Search results for "Chlorobenzene"

showing 10 items of 104 documents

Zur Autoxydation von Polystyrol

1971

Die mit Azoisobuttersauredinitril (AIBN) initiierte Autoxydation von Polystyrol (PS) in Chlorbenzol bei 60°C ist von der Ordnung 0,75, bezogen auf AIBN, und 0,34, bezogen auf PS. Der niedrige Exponent der Polystyrolkonzentration weist neben intermolekularen Wachstumsschritten auf intramolekulare Reaktionsschritte bei der Autoxydation hin. Die bei der Autoxydation am Polystyrol gebildeten Hydroperoxidgruppen zerfallen in Essigsathylester als Losungsmittel mit einer Aktivierungsenthalpie von 19,7 kcal/Mol und einer Aktivierungsentropie von −29 cal/Mol Grad. Das spricht fur einen monomolekularen bifunktionellen Zerfallsmechanismus. Als fluchtige Produkte bei diesem Hydroperoxidzerfall werden P…

BenzaldehydeSolventchemistry.chemical_compoundchemistryChlorobenzenePolymer chemistryEnthalpyPhenolPolystyreneBifunctionalAcetophenoneDie Makromolekulare Chemie
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A CNDO/2 study on the additivity and the nature of the non-additivity of the substituent effects on13C NMR shifts in chlorobenzenes and chlorophenols

1980

The general correlation between the electron densities and the 13C NMR chemical shifts is found to be quite poor in the cases discussed. The non-additivities of the substituent effects on the chemical shifts and the CNDO/2 electron densities correlate only weakly. However, when the electron densities are made specific to different types of atomic orbitals, the s electrons have a pronounced effect in all the models tested. This is explained by an indirect effect on the 〈1/r3〉 term of the p electrons. Good correlations are found between the sums of the chemical shifts and the corresponding sums of the substituent charge excesses. The different behaviour of OH and Cl substituents in the additi…

CNDO/2chemistry.chemical_compoundAtomic orbitalComputational chemistryChemistryChlorobenzeneChemical shiftAdditive functionSubstituentGeneral Materials ScienceGeneral ChemistryElectronCarbon-13 NMROrganic Magnetic Resonance
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Gas—liquid chromatographic analyses

1984

Abstract The gas chromatography (GC) of n -alkyl acetates (CH 3 COOR), chloroacetates (CH 2 ClCOOR), dichloroacetates (CHCl 2 COOR) and trichloroacetates (CCl 3 COOR), where the alcohol chain length (R) varied between 1 and 8, and certain of their monochlorinated derivatives, 176 compounds altogether, has been studied on SE-30 and OV-351 glass capillary columns under the same operating conditions. The isomeric monochlorinated esters are eluted in direct order from the 1- chloro to the ω-chloro isomer, the separation of the isomers being complete on OV- 351. On SE-30, however, the peaks of the 6- and 7-chlorooctyl esters are partly overlapped. The separation of the mixtures of odd- and e…

Capillary actionAnalytical chemistryAlcoholFormyl groupAldehydeBiochemistryAnalytical Chemistrychemistry.chemical_compoundCapillary columnStraight chainpolycyclic compoundsStructural isomerOrganic chemistryMethyleneBenzoic acidchemistry.chemical_classificationPrimary (chemistry)General MedicineCapillary gas chromatographyBoiling pointChromatographic separationSalicylaldehydeNitrobenzoatesPolarlipids (amino acids peptides and proteins)Aliphatic compoundResolution (mass spectrometry)Polarity (physics)Carboxylic acidchemistry.chemical_elementBranching (polymer chemistry)Isothermal processTurn (biochemistry)ChlorinePhenolsQuartzAlkylTetradecaneChlorophenolDegree of unsaturationChromatographyGeminalElutionOrganic ChemistryChloroacetatesComplete resolutionReverse orderChain lengthchemistryChlorobenzeneFunctional groupNitroKovats retention indexNon polarGas chromatographyVicinalGas liquid chromatographicJournal of Chromatography A
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Relations between compression and thermal contraction in 1,2,4-trichlorobenzene and melting of trichlorobenzene isomers

2015

The compression and thermal expansion of crystalline 1,2,4-trichlorobenzene, C6H3Cl3, 124TCB, investigated under isobaric and isothermal conditions, are in reverse relation, as for most of crystals, however, the isochoric strain along direction c is clearly different from those along a and b. Single crystals of 124TCB have been in situ grown under isochoric and isobaric conditions, at 270 K/0.1 MPa and 295 K/0.16 GPa, and also at 100 K/0.1 MPa and 295 K/0.64 GPa, when the unit-cell volume is similar. All crystallizations yielded the same phase, of monoclinic space group P21/n, with two symmetry-independent molecules (Z′ = 2). The structure is governed by Cl⋯Cl and Cl⋯H interactions and the …

ChemistryIsochoric processThermodynamicsTrichlorobenzeneGeneral ChemistryCondensed Matter PhysicsThermal expansionIsothermal processPhase (matter)medicineIsobaric processGeneral Materials Sciencemedicine.drugPhase diagramMonoclinic crystal systemCrystEngComm
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Conductance in isodielectric mixtures. III.i-butyronitrile with chlorobenzene,o-dichlorobenzene,p-dichlorobenzene, 1,2-dichloroethane, andn-pentanol

1975

The conductance of tetrabutylammonium tetraphenylboride, picrate, perchlorate, and nitrate has been measured at 25°C in mixtures ofi-butyronitrile with chlorobenzene,o-dichlorobenzene,p-dicholorobenzene, 1,2-dichloroethane, andn-pentanol covering the range of dielectric constants 10≤D≤20. In these mixtures of polar solvents, both association constants and ionic mobilities depend on ion-solvent interaction energies and on free volume in a manner that is specific for each system. This failure of the primitive model (rigid charged spheres in a continuum) is shown to be the consequence of short-range spatial and energetic interactions between ions and adjacent solvent molecules.

ChemistryPicrateInorganic chemistryBiophysicsConductanceIonic bonding12-DichloroethaneBiochemistrySolventchemistry.chemical_compoundPerchlorateChlorobenzeneButyronitrilePhysical chemistryPhysical and Theoretical ChemistryMolecular BiologyJournal of Solution Chemistry
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A statistical study of the additivities of substituent effects in the13C NMR chemical shifts of hydroxy- and chloro-substituted benzenes

1980

The 13C NMR spectra of six hydroxybenzenes, all chlorobenzenes, all chlorophenols and eight chlorocatechols are measured and assigned. The additivity of the substituent effects and the usefulness of some corrective parameters are studied with regression analysis. The order of the chemical shifts is most efficiently predicted by the simplest substituent effect model, containing only the direct effects of the substituents, although the 95% confidence limits of the calculated shifts are as high as 5.6 ppm. If the chemical shifts need to be predicted within the measuring errors (approximately 0.05–0.10 ppm, in the present data), the number of necessary corrections is very impractical. The corre…

ChemistryStereochemistryChemical shiftDirect effectsSubstituentGeneral ChemistryCarbon-13 NMRSpectral lineSolventchemistry.chemical_compoundChlorobenzeneComputational chemistryAdditive functionGeneral Materials ScienceOrganic Magnetic Resonance
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Determination of organochlorine pesticide residues in honey from the central zone of Portugal and the Valencian community of Spain

2004

In this study nine organochlorine pesticide residues ([alpha]-, [beta]-, and [gamma]-hexachlorocyclohexane (HCH), hexachlorobenzene (HCB), aldrin, p,p'-DDE, p,p'-DDD, o,p'-DDT, and p,p'-DDT) in forty nine samples of honey collected from markets of Portugal and Spain during 2001 and 2002, respectively, were evaluated. For this evaluation, three analytical procedures were studied. The analytical procedure, based on LLE extraction with ethyl acetate followed by gas chromatography-electron-capture detection (GC-ECD) for quantification, and mass spectrometry (GC-MS) for confirmation, has been selected. Recoveries of spiked samples ranged from 68%, for [beta]-HCH, and 126% for p,p'-DDT, for forti…

Chromatography GasEthyl acetateOrganochlorineBiochemistryGas Chromatography-Mass SpectrometryAnalytical Chemistrychemistry.chemical_compoundElectrochemistryHydrocarbons ChlorinatedAldrinForty NinePesticidesDetection limitChromatographyPortugalPesticide residueOrganic ChemistryPesticide ResiduesReproducibility of ResultsHoneyGeneral MedicineHexachlorobenzeneReference StandardsPesticidechemistrySpainGas chromatography–mass spectrometryJournal of Chromatography A
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Glass-capillary gas chromatography of chlorobenzenes on SE-30 and Carbowax 20M columns. Simultaneous determination of chlorobenzenes and chlorophenols

1983

Gas chromatography of benzene and all chlorobenzenes has been studied on SE-30 and Carbowax 20M glasscapillary columns under various operating conditions. The benzene isomers are eluted on both columns according to their boiling points. Separation of all components in a mixture is achieved on Carbowax 20M, whereas on SE-30 the peaks of closely related isomers overlapped. Also one partial overlapping is observed on a non-polar phase. The relative retention times for compounds are given and the retention order is discussed. The retention behaviour of chlorobenzenes and chlorophenols is compared. By using an SE-30 quartz-capillary column a mixture of 33 individual components gives 29 resolved …

ChromatographyChemistryElutionOrganic ChemistryClinical BiochemistryAnalytical chemistryBiochemistryCapillary gas chromatographyAnalytical ChemistryBoiling pointchemistry.chemical_compoundChlorinated phenolsChlorobenzenePhase (matter)Gas chromatographyBenzeneChromatographia
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Retention increments of isomeric chlorobenzenes

1983

The chlorobenzene isomers are used extensively as intermediates in a wide range of chemical products. More recently their determination in environmental situations has become of considerable importance and chromatographic procedures have been widely reported for their determination in both trace and major amounts. There are over 220 publications in which gas chromatography (GC) has been applied to the analysis of chlorobenzene. However, over 60 o/o of these works refer to the separation of only one isomer. Relatively few publications’-8 consider all the isomers, although the use of both capillary3’ and packedcolumns with polar and non-polar stationary phases has been reported. Temperature p…

ChromatographyElutionOrganic Chemistrychemistry.chemical_elementGeneral MedicineBiochemistryIsothermal processAnalytical Chemistrychemistry.chemical_compoundchemistryChlorobenzeneChemical productsChlorineKovats retention indexPolarGas chromatographyJournal of Chromatography A
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Permeability and toxicological profile estimation of organochlorine compounds by biopartitioning micellar chromatography

2008

This paper points out the usefulness of biopartitioning micellar chromatography (BMC) as a high-throughput primary screening tool providing key information about the oral absorption, skin permeability (Kp), brain–blood distribution coefficient (BB) and ecotoxicological parameters such as median lethal concentration (LC50) and bioconcentration factors of 15 organochloride compounds. The retention data of compounds in BMC conditions were interpolated in previously developed quantitative–retention activity relationships by our research group. Results show that the compounds studied readily cross the intestinal barrier (oral absorption >ercnt;) and the blood–brain barrier (log BB >p;0.4). In ad…

Clinical BiochemistryBioconcentrationAbsorption (skin)Models BiologicalBiochemistryPermeabilityAnalytical Chemistrychemistry.chemical_compoundDrug DiscoveryHydrocarbons ChlorinatedAnimalsHumansDicofolPesticidesMolecular BiologySkinPharmacologyChromatographyChromatographyGeneral MedicineHexachlorobenzeneOrganochlorideBioavailabilityPartition coefficientchemistryBlood-Brain BarrierChlorobenzeneEnvironmental chemistrySoftwareBiomedical Chromatography
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