Search results for "Azine"

showing 10 items of 1589 documents

On the synthesis and characterization of layered antimony(III) phosphate and its interaction with moist ammonia and amines

1998

Samples of antimony(III) phosphate, a layered material, were prepared at room temperature, using the two allotropic forms of Sb2O3, layered valentinite and cubic senarmontite. The compounds were characterized by infrared spectroscopy, X-ray diffraction, and thermogravimetric–differential thermal analysis. Solids exposed to ammonia, ethylenediamine, or hydrazine vapors also were studied. The interaction between SbPO4 and the bases always led to the formation of stoichiometric amounts of Sb2O3 and hydrogen phosphate(–2) salts of the bases. With ammonia, the SbPO4 raw materials gave rise to valentinite or senarmontite, depending on which Sb2O3 allotropic form was used to prepare antimony phosp…

ChemistryMechanical EngineeringInorganic chemistryHydrazineIntercalation (chemistry)Infrared spectroscopychemistry.chemical_elementEthylenediamineCondensed Matter PhysicsPhosphateThermogravimetrychemistry.chemical_compoundAntimonyMechanics of MaterialsDifferential thermal analysisGeneral Materials ScienceMaterials Research Bulletin
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Radical cations and dications of bis[1]benzothieno[1,4]thiazine isomers

2021

Bis[1]benzothieno[1,4]thiazines (BBTT) are particularly electron-rich S,N-heteropentacenes and their radical cations and dications can be relevant intermediates in charge transport materials. All three regioisomers of N-p-fluorophenyl-BBTT (syn–syn, syn–anti, and anti–anti) were studied. A reliable preparation of radical cations and dications using antimony pentachloride as an oxidant gives deeply colored salts. The electronic structure of the radical cations was assessed by EPR spectroscopy, whereas dicationic structures were characterized by NMR spectroscopy. In addition, a deeper insight into the electronic structure was experimentally and computationally obtained by UV/Vis spectroscopy …

ChemistryOrganic ChemistryAntimony pentachlorideCationic polymerizationNuclear magnetic resonance spectroscopyTime-dependent density functional theoryPhotochemistrylaw.inventionchemistry.chemical_compoundlawThiazineStructural isomerElectron paramagnetic resonanceSpectroscopyOrganic Chemistry Frontiers
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Effect of Experimental and Sample Factors on Dehydration Kinetics of Mildronate Dihydrate: Mechanism of Dehydration and Determination of Kinetic Para…

2014

The dehydration kinetics of mildronate dihydrate [3-(1,1,1-trimethylhydrazin-1-ium-2-yl)propionate dihydrate] was analyzed in isothermal and nonisothermal modes. The particle size, sample preparation and storage, sample weight, nitrogen flow rate, relative humidity, and sample history were varied in order to evaluate the effect of these factors and to more accurately interpret the data obtained from such analysis. It was determined that comparable kinetic parameters can be obtained in both isothermal and nonisothermal mode. However, dehydration activation energy values obtained in nonisothermal mode showed variation with conversion degree because of different rate-limiting step energy at hi…

ChemistrySAMPLE historyKineticsWaterPharmaceutical ScienceThermodynamicsCardiovascular AgentsActivation energyKinetic energymedicine.diseaseIsothermal processKineticsmedicineSample preparationParticle sizeDehydrationParticle SizeMethylhydrazinesJournal of Pharmaceutical Sciences
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Hydrogen bond-stabilised N-alkylammonium resorcinarene halide cavitands

2010

A family of hydrogen bond-stabilised N-alkylammonium resorcinarene chloride and bromide cavitands were synthesised and characterised with 1H NMR and ESI mass spectrometry. The seven compounds exhibit interestingly either self-inclusion or guest complexation in the solid state evidenced by single crystal X-ray diffraction. The four dimers show self-inclusion of the upper rim propyl chains and consist of two hydrogen-bonded resorcinarene tetracations and six halide anions, while the remaining two halide anions are located in between the dimers linking them via hydrogen bonding. Small solvent molecules such as dichloromethane, methanol, n-butanol or chloroform are complexed into the resorcinar…

ChloroformHydrogen bondHalideGeneral ChemistryResorcinarenePhotochemistrySolventchemistry.chemical_compoundchemistryBromidePolymer chemistryProton NMRMoleculeresorcinarenes; tetrabenzoxazines; ammonium halides; hydrogen bonding; X-ray structure
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Lichen microalgae are sensitive to environmental concentrations of atrazine

2017

The identification of new organisms for environmental toxicology bioassays is currently a priority, since these tools are strongly limited by the ecological relevance of taxa used to study global change. Lichens are sensitive bioindicators of air quality and their microalgae are an untapped source for new low-cost miniaturized bioassays with ecological importance. In order to increase the availability of a wider range of taxa for bioassays, the sensitivity of two symbiotic lichen microalgae, Asterochloris erici and Trebouxia sp. TR9, to atrazine was evaluated. To achieve this goal, axenic cultures of these phycobionts in suspension were exposed to a range of environmental concentrations of …

Chlorophyll0301 basic medicineTrebouxiaLichensPopulation010501 environmental sciencesBiologyEcotoxicology01 natural sciences03 medical and health scienceschemistry.chemical_compoundChlorophytaBotanyMicroalgaeEcotoxicologyAtrazineSymbiosiseducationAxenic0105 earth and related environmental scienceseducation.field_of_studyDose-Response Relationship DrugGeneral Medicinebiology.organism_classificationPollution030104 developmental biologychemistryEnvironmental toxicologyAtrazineEcotoxicityBioindicatorWater Pollutants ChemicalFood ScienceJournal of Environmental Science and Health, Part B
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Hierarchical Self-Organization of Perylene Bisimide–Melamine Assemblies to Fluorescent Mesoscopic Superstructures

2000

A series of three perylene tetracarboxylic acid bisimide dyes 3a-c bearing phenoxy substituents at the four bay positions of the perylene core were synthesized and their complexation behavior to complementary ditopic dialkyl melamines 8a-c was investigated. Binding constants and Gibbs binding energies for the hydrogen bonds between the imide and the complementary melamine moiety have been determined in several solvents by NMR and UV/Vis titration experiments with monotopic model compounds 5 and 9. The effects of the solvent polarity and specific solvent-solute interactions on the degree of polymerization of (3 x 8)n are discussed, and a general formula to estimate the chain length of [AA-BB…

ChlorophyllMagnetic Resonance SpectroscopyLightPolymersMolecular ConformationSupramolecular chemistryDegree of polymerizationImidesPhotochemistryFluorescenceCatalysischemistry.chemical_compoundNon-covalent interactionsPerylenechemistry.chemical_classificationMicroscopy ConfocalTriazinesHydrogen bondOrganic ChemistryOptical polarizationPolymerGeneral ChemistrySolutionsSupramolecular polymersMicroscopy ElectronchemistrySpectrophotometry UltravioletPeryleneChemistry – A European Journal
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Performance of micellar mobile phases in reversed-phase chromatography for the analysis of pharmaceuticals containing beta-blockers and other antihyp…

1996

A rapid and simple reversed-phase micellar liquid chromatographic procedure for the simultaneous determination of the beta-blockers atenolol, metoprolol and oxprenolol, the diuretics amiloride, bendroflumethiazide, chlorthalidone and hydrochlorothiazide and the vasodilator hydralazine in pharmaceuticals, is proposed. An interpretive optimization procedure, which uses the chromatographic data for only five mobile phases, was applied to select a suitable micellar mobile phase. A comparative study was also made of the performance of micellar and aqueous-organic mobile phases in the analysis of pharmaceuticals that combine beta-blockers and diuretics. The determination of all the drugs could be…

ChromatographyAdrenergic beta-AntagonistsReversed-phase chromatographyAtenololHydralazineBiochemistryHigh-performance liquid chromatographyDosage formAnalytical Chemistrychemistry.chemical_compoundHydrochlorothiazidechemistryOxprenololElectrochemistrymedicineSolventsEnvironmental ChemistryBendroflumethiazideSodium dodecyl sulfateDiureticsSpectroscopyAntihypertensive AgentsChromatography High Pressure LiquidMicellesmedicine.drugThe Analyst
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Photochemical Derivatization and Fluorimetric Determination of Promethazine in a FIA Assembly

1992

Abstract The flow injection fluorimetric determination of promethazine is carried out by on-line photoderivatization. The PTFE tubing is helically coiled around the lamp. An analytical procedure is proposed by using aqueous solution as carrier stream: the calibration graph is linear over the range 0.05 - 20 ppm. The influence of foreign compounds is studied and the method is applied to promethazine determination in pharmaceutical formulations.

ChromatographyAqueous solutionCalibration curveBiochemistry (medical)Clinical BiochemistryBiochemistryDosage formFluorescence spectroscopyAnalytical ChemistryPromethazinechemistry.chemical_compoundchemistryElectrochemistrymedicineDerivatizationSpectroscopymedicine.drugAnalytical Letters
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Influence of template basicity and hydrophobicity on the molecular recognition properties of molecularly imprinted polymers

1996

Abstract Triazine herbicides were used as model templates for a basic study of the molecular recognition process in imprinted polymers. Five structurally related triazine herbicides (atrazine, ametryn, cyanazine, prometryn and terbutylazine) that differ in basicity and hydrophobicity were imprinted. Chromatographic evaluation of the resulting materials in an aqueous-poor mobile phase showed that the selectivity for the template increased with its Bronsted basicity whereas it did not correlate with template hydrophobicity. Thus, the highest and lowest affinity and selectivity for the template was observed using the ametryn-imprinted (p K a =4.1) and the cyanazine-imprinted polymers (p K a =1…

ChromatographyAqueous solutionOrganic ChemistryMolecularly imprinted polymerGeneral MedicineBiochemistryAnalytical ChemistryGel permeation chromatographyPartition coefficientchemistry.chemical_compoundMolecular recognitionchemistryPolymer chemistryMolecular imprintingSelectivityTriazineJournal of Chromatography A
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Univariate method for background correction in liquid chromatography–Fourier transform infrared spectrometry

2007

An univariate method is proposed for background correction in on-line gradient liquid chromatography-Fourier transform infrared (LC-FTIR) spectrometry using acetonitrile:water as mobile phase components. The method is based on the calculation of the ratio of absorbances (AR) at two characteristic wavenumbers for each spectrum. This parameter is subsequently used to locate the most appropriated eluent spectrum within a reference spectra matrix (RSM) to be subtracted from each spectrum included in the sample chromatogram. To correct minor changes in eluent spectra intensity during the elution of analytes, a correction factor (Kf), defined as the ratio of the absorbance of the sample and the s…

ChromatographyChemistryElutionOrganic ChemistryAnalytical chemistryInfrared spectroscopyGeneral MedicineReference StandardsMass spectrometryBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryMatrix (chemical analysis)ChemometricsAbsorbanceDiuronSpectroscopy Fourier Transform InfraredAtrazineFourier transform infrared spectroscopyChromatography LiquidJournal of Chromatography A
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