Search results for "Perchloric acid"

showing 10 items of 19 documents

A joint experimental and ab initio study on the reactivity of several hydroxy selenides. Stereoselective synthesis of cis-disubstituted tetrahydrofur…

2001

Abstract The reactivity of several hydroxy selenides bearing an ethereal chain with catalytic amounts of perchloric acid in dichloromethane was investigated. Results showed that the position of the oxygen atom with respect to the seleniranium ring was crucial in order to get a good yield of the cyclized product. The factors on which yields of the 5- endo cyclization of the seleniranium ions depend were analysed by ab initio (HF/3-21G ∗ ) studies. An explanation of the different coordinating ability, towards the positively charged selenium atom, of the allylic OMe and homoallylic OH-2 groups was given.

Allylic rearrangementStereochemistryOrganic ChemistryAb initioBiochemistryMedicinal chemistryCatalysischemistry.chemical_compoundchemistrycyclizations oxygen heterocycles selenium theoretical studiesYield (chemistry)Drug DiscoveryReactivity (chemistry)StereoselectivityPerchloric acidDichloromethane
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Determination of tannic acid by direct chemiluminescence in a FIA assembly

2002

The determination of tannic acid is performed in a FIA assembly on the basis of the analytical output obtained by oxidation of the acid. The analyte solution was daily prepared in a mixture of quinine as sensitiser and perchloric acid and it was injected into a pure water stream acting as a carrier. This solution merges with the mixture potassium permanganate in perchloric medium and the resulting chemiluminescence is monitored. The method was applied over the range 0.5-20 mg l(-1) of tannic acid with a LOD 100 mug l(-1). The reproducibility was 2.1% and the sample throughput 54 h(-1). The influence of foreign substances was studied and the new method is applied to the determination of tann…

AnalyteChromatographyDosage formAnalytical Chemistrylaw.inventionchemistry.chemical_compoundPotassium permanganatechemistrylawTannic acidPhenolsPerchloric acidQuantitative analysis (chemistry)ChemiluminescenceTalanta
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Thermodynamic parameters of the interaction between Co(II) bovine carbonic anhydrase and anionic inhibitors

1992

The pH dependence of the apparent affinity constants of perchlorate for cobalt(II)bovine carbonic anhydrase II has been measured by electronic absorption spectroscopy. The obtained data have been analyzed in terms of the ionization of two acidic groups of CoBCAII, and the affinity of perchlorate for the two water-containing species of the enzyme have been estimated. Furthermore, the affinity constants of nitrate, perchlorate, and azide for CoBCAII in the temperature range 5 degrees C-30 degrees C have been determined by spectrophotometric titrations at pH 7. The affinity constants for these ligands decrease with increasing temperatures. The temperature dependence of binding was used to esti…

AnionsAzidesCarbonic anhydrase IIEnthalpyInorganic chemistrychemistry.chemical_elementBiochemistryInorganic Chemistrychemistry.chemical_compoundPerchlorateCarbonic anhydraseAnimalsPerchloric acidCarbonic Anhydrase InhibitorsCarbonic AnhydrasesNitratesPerchloratesbiologyCobaltKineticschemistrySpectrophotometrybiology.proteinThermodynamicsCattleTitrationAzideCobaltMathematicsJournal of Inorganic Biochemistry
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Kinetics of the permanganate oxidation of formic acid in aqueous solution

1987

The kinetics of the permanganate oxidation of formic acid in aqueous perchloric acid at 30°C were examined by the spectrophotometric method. The chemical reaction 2MnO + 3HCOOH + 2H+ 2MnO2 + 3CO2 + 4H2O, appears to proceed via several parallel reactions. The overall rate equation has been obtained by using statistical multilinear regression analysis of the 660 cases studied, and the presence in the rate equation of two new terms in relation to previous studies shows that both permanganate autocatalytic effects and acid media inhibition must be taken into account when the reaction proceeds at constant ionic strength.

Aqueous solutionFormic acidOrganic ChemistryPermanganateInorganic chemistryRate equationBiochemistryChemical reactionInorganic ChemistryAutocatalysischemistry.chemical_compoundchemistryIonic strengthPerchloric acidPhysical and Theoretical ChemistryInternational Journal of Chemical Kinetics
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Determination of biogenic amines in meat by combined ion-exchange capillary gas chromatography

1984

Abstract A procedure is described for the determination of putrescine, cadaverine and histamine in meat. Crude perchloric acid extracts were pre-separated on a weakly acidic cation exchanger and the amines quantified by capillary gas chromatography. The diamines were analysed as trifluoroacetyl derivatives and histamine was converted into N α -trifluoroacetyl-N τ -ethoxycarbonylhistamine. The accuracy of the determination of diamines was examined by a precipitation pre-separation method and by mass fragmentometric quantification. The proposed procedure allows the sensitive, sufficiently precise and highly specific determination of putrescine and cadaverine in meat.

Biogenic AminesChromatography GasMeatSwineTetraphenylborateBiochemistryGas Chromatography-Mass SpectrometryAnalytical Chemistrychemistry.chemical_compoundCadaverinePutrescineAnimalsChemical PrecipitationTrifluoroacetic AcidPerchloric acidCadaverineChromatographyIon exchangePrecipitation (chemistry)Organic ChemistryGeneral MedicineChromatography Ion ExchangeCapillary gas chromatographychemistryPutrescineHistamineHistamineJournal of Chromatography A
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Laser depassivation of a channel flow double-electrode: A new technique in repassivation studies

1993

Abstract A powerful tool for distinguishing between the different electrochemical steps involved during a depassivation-repassivation sequence was developed by combining the pulsed laser depassivation technique with an hydrodynamic electrochemical method: the channel flow double-electrode (CFDE). This experiment consisted of transporting the chemical species (Fe 2+ ) released by a depassivated iron electrode to a collecting electrode where these species were oxidized. A qualitative idea of the relative contribution of the anodic dissolution to the repassivation behavior was obtained. For a passive iron in acidic solution it was found that about 15% of the total charge is related to anodic d…

General Chemical EngineeringMetallurgyInorganic chemistryGeneral ChemistryLaserElectrochemistryCorrosionOpen-channel flowlaw.inventionchemistry.chemical_compoundChemical specieschemistrylawElectrodeGeneral Materials ScienceAnodic dissolutionPerchloric acidCorrosion Science
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Initiatoren für die polymerisation des trioxane. 20. Mitt. über polyoxymethylene1

1963

Die Polymerisation des Trioxans bei 60°C in Cyclohexan mit verschiedenen kationischen Initiatoren wurde untersucht. Die aktivsten Initiatoren sind Acetylperchlorat, Perchlorsaure, FeCl3 und SnCl4. Die Molekulargewichte der erhaltenen Polyoxymethylene sind bei den aktivsten Initiatoren am hochsten. Der Einflus der ubertragung durch Wasser und der kinetischen Kettenlange auf die Molekulargewichte wird diskutiert. Wahrend der Polymerisation kann durch den Initiator eine Spaltung bereits gebildeter Makromolekule erfolgen, welche die Molekulargewichte stark reduziert. Die Frage der Cokatalyse bei der kationischen Polymerisation des Trioxans mit Ansolvosauren wurde untersucht. Bei der Polymerisat…

Kinetic chain lengthPerchloratechemistry.chemical_compoundchemistryPolymerizationCyclohexaneTrioxanePolymer chemistryCationic polymerizationLewis acids and basesPerchloric acidDie Makromolekulare Chemie
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GAS CHROMATOGRAPHIC ESTIMATION OF ACETYLCHOLINE IN THE RABBIT HEART USING A NITROGEN SELECTIVE DETECTOR

1973

The distribution of ACh in the rabbit heart was investigated by a modified gas chromatographic estimation method. ACh was extracted with perchloric acid, precipitated as reineckate and demethylated with sodium benzenethiolate. The tertiary amines derived from ACh and other choline esters were concentrated by a microdistillation procedure. Gas chromatography was performed using a nitrogen selective detector. In the range of concentrations between 0.4 and 2.5 nmol ACh per tissue sample the coefficient of variation was 5.2 per cent. The recovery of ACh added to heart extracts was 101 per cent. Evidence for the identity of the choline ester isolated from rabbit hearts and authentic ACh was obta…

MaleChromatography GasHeart VentriclesCoefficient of variationSodiumchemistry.chemical_elementBlood PressureBiochemistryCholineCellular and Molecular Neurosciencechemistry.chemical_compoundMethodsmedicineAnimalsBioassayCholineHeart AtriaPerchloric acidButyrylcholineChromatographyChemistryMyocardiumAcetylcholineRatsButyratesBiological AssayFemaleRabbitsGas chromatographyPropionatesAcetylcholinemedicine.drugJournal of Neurochemistry
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A tensiostatic study of the anodic behaviour of tungsten in acid solutions

1975

Abstract Tensiostatic anodization of tungsten has been studied in 1 N solutions of H 2 SO 4 , HClO 42 , HNH 2 SO 3 and HCl at 25 °C. For several voltage values, the curves of current vs . time and open-circuit voltage vs . time have been obtained. All results indicate that the oxide films produced during the polarization are slowly dissolved in the acid solutions. The HCl, and to a lesser extent the HNH 2 SO 3 solutions, show a more aggressive behaviour. For values of the applied voltage above about 50 V, gas evolution begins. In the case of HCl solutions, the gas is Cl 2 and the electrode is rapidly corroded.

Materials scienceAqueous solutionGas evolution reactionInorganic chemistryGeneral EngineeringOxidechemistry.chemical_elementSulfuric acidHydrochloric acidTungstenchemistry.chemical_compoundchemistryElectrodePerchloric acidJournal of the Less Common Metals
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Dehydrogenation versus Oxygenation in Two-Electron and Four-Electron Reduction of Dioxygen by 9-Alkyl-10-methyl-9,10-dihydroacridines Catalyzed by Mo…

2004

Dehydrogenation of 10-methyl-9,10-dihydroacridine (AcrH(2)) by dioxygen (O(2)) proceeds efficiently, accompanied by the two-electron and four-electron reduction of O(2) to produce H(2)O(2) and H(2)O, which are effectively catalyzed by monomeric cobalt porphyrins and cofacial dicobalt porphyrins in the presence of perchloric acid (HClO(4)) in acetonitrile (MeCN) and benzonitrile (PhCN), respectively. The cobalt porphyrin catalyzed two-electron reduction of O(2) also occurs efficiently by 9-alkyl-10-methyl-9,10-dihydroacridines (AcrHR; R = Me, Et, and CH(2)COOEt) to yield 9-alkyl-10-methylacridinium ion (AcrR+) and H(2)O(2). In the case of R = Bu(t) and CMe(2)COOMe, however, the catalytic two…

Metalloporphyrinschemistry.chemical_elementElectronsReaction intermediatePhotochemistryBiochemistryMedicinal chemistryCatalysisCatalysischemistry.chemical_compoundColloid and Surface ChemistryDehydrogenationPerchloric acidAlkylchemistry.chemical_classificationPerchloratesChemistryCobaltGeneral ChemistryNADPorphyrinKineticsBenzonitrileAcridinesHydrogenationOxidation-ReductionCobaltJournal of the American Chemical Society
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