCarcinogensMicrosomes LiverFree Radical Biology and Medicine
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Drift velocity of free electrons in liquid argon

1999

Abstract A measurement of the drift velocity of free electrons in liquid argon has been performed. Free electrons have been produced by photoelectric effect using laser light in a so-called “laser chamber”. The results on the drift velocity vd are given as a function of the electric field strength in the range 0.5 kV / cm ⩽| E |⩽12.6 kV / cm and the temperature in the range 87 K ⩽T⩽94 K . A global parametrization of v d (| E |,T) has been fitted to the data. A temperature dependence of the electron drift velocity is observed, with a mean value of Δ v d /( Δ T v d )=(−1.72±0.08)%/ K in the range of 87–94 K.

Free electron modelPhysicsNuclear and High Energy PhysicsDrift velocityCalorimetryPhotoelectric effectLaserlaw.inventionlawElectric fieldLiquid argonDetectors and Experimental TechniquesAtomic physicsInstrumentationLaser lightNuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment
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Supported Fullerene C60-Ionic Liquid Hybryds as New Catalytic Materials

2015

Fullerene C60 Ionic Liquids Catalysis Suzuki reactionSettore CHIM/06 - Chimica Organica
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Nuovi ibridi [60]fullerene-liquido ionico

2014

Fullerene liquidi ionici reazione di Suzuki
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Catalytic Synergism in a C60IL10TEMPO2 Hybrid in the Efficient Oxidation of Alcohols

2014

A novel fullerene (5:1)hexakisadduct bearing two 2,2,6,6-tetramethylpiperidine 1-oxyl (TEMPO) radicals and ten 1-propyl-3-methylimida- zolium bromide moieties has been synthesized and characterized. Such an C60IL10TEMPO2 hybrid has been successfully employed as a catalyst in the se- lective oxidation of a wide series of alcohols and is highly active at just 0.1 mol% loading. Moreover, it can be easily recovered by adsorption onto a multi- layered covalently-linked SILP phase (mlc-SILP) through a "release and catch" approach and reused for up to 12 cycles without loss in efficiency. Inter- estingly, a catalytic synergistic effect of TEMPO and imidazolium bromide moieties combined in the same…

FullereneChemistryalcoholoxidationRadicalfullereneGeneral ChemistrySettore CHIM/06 - Chimica OrganicaCombinatorial chemistryCatalysischemistry.chemical_compoundAdsorptionBromidePhase (matter)Alcohol oxidationOrganic chemistry2266-tetramethylpiperidine 1-oxyl (TEMPO)ionic liquid
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