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  • 1
    ISSN: 1437-1596
    Keywords: Phencyclidine ; Pethidine ; Gas chromatography ; Surface ionization detection ; Sep-Pak C18 cartridges
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine , Law
    Notes: Abstract Phencyclidine (PCP) can be detected in body fluids with very high sensitivity by gas chromatography (GC) with surface ionization detection (SID) using pethidine as internal standard. PCP was extracted with Sep-Pak C18 cartridges from whole blood and urine samples, which gave clean extracts. The calibration curve for spiked whole blood was linear in the range 1.25–20 ng/ml. The detection limit of PCP was approximately 15 pg on-column (0.75 ng/ml sample), which was much lower than by GC-nitrogen phosphorus detection. The recovery of PCP and pethidine from spiked whole blood or urine samples was above 85%. This method seems very useful for the determination of PCP in forensic and clinical toxicology.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 179 (1996), S. 331-344 
    ISSN: 1432-1351
    Keywords: Hylobius abietis ; Olfaction ; Plant odours ; Receptor neuron responses ; Gas chromatography ; Electrophysiology
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Receptor neuron responses to plant volatiles, trapped by head-space procedures, were examined in the pine weevil Hylobius abietis, using gas chromatography linked with electrophysiological recordings from single neurons. Seventy-two receptor neurons were tested 173 times for various plant volatile mixtures, either via a polar or a non-polar column. 1) All responses appeared as increased firing rates which followed the concentration profiles of the GC-eluted compounds. 2) The neurons were classified separately for the two column types in 17 and 19 groups respectively, according to the compounds they responded to. It suggests that the plant odour information is encoded by a large, but limited number of receptor neuron types. 3) Most neurons responded to a limited number of compounds (1–5) and showed a marked best response to one of them, whereas additional responses to several other components which seems to be structurally similar, was recorded for some neurons. It suggests that the plant odour receptor neurons are rather narrowly than broadly tuned, and that each neuron is specialized for receiving information about one or a few related compounds. 4) Most neurons responded to monoterpenes, whereas the other neurons responded to compounds of other categories. 5) Both major and minor plant volatile components activated specifically receptor neurons.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    International archives of occupational and environmental health 68 (1996), S. 262-267 
    ISSN: 1432-1246
    Keywords: Gas chromatography ; Mass spectrometry ; Benzene ; Air pollution
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract There is no shortage of information about the average benzene concentrations in urban air, but there is very little about microenvironmental exposure, such as in-vehicle concentrations while driving in various traffic conditions, while refuelling, or while in a parking garage. The main reason for this lack of data is that no analytical instrumentation has been available to measure on-line trace amounts of benzene in such situations. We have recently proposed a highly accurate, high-speed cryofocusing gas chromatography/mass spectrometry (GC/MS) system for monitoring benzene concentrations in air. Accuracy of the analytical data is achieved by enrichment of the air sample before trapping, with a stable isotope permeation tube system. The same principles have been applied to a new instrument, specifically designed for operation on an electric vehicle (Ducato Elettra, Fiat). The zero emission vehicle and the fully transportable, battery-operated GC/MS system provide a unique possibility of monitoring benzene exposure in real everyday situations such as while driving, refuelling, or repairing a car. All power consumptions have been reduced so as to achieve a battery-operated GC/MS system. Liquid nitrogen cryofocusing has been replaced by a packed, inductively heated, graphitized charcoal microtrap. The instrument has been mounted on shock absorbers and installed in the van. The whole system has been tested in both fixed and mobile conditions. The maximum monitoring period without external power supply is 6 h. The full analytical cycle is 4 min, allowing close to real-time monitoring, and the minimum detectable level is 1 μg/m3 for benzene. In-vehicle monitoring showed that, when recirculation was off and ventilation on, i.e., air from outside the vehicle was blown inside, concentrations varied widely in different driving conditions: moving from a parking lot into normal traffic on an urban traffic condition roadway yielded an increase in benzene concentration from 17 to 62.3 μg/m3 even if the actual distance was small. A larger increase was observed when a car was left with the engine running at a distance 2 m from the zero emission vehicle: We measured an increment of benzene concentrations from 15.2 to 174.4 μg/m3 with a car equipped with a catalytic converter, and from 19.1 to 386.3 μg/m3 with a car without such a converter.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Estuarine waters ; Solid-phase extraction ; Triazines, alachlor, metolachlor ; Nitrogen phosphorus detection
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The stability of atrazine, simazine, alachlor, metolachlor, and deethylatrazine on C18 Empore disks has been determined. Estuarine water (100 mL) spiked at 3 μg L−1 with the target pesticide mixture was preconcentrated on the disks; the disks were then stored at −20°C, 4°C, and at room temperature for periods up to three months and were analyzed by gas chromatography with nitrogen-phosphorus detection. Complete recovery was observed after storage at −20°C throughout the period of the study. Losses up to maximum of 10% were observed after storage at 4°C. Higher losses (up to 24% for alachlor) occurred only at room temperature; the coefficient of variation for these determinations (8–11%) was also higher than that for the others (3–5%). The stability of the pesticides was dependent on the water matrix, on storage temperature, and on properties such as vapor pressure and water solubility.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Chromatographia 42 (1996), S. 660-664 
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Unified retention data ; Alkanes, alkenes, naphthenes and aromatics ; Squalane
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Gas chromatographic, unified retention data of 120 hydrocarbons including: alkanes, alkenes, alkynes, alkylcycloalkanes, alkylcycloalkenes, aromatics and dienes on squalane stacionary phases are given. These values agree well with the corresponding experimental values used in the statistical treatment of the experimental data.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Dialkylhydrazones ; Kováts retention indices ; Structure-retention relationships
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary N,N-Dialkylhydrazones [DAHs; R1R2C=1N-2N(R3)2] were prepared and their Kováts retention indices determined on 100% dimethylpolysiloxane (HP-1) and 5% diphenyl and 95% dimethylpolysiloxane (HP-5) stationary phases. The physico-chemical and retention behaviour of the DAHs depend greatly on whether R2=H or an alkyl group. A similar difference is observed in the alkane and oxo homomorphic factors of DAHs formed from aldehydes or ketones. The difference is explained on the basis of NMR and quantum-chemical results by intramolecular interactions between R2 and the lone pair of the2N atom. A single linear equation is suitable for prediction of retention indices if parameters are introduced representing resonance structure (bond angle and electron density) besidesI oxo or the van der Waals' surface.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Chromatographia 42 (1996), S. 462-464 
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Alcohols ; Cellulose tribenzoate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Cellulose tribenzoate (CTB) has some desirable operational properties and special interactions with alcohols. When chromatographic separation is carried out at 150°C, the C1–C4 alcohols have enhanced retention and other alcohols are eluted rapidly. Some probe molecules were used to characterize the chromatographic behavior of CTB by calculating the adsorption enthalpy (−ΔHa) between the sample and stationary phase. Separation of aliphatic alcohols was successfully performed on a packed column with a support (GDX) coated with CTB and temperature programming improved the separation of these alcohols.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Reversed-flow technique ; Rate constants ; Bimolecular gaseous reactions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Rate constants for bimolecular reactions in the gas phase, under diffusion controlled conditions, can easily be determined by the reversed-flow gas chromatography (RF-GC) technique. The analysis of the diffusion band by means of a simple PC programme gives directly an apparent, second-order rate constant for gaseous reactions. By varying the amounts of the reactants, one can calculate the true order of the reaction and the true non-first-order rate constant of gaseous reactions. The calibration problem of the analytical techniques in non-first-order reaction kinetics is absent as are other disadvantages connected with carrier gas flow, peak shape and their instrumental spreading. The method can be used for atmospheric reactions and was applied in the gaseous reaction systems: SO2+NO2, SO2+Br2, C6H6+NO2, C6H5CH3+NO2 and C3H6+NO2 with various concentrations of reactants in nitrogen. The effect of the NO2 concentration on the apparent second-order rate constant of C2H4+NO2 at 333.2 K was also studied. Finally, the effect of sun light pre-irradiation of C2H2+NO2 in nitrogen was investigated.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Molecular absorption spectrometry ; Gas phase detection ; Benzene derivatives
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A simple and inexpensive detection system for gas chromatography, based on gas-phase, molecular absorption measurements, is presented in which the chromatographic column is directly joined to the spectrophotometer flow cell, without heated transfer lines. A mixture of eight benzene compounds (including methyl, halogen and nitrogen derivatives) were separated and analyzed. Parameters affecting separation (temperature program and carrier gas flow) and measurement quality (wavelength and integration time) were studied and a measurement program designed to modify the wavelength during chromatography. The analytical characteristics of each compound were calculated, obtaining detection limits ranging from 0.5 to 9 μg mL−1. Finally, the method was applied to several synthetic mixtures, with good results.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Chromatographia 42 (1996), S. 465-468 
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Packed column separations ; Pyridine and alkylpyridines
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The gas chromatography of the β-picolines in a lowboiling tar base fraction, is described. The methods developed employ packed columns with binary phases containing N,N,N′,N′-tetrakis(2-hydroxypropyl) ethylenediamine plus metal transition stearate, or with a ternary phase containing this mixture and o-hydroxyethylresorcinol
    Type of Medium: Electronic Resource
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  • 11
    Electronic Resource
    Electronic Resource
    Springer
    Chromatographia 42 (1996), S. 547-550 
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Supercritical Fluid Extraction ; Pesticides Residues ; Chlorothalonil ; Appels
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A new method for the extraction of Chlorothalonil residues from apples using supercritical CO2 as the extracting fluid is described. The supercritical fluid extraction results were compared with those obtained by solid-liquid extraction. The results showed that SFE is faster and more selective with better recovery and higher selectivity.
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  • 12
    Electronic Resource
    Electronic Resource
    Springer
    Chromatographia 42 (1996), S. 578-582 
    ISSN: 1612-1112
    Keywords: Gas chromatography ; EDTA determination ; DTPA determination ; Water analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A new analytical method and the method validation for the determination of ethylenediaminetetraacetic acid (EDTA) and diethylenetriaminepentaacetic acid (DTPA) in lake and sea water is presented. An aqueous sample, after evaporation to dryness, was treated with an esterification reagent. The resulting ethyl ester derivates were determined by capillary gas chromatography using a nitrogen phosphorus specific detector (GC-NPD). The response was linear up to 5 mg L−1. The recoveries from lake and sea waters were 59–105 % for EDTA and 86–112 % for DTPA. The run-to-run repeatabilities (R.S.D.) were 2–8 % for EDTA and 4–11 % for DTPA depending on concentration and the reproducibilities (R.S.D.) were 6–13 % and 3–11 %, respectively. The limits of detection for EDTA and DTPA were 3 and 12 μg L−1 in distilled water, respectively. The method is simple to use and reliable as shown by the analysis of samples of lake water that is influenced by pulp and paper industry.
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  • 13
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Electron capture detection ; Mass spectrometric detection ; Atomic emission detection ; PCBs in marine sediments
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Electron capture detection (ECD), low- and highresolution mass spectrometry (LR- and HRMS), and atomic emission detection (AED) were compared for the gas chromatographic (GC) detection of polychlorinated biphenyls (PCBs) present in highly contaminated marine sediments. With ECD, LRMS, and even HRMS, detection was seriously disturbed by the complex matrix of the sediments, whereas AED in the chlorine-selective mode provided excellent PCB profiles without interferences. In addition, GC-AED provided congener independent responses, which enabled accurate quantitation of all PCBs based on a single calibration curve. However, because GC-AED was less sensitive than the other techniques studied, preparation of relatively large amounts of sample (10–20 g dry sediment) was required for most analyses.
    Type of Medium: Electronic Resource
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  • 14
    Electronic Resource
    Electronic Resource
    Springer
    Chromatographia 43 (1996), S. 73-75 
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Spatial average gas velocity ; Temporal average gas velocity ; Column pressure drop
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary While the commonly known temporal average velocity of a carrier gas is approximately proportional to the pressure drop along a column, the spatial average velocity is exactly proportional to that pressure.
    Type of Medium: Electronic Resource
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  • 15
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Electron capture detection ; Solid phase extraction ; Chlorophenols ; Water analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A solid-phase extraction system coupled to a gas chromatograph fitted with an electron capture detector was developed for the determination of chlorophenols in waters. The continuous system consists of an XAD-2 adsorbent column where chlorinated phenols are preconcentrated and subsequently eluted with ethyl acetate. The sensitivity of the method is proportional to the number of chlorine substituents in the phenol; thus, the detection limit for monochlorophenols is ca. 10 μg L−1 and that for pentachlorophenol about 2 ng L−1. The method was used to determine chlorophenols in treated waters, with good precision; however, no mono or dichlorophenols were detected at the levels afforded by the proposed method.
    Type of Medium: Electronic Resource
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  • 16
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Retention indices ; Correlation equations ; n-Alkylcyclopentenes andn-alkylcyclohexenes ; n-Alkyl esters
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Correlation equations have been derived which relate the Kováts retention indices ofn-alkylcyclopentenes,n-alkylcyclohexenes andn-alkyl esters of aliphatic acids on the stationary phases OV-101, OV-225 and PEG 20M to column temperature and carbon number in the alkyl chain. The universal equation: $$\begin{gathered} RI = A + B \cdot m + C \cdot \log (m)/m + \hfill \\ D/[(m - 2)^2 + 0.1] + Et \hfill \\ \end{gathered} $$ whereA, B, C, D andE are correlation coefficients,m is the number of carbon atoms in the side chain (forn-alkylcycloalkenes) or in the alcohol chain (for alkyl esters) andt is the column temperature, describes the retention indicesRI of these homologous series with high accuracy (SD〈1 index unit), beginning with the first members of the series.
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  • 17
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Solid phase extraction ; Nitrogen phosphorus detector ; SCH 44643 in rat plasma
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A gas chromatographic (GC) assay for the determination of SCH 44643, an orally active antagonist of responses to both histamine and PAF, was developed and validated for rat plasma. The method involved organic solvent extraction followed by solid phase extraction on aminopropyl column. The separation was on a capillary column (DB-17) with quantitation by a nitrogen-phosphorus detection. The method was sensitive with a limit of quantitation of 5 ng mL−1. There was a good linear relationship between the peak height ratio (SCH 44643/internal standard) and SCH 44643 concentration in the range 5 to 200 ng mL−1. The method was precise with a coefficient of variation ranging from 1.8 to 3.0% and accurate with a bias ranging from 0 to 5.8%. Moreover, SCH 44643 was stable in rat plasma after being subjected to three freeze-thaw cycles. The assay was shown to be sensitive, specific, accurate and precise, and suitable for use in pharmacokinetic or toxicokinetic studies.
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  • 18
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Poly(L-glutamate) ; Cholesteric liquid crystal ; Properties as stationary phases
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Comparative gas chromatographic properties of two thermotropic Poly(L-glutamates) with long alkyl side chains (10 and 16 carbons called Poly 10 and Poly 16 respectively) are studied. Their thermal properties were established with differential scanning calorimetry (DSC) and gas chromatography. They present a cholesteric liquid crystal in a large temperature range. The chromatographic separation abilities of the two polymers in the liquid crystal state were studied using capillary glass columns. Interesting analytical performances were obtained in different fields: isomeric separation of alkanes, aromatics, polyaromatics, volatile aroma compounds and cis and trans isomers. Some differences were noticed in their behaviours; 2 and 3-methyloctane and xylene isomers are separated only on Poly 10 while limonene and eucalyptol are separated only on Poly 16.
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  • 19
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Aliphatic hydrocarbons ; Chlorinated aromatics ; Pork liver extracts
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A multicomponent extraction/concentration procedure has been developed for the enrichment of PCBs, PCTs and aliphatic hydrocarbons (pristane, C18, C19, C20, C22, C24, C28, C32 and C36) in pork liver. These components of the enriched extract were then simultaneously determined by gas chromatography. Mean recoveries ranged from 81.5% for pristane to 93% for PCBs;CV% (0.9–6.7) indicated the method to be both precise and reproducible.
    Type of Medium: Electronic Resource
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  • 20
    Electronic Resource
    Electronic Resource
    Springer
    Chromatographia 42 (1996), S. 77-82 
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Modified alumina ; Coal mine air ; Alkenes, alkanes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A gas chromatographic method for the separation of alkanes and alkenes present in coal mine air has been developed using modified alumina columns. The separation was carried out using a GC equipped with a gas sampling valve, a FID and a surface modified alumina packed column with helium as carrier gas. An investigation was carried out into the effects of surface modifiers on alumina. The study examined the change in retention properties on alumina modified by alkali metal salts and the specific effects of the halide anions and metal cations. The paper describes the preparation of the alumina columns and the effects on selectivity of post heating the stationary phase. The study demonstrated that alumina modified with 2% sodium chloride and post heated to 150°C was the most appropriate stationary phase.
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  • 21
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Headspace sampling ; Solid-phase microextraction (SPME) ; Nitrogen-phosphorus detection (NPD) ; Organophosphate pesticides
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Organosphosphate pesticides have been found extractable by headspace solid-phase microextraction (SPME), and the best conditions of their extraction from human whole blood and urine samples have been investigated. The body fluid samples containing nine pesticides (IBP, methyl parathion, fenitrothion, malathion, fenthion, isoxathion, ethion, EPN and phosalone) were heated at 100°C in a septum-capped vial in the presence of various combinations of acid and salts, and SPME fiber was exposed to the headspace of the vial to allow adsorption of the pesticides before capillary gas chromatography (GC) with nitrogen-phosphorus detection. The heating with distilled water/HCl/(NH4)2SO4/NaCl and with distilled water/HCl gave the best results for urine and whole blood, respectively. Recoveries of the nine pesticides were 0.8–10.6% except for phosalone (0.03%) for whole blood, and 3.8–40.2% for urine. The calibration curves for the pesticides showed linearity in the range of 50–400 ng/0.5 mL for whole blood except for malathion (100–400 ng/0.5 mL whole blood) and 7.5–120 ng/0.5 mL for urine except for phosalone (15–120 ng/0.5 mL urine) with detection limits of 2.2–40 ng/0.5 mL for whole blood and 0.8–12 ng/0.5 mL for urine.
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  • 22
    Electronic Resource
    Electronic Resource
    Springer
    Chromatographia 42 (1996), S. 309-312 
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Graphite coated capillary columns ; Ephedrines separation ; Drug analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The preparation of graphite-layer capillary column is described together with their application to the analysis of aliphatic and aromatic amines. Attention is mainly focused on the separation of ephedrines which, being sympathomimetic amines, are often present in pharmaceutical preparations, but are also illegally used by athletes as stimulants. Complete separation of these compounds, using direct GC-NPD analysis of human urine extract, without derivatisation, has been obtained.
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  • 23
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Column liquid chromatography ; Pesticide residues ; Surface water analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A monitoring programme based on gas chromatography (NPD, ECD) using MSD for confirmatory purposes and coupled-column liquid chromatography was applied to the analysis of pesticide residues in surface water from a predominantly agricultural area of Spain (Comunidad Valenciana). Samples analysed by means of enzyme-linked immunosorbent assay gave similar results to those obtained by GC (MSD) for the determination of total triazines. The test employed had the advantages of a simple test procedure, short analysis time and high confirmatory value. Nevertheless, the multiresidue character, accuracy and unequivocal identification of individual pesticide residues of GC (MSD) make this technique the most appropriate for environmental monitoring programmes. In this monitoring programme about 200 samples were analysed between 1993–1994. 27 different pesticides were detected in 91 of these samples. The pesticides more frequently detected were dimethoate, methidathion, endosulfan A and B, endosulfan sulphate and pirimicarb. The highest concentrations found were 39.9 μg L−1 of dimethoate, 10.6 of pirimicarb and 10.6 of methidathion.
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  • 24
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Supercritical fluid extraction ; Pesticide residues ; Norflurazon residues ; Oxadixyl residues ; Food crops
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Norflurazon and Oxadixyl residues have been analysed by HRGC-ECD after extraction from field-treated sugar cane and grapes using classical solid-liquid extraction or supercritical fluid extraction. The extraction techniques were compared; the results indicate the advantages of SFE as an alternative method for analysis of pesticides in these samples.
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  • 25
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Microwave extraction ; Sample clean-up ; Organochlorine compounds ; Blubber of marine mammals
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A rapid and effective method is described for the extraction of organochlorine compounds (PCB 153, PCB 138, PCB 180, p,p′-DDE, α-HCH, γ-HCH, ε-HCH and HCB) from seal blubber and pork fat withn-hexane using a microwave technique. Heating of the non-polarn-hexane was achieved using a microwave transformer. The lipid content of the samples obtained by this extraction was identical to that by Soxhlet extraction. After separation of sample matrix and organochlorines on a silica gel column the organochlorine compounds were determined by GC-ECD. The efficiency of the method was tested with 500 mg spiked fat, extracted using various numbers of extraction cycles. Recoveries of organochlorine compounds in grey seal blubber and spiked pork fat generally exceeded 90 %.
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  • 26
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Solid phase micro extraction ; Chloroethenes ; Reductive dechlorination
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary An analytical method has been developed to determine the chloroethene series, tetrachloroethene (PCE), trichloroethene (TCE),cisdichloroethene (cis-DCE) andtransdichloroethene (trans-DCE) in environmental biotreatment studies using gas chromatography coupled with a solid phase micro extraction (SPME) technique. The volatile chlorinated compounds in aqueous solution can be analyzed directly without solvent extraction, purge and trap, or thermal heating. The calibration curves have demonstrated good linear relationships within 50.0 to 3000.0 μg L−1 concentration range. Detection limits are 18.0, 5.0, 25.0, and 42.0 μg L−1, for PCE, TCE,cis-DCE andtrans-DCE, respectively. Factors which affect the SPME process, such as sample adsorption time, thermal desorption time, and concentration of salt in the matrix, have also been evaluated.
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  • 27
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Local anaesthetics ; Solid phase micro extraction (SPME) ; Direct immersion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Local anaesthetics have been shown to be extractable from human whole blood samples by direct immersion (DI)-solid phase micro extraction (SPME). After deproteinization with perchloric acid, the pH of the clear supernatants of human whole blood samples containing the drugs were adjusted to about 7 with 10 M NaOH in the presence of NaCl; a polydimethylsiloxanecoated SPME fiber was then immersed directly into the sample solution to allow adsorption of the drugs before capillary gas chromatography (GC) with flame ionization detection. The DI-SPME for 1-mL whole blood gave peaks for all the drugs; only a small amount of background noise appeared and this gave no problems in the detection of the drugs. Recoveries of the ten drugs from human whole blood was 0.74–19.7 %. The calibration curves for seven drugs showed linearity in the range of 0.25–12 μg mL−1 whole blood, with detection limits of 54–158 ng mL−1.
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  • 28
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Stationary phase ; β-Cyclodextrin ; Separation mechanism
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Three peralkylated β-cyclodextrins (CD), perethylated β-CD, perbutylated β-CD and peroctylated β-CD have been coated on to untreated fused-silica capillary tubing and used to separate some achiral and chiral compounds. The separation mechanism is discussed in the paper.
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  • 29
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Dicofol ; Fish ; Lethal concentration ; Bioconcentration factor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Evaluation of the toxicity of Dicofol was carried out onAstyanax bimaculatus schubarti, a characteristic fish species living in tropical rivers and lakes. Experiments were under laboratory controlled conditions with atmospheric air flow and dilution water at 25°C in the static mode. Fish samples were collected and submitted to appropriate analytical procedure: Soxhlet extraction, clean-up by Florisil adsorbent and finally quantification by GC-ECD. The results showed good recoveries (〉 89%) for the developed method both in water and fish samples. The lethal concentration, LC50, and the bioconcentration factor, BCF, were 18.13 mg L−1 and 241.70, respectively forAstyanax bimaculatus schubarti demonstrating the lipophilic nature of the studied compound.
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  • 30
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Electronic pressure control ; Mass selective detector ; Pesticide residues ; Cereals
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary An analytical method for the confirmation of 30 pesticide residues in cereals and related products has been developed. Splitless injection with electronic pressure control using constant carrier gas flow gives higher sensitivity and better resolution than electronic pressure control and isobaric analysis. The use of electronic pressure control assures consistent retention times enabling selected ions to be collected in short time windows. Mass spectrometric detection in the selected ion monitoring mode using three ions for each pesticide ensured good sensitivity and accurate pesticide confirmation.
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  • 31
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    Chromatographia 43 (1996), S. 208-210 
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Epoxystyrenes ; Retention index
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The separation of some epoxystyrenes on fused silica capillary columns coated with poly(ethylene glycol) was investigated, Retention indices were determined at two temperatures to interpret chromatographic behaviour, The standard deviation was 0.3 index units.
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  • 32
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Microwave-assistend solvent extraction (MASE) ; Pesticide residue analysis ; Triazine herbicides ; Soil samples
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The use of microwave-assisted solvent extraction (MASE) as an alternative for conventional solvent extraction procedures for the determination of some triazine herbicides in soil samples has been investigated. In this study MASE method development was focused on the selection of a suitable extraction solvent prior to the instrumental analysis of uncleaned extracts with gas chromatography and nitrogen-specific detection. A mixture of dichloromethane-methanol (90∶10, v/v) yielded recoveries ranging from 89 to 103 (spiked level 200 μg/kg) with RSDs ranging from 2.1 to 5.3%. This solvent mixture is also very convenient for further procedure. The selected MASE procedure was tested by analyzing freshly spiked soil samples and samples with aged residues of atrazine, desethylatrazine, desisopropylatrazine and simazine. The results were compared with those obtained by a conventional liquid extraction method. The comparative study indicated that MASE yields recoveries at least as good as those obtained by the conventional method. Moreover, the MASE procedure provides low solvent consumption in combination with a high sample throughput.
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  • 33
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Fosfomycin in urine ; Pharmacokinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A capillary gas chromatographic method for the determination of fosfomycin in human urine is described. After dilution of the sample and derivatization, analysis was on a HP-1 capillary column and a flame ionization detector was used to determine the bistrimethylsilyl derivative of fosfomycin. Response was linear in the range 50–5000 μg mL−1. The detection limit was about 10 μg mL−1. The within and between day coefficients of variation did not exceed 6%. The method was applied to the determination of fosfomycin in urine samples collected during clinical pharmacokinetic studies.
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  • 34
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Sulfur chemiluminescence detector ; Flame ionisation ; Dual-channel detection ; Optimization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The dual-channel detection of samples with detectors coupled in series is possible only when the first detector is a non-destructive one. However, the configuration where a destructive detector, such as the flame ionization detector (FID), is followed by the flameless, sulfur chemiluminescence detector (flameless SCD) can be used to detect simultaneously carbon and sulfur. In this work, the FID and flameless SCD are coupled in series for dual-channel detection of sulfur compounds in three gasoline samples. Optimum conditions for flameless SCD were evaluated by altering the flow rates of hydrogen and air and the oxygen pressure to the ozone generator. Samples are identified by retention indices where the homologous n-alkylthiols are used as standards. The increment in retention index per carbon number of the n-alkylthiols is 105.54 in the Quadrex 007 series, 0.32 mm i.d., 4 μm film, column.
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  • 35
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Stationary phase ; Polysiloxane matrices ; β-Cyclodextrin ; Crown ether ; Liquid crystal ; Coordination effect
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary This paper investigates the possibility of using a sidechain crown ether polysiloxane (PDB-14-C4) and a side-chain liquid-crystalline polysiloxane-containing crown ether (PSC-3) as matrices for peralkylated β-CD employed as stationary phases. Three columns, coated with PSC-3 + permethylated β-CD, PDB-14-C4 + permethylated β-CD and PDB-14-C4 + perethylated β-CD were characterized by gas chromatography. The column efficiencies, phase transitions, and selectivities were measured and compared.
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  • 36
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    Chromatographia 42 (1996), S. 63-71 
    ISSN: 1612-1112
    Keywords: Gas chromatography ; High efficiency open tubular columns ; Columns connected in series ; Gasoline analysis ; Detailed hydrocarbon analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary More than 1.3 million effective plates were produced by a column 450 meters long, 200 μm inner diameter. The column was built up by connecting nine 50 meter columns in series. The sum of the efficiencies of the individual pieces equalled the efficiency of the combined column. Up to 970 components were differentiated in a gasoline standard.
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  • 37
    ISSN: 1612-1112
    Keywords: Gas chromatography ; flame photometric detector ; Sulfur in diesel fuel
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A new method is proposed for the computerized determination of sulfur in diesel fuel by capillary gas chromatography with a flame photometric detector (FPD). The diesel fuel is injected in the gas chromatograph after dilution with n-hexane. After recording the chromatogram, the sulfur content in the diesel fuel (mg L−1 or w/w) is given directly by an integrator provided with a Basic card or by a personal computer in which the algorithm of the calibration curve has been entered. Use of a calibration curve does not require the identification of the numerous sulfur compounds present in diesel fuel. The calibration curve was corrected for the quenching effect that the hydrocarbon components of the diesel fuel produce on the detector response. The method was tested using diesel fuel with a known sulfur concentration and was found to be very accurate; it is reproducible, fast and may be automated.
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  • 38
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Semivolatile flavor compounds ; Cinnamon ; Solid-phase microextraction ; Chemometric classification
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The conditions which affect the reproducibility of characteristic chromatographic profiles of semivolatile compounds from true cinnamon and cassia by headspace solid-phase microextraction are determined. Optimum conditions for sample amount, vial size, temperature, sampling time, and fiber type for steady state sampling conditions are identified. Vial size was an unexpected critical parameter possibly related to the build up of internal ternal pressure during sample heating followed by expulsion of a portion of the vapor phase through the septum as it was punctured by the syringe. Gas chromatography with ion trap mass spectrometry was used to identify the major volatile compounds in cassia and true cinnamon. Reasonable semi-quantitative agreement (r 2〉0.87 and generally greater than 0.93) was observed for the major semivolatile compounds isolated by headspace solid-phase microextraction and solvent-assisted supercritical fluid extraction. The extracts isolated by solid-phase microextraction contained relatively high concentrations of terpene-type compounds in low abundance in the solvent-assisted supercritical fluid extracts, but these compounds were of little value in distinguishing the botanical origin of authentic cinnamon and cassia samples. The latter were easily distinguished by the presence of eugenol and benzyl benzoate in true cinnamon, that was absent in cassia, and the presence of coumarin and δ-cadinene, in cassia, that was either absent or in low concentration in true cinnamon. Headspace solid-phase microextraction provides a rapid and simple method for establishing the botanical origin of the principal cinnamons of commerce.
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  • 39
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Atomic emission, electron capture ; and nitrogen phosphorus detection ; Honey ; Acaricides
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The performance of a gas chromatographic system coupled to an atomic emission detector (GC/AED) is tested by comparison with a two-dimensional gas chromatographic system equipped with capillary columns of different polarity and simultaneous electron capture and nitrogen-phosphorus detection (ECD/NPD), for the determination of the acaricides chlordimeform, bromopropylate, amitraz and coumaphos on spiked honey samples. The acaricides were extracted with ann-hexane/acetone mixture (80∶20, v/v) with a further clean-up step on an octadecylsilane cartridge. The 193 nm carbon emission line is the best choice in terms of sensitivity whereas the ECD/NPD system gives better selectivity.
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  • 40
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Low-molecular-weight hydrocarbons ; Extraterrestrial atmospheres ; Chemically bonded squalene(ane) phase ; 13C and29Si CP-MAS NMR
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Chemically bonded squalene(ene) phases have been synthesized via a hydride modified silanization process using dimethylchlorosilane, triethoxysilane and trichlorosilane. The surface structure of the bonded phases were characterized with DRIFT and solid state NMR studies. The results of the latter indicate successful bonding of a non-terminal olefin to the silica surface and that bonding of individual squalene molecules appeared not to occur at the same site(s) presumably due to steric hindrance. Among the phases examined, the trichlorosilane-based material exhibits better chromatographic properties probably due to greater surface coverage and hence effective non-polar interaction between the solutes and the bonded ligands. Under isothermal conditions, the present packings produced fast and efficient separation of C1–C4 saturated hydrocarbons on shorter columns than similar columns containing alkyl- or bidentate alkyl-modified silica packings at low column head pressure and are thermally stable at temperatures up to 250°C or higher.
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  • 41
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    Chromatographia 42 (1996), S. 431-434 
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Fatty acid methyl esters ; Biodiesel ; Methanol ; Glycerol
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The methanol and free glycerol content of vegetable oil methyl esters used as diesel fuel (biodiesel) is very important in describing the quality of this fuel and is therefore limited by specifications. A previously described GLC method for the determination of free glycerol in biodiesel has been further developed and also allows the simultaneous determination of methanol. Sample preparation includes dissolving in dimethylformamide, silylation with bis-trimethylsilyltrifluoracetamide (BSTFA) and separation on a methylsilicone fluid, coated-capillary column using either FID or MS-detection. Ethanol and 1,4-butanediol were used as internal standards. Both detection systems show sufficient sensitivity for concentrations relevant to biodiesel samples. The recovery was tested using a RME-sample containing known amounts of methanol and glycerol.
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  • 42
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Bonded silicas ; Phase transitions ; Differential scanning calorimetry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary In order to give a molecular interpretation to the phase transition observed with densely bonded octadecyl-silicas in reversed phase liquid chromatography (RPLC) as well as in gas chromatography (GC), nine new bonded silicas were prepared including grafts with polar groups at the extremities of long spacers (18 carbon atoms). The interpretation is simplified by using large-pore macroporous substrates and inverse GC in conjunction with differential scanning calorimetry (DSC) as the test method. A phase transition is observed in almost all cases, but the temperature range is lower and more extended in comparison to the dimethyloctadecyl reference silica. An interpretation of the phase transition is given, based on the folding of the chains and the resulting “autodensification” of the layer.
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  • 43
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    Chromatographia 42 (1996), S. 593-594 
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Double-base propellants ; Nitroglycerin ; Centralite I ; Dibutyl phthalate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The separation and quantitative determination of propellant constituents on short, wide-bore fused-silica capillary columns, coated with crosslinked methylsilicone phase was investigated. The analytical results were quite satisfactory.
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  • 44
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Partition coefficients ; Henry's constants ; High density polyethylene ; Polymer drying
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Gas-solid partition coefficients (K) for n-hexane in high density polyethylene (HDPE) have been measured at conditions applicable to large-scale drying utilizing a novel headspace method. The method features considerable versability and simplicity due to the control of experimental conditions designed to favor full extraction of the analyte into the headspace. By combining this full extraction technique with a traditional static headspace experimental scheme, a method which measuresK and residual concentration is achieved. The results show that partition coefficients differ significantly between HDPE in its virgin powder and pellet forms, as well as among various HDPE grades. The differences are shown to be attributable to differences in % crystallinity of the specific polymer. Data collected over a wide range of hexane concentrations reveals saturation levels (solubilities) which correspond to crossover from evaporative to diffusion-controlled drying.
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  • 45
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    Chromatographia 43 (1996), S. 625-627 
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Headspace sampling ; Formaldehyde ; Plastics ; Foods ; Biological samples
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A modified headspace gas chromatographic method, based on polycondensation with formaldehyde, has been developed for derivatization with formaldehyde in foods, biological media and other products. The method provides the possibility of obtaining results within three minutes, which is of significant importance for the control of food and cosmetics production and the quality of polymer products based on formaldehyde, as well as for biological monitoring.
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  • 46
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    Chromatographia 43 (1996), S. 159-162 
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Gas pressures ; Gas compressibility ; Retention volumes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The true meanings of the so-called corrected retention volume and the specific retention volume are explained in the light of the recent paper by Davankov.
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  • 47
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    Chromatographia 43 (1996), S. 163-176 
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Retention index estimation ; Aromatic compounds ; Incremental models
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Pure topologically based incremental models have been developed in order to estimate the retention indexes of aromatic compounds substituted with groups containing the hetero atoms nitrogen, oxygen and halogens. The bond-types of the compounds are counted and used as molecular descriptors. The observed estimation errors are about 1 % for compounds containing no hetero atoms and for those containing halogenated substituents; the errors are approximately 2 % for aromatic compounds with nitrogen- and oxygen-containing substituents. The method is validated by prediction of the retention indexes for an additional group of aromatic compounds (the validation data set).
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  • 48
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Molecular modelling ; Molecular mechanics calculations ; Permethylated α-, β- and γ-cyclodextrins ; Interaction mechanism
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The capillary gas chromatographic retention behavior of α-pinene and tricyclene has been investigated on stationary phases of different polarities. On all but one of the columns employed, tricyclene eluted before α-pinene; only permethylated β-cyclodextrins dissolved in moderately polar polisiloxanes gave a reversed elution order. The intermolecular interactions which caused the unexpected retention behavior were investigated in detail, applying methods of computer simulation. To achieve this, we have developed a calculation algorithm on the basis of molecular mechanical optimizations and programmed it in a macro. This makes it possible to systematically investigate a given configuration space in which all the possible interactions can take place. It was shown that permethylated β-cyclodextrin as host molecule for both guest molecules offers an optimum cavity size. As a result the number of energetically favorable contacts between host and guest molecules as well as the strength of the interactions in this stationary phase were larger. As a consequence the elution order, normally only influenced by the vapor pressure of the compounds at a given temperature, was changed. Nonspecific interactions played an especially important role for these kinds of substances.
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  • 49
    ISSN: 1612-1112
    Keywords: Column liquid chromatography-gas chromatography ; Gas chromatography ; 3,5-Stigmastadiene ; Cold pressed olive oil
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The quantitation of 3,5-stigmastadiene and other steroidal hydrocarbons, commonly known as steradienes, is a valid tool for the recognition of refining (in particular bleaching) of edible oils; the evidence of this process is nowadays of a great interest due to growing market for “virgin”, cold-pressed, “natural” oils. Due to the long time required (about 4 hours) and the amount of solvents employed (about 650 mL) to perform the official analysis, other methods have been recently proposed, the most important of which involves high performance liquid chromatography coupled with capillary gas chromatography (HPLC-GC). In this study the results of ten oil samples, analysed by both the official method and HPLC-GC, are reported and the two methods compared and discussed, for routine use, in terms of sample preparation, time of analysis and setting up, difficulty and reproducibility.
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  • 50
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Zeolite membrane PLOT columns ; In-situ synthesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The preparation of a zeolite membrane PLOT column by in-situ synthesis is described. The advantages of this new column are discussed. Some analytical applications to alkanes, arenes, esters, alkyl halides and ethers on the zeolite membrane PLOT column compared with those on a coated zeolite PLOT column are reported.
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  • 51
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Column liquid chromatography ; ECD, UV and MS detection ; EPA Method 515.1 ; Chlorinated acidic pesticides
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A comparison of the official EPA method 515.1 for determination of chlorinated acidic pesticides and a modification of it is illustrated. Extraction of the analytes from water and their determination and quantitation is by gas chromatography-electron capture detection (GC-ECD), liquid chromatography-UV detection and liquid chromatography-particle beam mass spectrometry. Although HPLC-PBMS was found to be less sensitive than the GC-ECD method, it was, nevertheless, more sensitive than HPLC-UV. The modified method is simpler, quicker and allows more accurate determination of pesticides in aqueous samples.
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  • 52
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    Chromatographia 43 (1996), S. 296-300 
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Thermal desorption ; Ion-pair column liquid chromatography ; Nicotine, 3-ethenylpyridine ; Environmental tobacco smoke
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Different sampling and analysis techniques for the determination of gas-phase nicotine and 3-ethenylpyridine in environmental tobacco smoke are reported. Graphitized carbon traps, annular diffusion denuders, and nebulizer collectors have been used as sampling devices in combination with either thermal desorption or with water extraction. Capillary gas chromatography and ion-pair reversed-phase chromatography were applied to desorbed and liquid samples obtained in an intercomparison indoor study. The methods developed here show some advantages over existing methods in terms of analysis time, sensitivity and loading capacity.
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  • 53
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Electron-capture detector ; Photoionization detector ; Pulsed discharge detector
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Since the electron-capture detector (ECD) is highly selective, it is imperative to use a more universal ionization detector in conjunction with the ECD in order to detect non-capturing or weakly capturing compounds. Also in an EC study of weakly or moderately strong electron-capturing compounds, it is necessary to identify the EC peak of the compound by identifying the major component with an ionization detector. In this paper we have shown that the pulsed discharge detector can be interchanged between the EC and the helium ionization modes within 4–6 s. The application of this procedure has been illustrated with a mixture of alkane/alkene chlorocompounds. The interchange between EC and argon photoionization modes has also been investigated. The change from EC to argon photoionization also occurs in 4–6 s but the reverse process requires ∼9 s.
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  • 54
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Solid-phase micro extraction (SPME) ; Headspace sampling ; Ethanol ; Alcohol
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Ethanol has been found extractable from human whole blood and urine samples by headspace solid-phase micro extraction (SPME) with a Carbowax/divinylbenzene-coated fiber. After heating a vial containing the body fluid sample with ethanol, and isobutanol as internal standard (IS) at 70°C in the presence of (NH4)2SO4, a Carbowax/divinylbenzene-coated SPME fiber was exposed in the headspace of the vial to allow adsorption of the compounds. The fiber needle was then injected into a middle-bore capillary gas chromatography (GC) port. The headspace SPME-GC gave intense peaks for both compounds; a small amount of background noises appeared, but did not interfere with the detection of the compounds. Recoveries of ethanol and IS were 0.049 and 0.026% for whole blood, respectively, and 0.054 and 0.085% for urine, respectively. The calibration curves for ethanol showed excellent linearity in the range of 80–5000 mg L−1 for whole blood and 40–5000 mg L−1 for urine; the detection limits for both samples were 20 and 10 mg L−1, respectively. The data on actual determination of ethanol after the drinking of beer are also presented for two subjects.
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  • 55
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    Chromatographia 43 (1996), S. 444-446 
    ISSN: 1612-1112
    Keywords: Gas chromatography ; History of chromatography
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary In November 1995, theDeutsches Museum, the world's largest technical museum, opened a new branch in Bonn, devoted to achievements after 1945. There, the first gas chromatographic system used by Erika Cremer and Fritz Prior, in 1945–47, in Innsbruck, is exhibited. The new display is described and the early activities of Erika Cremer and her students are summarized.
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  • 56
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Solid-phase microextraction ; Headspace sampling ; Phencyclidine (PCP) ; Surface ionization detection (SID)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Phencyclidine (PCP) was found to be extractable by headspace solid-phase microextraction (SPME) from human whole blood and urine. Sample solutions were heated at 90°C in the presence of NaOH and K2CO3, and an SPME fiber was exposed in the headspace of a vial for 30 min. Immediately after withdrawal of the fiber, it was analyzed by gas chromatography with surface ionization detection (GC-SID). Recoveries of PCP were approximately 9.3–10.8% and 39.8–47.8% for whole blood and urine samples, respectively. The calibration curve for PCP showed good linearity in the range 2.5–100 ng mL−1 whole blood and 0.5–100 ng mL−1 urine. The detection limits were approximately 1.0 ng mL−1 for whole blood and 0.25 ng mL−1 for urine.
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  • 57
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    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 19 (1996), S. 403-408 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Cryogenic trapping ; Capillary ; Focusing ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cryogenic trapping of solutes leads to narrowing of the chromatographic band. By placing the trap at the end of a capillary column, it is possible to study the effectiveness of the trap in terms of producing a sharpened elution profile. The trap may be heated by supplementary heating, but here convective heating from the GC oven is employed simply by turning off the cryogenic coolant. It is estimated that it takes about 50 s for the trap to heat up sufficiently to allow trapped solute to be remobilized, although this depends upon the oven temperature and thermal mass of the trap. It can also be shown that the more volatile solutes mobilize faster from the trap in this particular mode of operation. The recovery of trapped components shows that there is essentially quantitative trapping, and the solutes are trapped just at the leading edge of the trap.
    Additional Material: 4 Ill.
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  • 58
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    Journal of High Resolution Chromatography 19 (1996), S. 277-283 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Coupled columns ; Four factor optimization ; Simplex method ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Optimization of a gas chromatographic system with two capillary columns coupled in series in a single oven for the linear temperature programmed separation of a mixture of C1—C10 hydrocarbons has been carried out using the simplex optimization method. The following four selectivity parameters were optimized: the initial temperature of the oven; the initial hold time; the temperature programmed rate; and the pressure at the mid-point of the system. The optimization procedure was monitored by the Cp criterion.
    Additional Material: 3 Ill.
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  • 59
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    Journal of High Resolution Chromatography 19 (1996), S. 359-361 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Atomic emission detection ; Triclosan ; Dental plaque ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A validated gas chromatographic method for the determination of triclosan in human dental plaque is described. Based on plaque sample weights of 10 mg, the limit of detection (2 × S/N) is 0.5 μg/g. The method is linear (r = 0.9986) from the limit of detection to 50 μg/g. Recoveries from placebos spiked with 2.0, 25, and 50 μg/g of triclosan were 105.6%±7.5%, 107.2%±3.1%, and 99.1%±1.1%, respectively (n = 3 at each level). Twenty replicate preparations and analyses of a homogenized sample, conducted by two operators over the course of 4 days, showed agreement to within 9% RSD. Analyses of dental plaque collected from patients after brushing with dental cream containing triclosan, shows triclosan to be retained in dental plaque at concentrations above the minimum inhibitory concentration (1 μg/g) after 12 h.
    Additional Material: 1 Ill.
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  • 60
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    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 19 (1996), S. 511-514 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Enantiomer separation ; Amino acids ; N-Alkyloxycarbonyl alkylamide derivatives ; Nucleophilic substitution ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The enantiomers of amino acids were first converted into N-alkyloxycarbonyl 2,2,2-trifluoroethyl esters, and then into N-alkyloxycarbonyl alkylamides by nucleophilic substitution of the ester group with amines. The first reaction proceeds instantaneously, while the second substitution occurs smoothly with n-propylamine and isobutylamine. The final derivatives were produced for separation on a capillary column coated with Chirasil-Val by GC. Pro, which is difficult to separate completely as its N-perfluoroacyl alkyl ester derivative, showed complete separation of the enantiomeric pair. All amino acids examined in this study showed an increased separation factor.
    Additional Material: 3 Ill.
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  • 61
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    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 19 (1996), S. 543-548 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; High temperature ; Dead time ; Constants of the n-alkane retention time curve ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In gas liquid chromatography, the column dead time and the constants of the n-alkane retention time curve are calculated by the multiparametric least-squares regression iterative method at high temperature between 180 and 270°C. The method was applied to two types of columns. The first group includes eight packed columns (seven OV polymethylphenylsiloxane and Apolane-87), while the second includes five glass capillary columns (four methylsilicone with different film thicknesses and Apolane-87). The calculated tM and b values were compared with those obtained by Guardino's, Grobler's, and Kaiser's methods. The influences of coating thickness and temperature thereon were investigated.
    Additional Material: 4 Tab.
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  • 62
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    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 19 (1996), S. 151-154 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Atomic emission spectroscopy ; Enantiomeric separation ; Cyclodextrins ; Chemical warfare agents ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of the organophosphorus nerve agents sarin, tabun, and cyclohexyl methylphosphonofluoridate (GF) produces a mixture of two stereoisomers except for soman where four stereoisomers are produced. Significant differences exist in the reported toxicity and AChE inhibition rates of the various stereoisomers. This makes the ability to distinguish between the different stereoisomers desirable. Five different derivatized cyclodextrin stationary phases developed for gas chromatography were tested for their ability to resolve the nerve agent stereoisomers using a gas chromatograph interfaced to an atomic emission detector. Of the five columns that we examined, only the 2,6-di-O-pentyl-3-O-trifluoroacetyl or 2,6-di-O-pentyl-3-O-butyryl γ-cyclodextrins were able to successfully resolve all four soman stereoisomers. The elution order for each column was determined using solutions of isolated soman stereoisomers. Enantiomers of sarin, tabun, and GF were resolved with varying degrees of success on the different cyclodextrin stationary phases. Only the butyryl γ-cyclodextrin was able to separate the enantiomers of all four of the nerve agents examined in this study. The capacity (k) and selectivity (α) factors were determined for each of the chemical warfare agents successfully separated. The TNO Prins Maurits Laboratory in the Netherlands has previously developed several different chromatographic methods to resolve the stereoisomers of soman, sarin, and tabun. The advantage of the method described here is that commercially available cyclodextrin gas chromatography columns were used to resolve the stereoisomers, thereby facilitating rapid and routine analysis of organophosphorus nerve agents.
    Additional Material: 3 Ill.
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  • 63
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    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 19 (1996), S. 257-262 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Solid-phase microextraction ; Food analysis ; Wine bouquet ; Monoterpenes ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The extraction, identification, and quantification of wine aroma compounds are preliminary steps required for further investigation of wine quality, i.e. determination of the varieties of grapes used, the production process, and the origin and age of the wine. This paper deals with the optimization of solid-phase microextraction for the determination of compounds which produce wine bouquet. Optimum operating conditions have been determined to obtain high reproducibility at low cost and with low time-consumption. Several factors influencing the equilibrium of the aroma compounds between the sample and the fiber must be taken into account, including length of contact time between the two phases involved, speed of agitation of the sample, the matrix in which the process takes place, and, furthermore, the place, duration, and temperature of desorption in the injector of the chromatograph.
    Additional Material: 8 Ill.
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  • 64
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    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 19 (1996), S. 263-266 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Mass spectrometry ; Purge and trap ; Vegetable oil ; Soya oil ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The analysis of volatile compounds, and particularly of certain hydrocarbons, e.g. pentane, and some aldehydes, e.g. hexanal, has been used to estimate the degree of oxidation of vegetable oil. We have tested a dynamic headspace technique without heating the sample during the purge time of the analysis. Some tests have been performed after heating the sample at 180°C for a specified time before the analysis, to compare the results of analysis with and without heating. The best results were obtained at room temperature.
    Additional Material: 3 Ill.
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  • 65
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    Journal of High Resolution Chromatography 19 (1996), S. 639-642 
    ISSN: 0935-6304
    Keywords: Liquid chromatography ; Gas chromatography ; Airborne particulate matter ; Nitroarenes ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Normal-phase HPLC has been applied to the separation of nitroarenes from dichloromethane extracts from airborne particulate matter samples collected in urban regions of Upper Silesia. GC-MS and capillary gas chromatography with NP detector analysis of the nitroarene fraction made it possible to identify and determine quantitatively those compounds which dominate in the organic matter emitted to the atmosphere in highly industrialized regions (2-nitrofluorene, isomeric nitroarenes of MW = 247, i.e. nitropyrene/nitrofluoranthene/nitroacephenanthrylene).
    Additional Material: 4 Ill.
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  • 66
    ISSN: 0935-6304
    Keywords: Solid-phase extraction-thermal desorption ; Gas chromatography ; Ion trap detection ; Tandem mass spectrometry ; Water samples ; Microcontaminants ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An improved set-up for solid-phase extraction with thermal desorption coupled on-line to gas chromatography (SPETD-GC) is presented. It includes a newly designed liner for a programmable temperature vaporizer (PTV) and an improved water elimination system. The SPETD procedure now includes a washing step with HPLC-grade water to prevent degradation of analytes due to interaction with remaining sample constituents. The system was used to analyze surface and tap water samples over a 4-month period. No decrease of chromatographic or trace-enrichment performance was observed, and a liner packed with Tenax GR could be used for at least 150 analyses. The SPETD module was coupled to GC with ion-trap detection for mass spectrometric (MS) and MS/MS detection. The linearity and repeatability of the procedure for several pesticides which were tested in the 0.5-10 μg/1 range were fully satisfactory (1 μg/1, RSD range 5-11%; n = 5). When using sample volumes of 0.1 ml only, detection limits were as low as 0. 1-0.2 μg/1. As an example, the confirmation and quantification of a suspected pesticide in a real-life sample using electron impact and positive chemical ionization in both the MS and MS/MS mode is shown.
    Additional Material: 7 Ill.
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  • 67
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    Angewandte Chemie International Edition in English 35 (1996), S. 241-270 
    ISSN: 0570-0833
    Keywords: alkenes ; asymmetric syntheses ; Horner-Wittig reactions ; phosphane oxides ; synthetic methods ; Alkenes ; Asymmetric synthesis ; Horner-Wittig reaction ; Phosphane oxides ; Synthetic methods ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In 1959, Horner showed that metalated alkyldiphenylphosphane oxides react with aldehydes or ketones to give alkenes. With this reaction, the diphenylphosphoryl (Ph2PO) group made its entrance into synthetic organic chemistry. In the thirty-six years since that date, extensive research has shown that this olefination, the Horner-Wittig reaction, has unique properties that make it much more than simply the phosphane oxide cousin of the more famous phosphorus-based olefinations - the Wittig reaction (based on phosphonium salts) and the Wadsworth-Emmons reaction (based on phosphonate esters). Early work on the Horner-Wittig reaction concentrated on the reactivity of phosphane oxides and the regioselectivity of their reactions, but more recently the power of the Ph2PO group to control the stereochemistry of alkenes, and to produce “on demand” either stereoisomer in high stereochemical purity, has emerged. From the study of these stereocontrolled Horner-Wittig reactions arose the realization that the Ph2PO group is useful not only for the control of the two-dimensional stereochemistry of alkenes, but also of three-dimensional stereochemistry in general.After a brief introduction to phosphane oxide chemistry, this review will examine the Horner-Wittig reaction, in both its original and “stereocontrolled” varieties. From there, we will move on to an account of the stereoselective construction of molecules containing the Ph2PO group, concentrating on the stereochemical directing effects of the Ph2PO group and on the role of its unique combination of attributes - steric bulk, electronegativity, and Lewis basicity - in controlling these reactions. Finally, we will present what is intended as a practical guide to this chemistry, covering the type of functionalized alkenes that have been made with the help of the Ph2PO group and giving guidelines that we hope will help the organic chemist to make the most of the chemistry the Ph2PO group has to offer.
    Additional Material: 11 Tab.
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  • 68
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    Angewandte Chemie International Edition in English 35 (1996), S. 1050-1066 
    ISSN: 0570-0833
    Keywords: carbon-carbon coupling ; carbon monoxide ; carbonylation ; radicals ; synthetic methods ; C-C coupling ; Carbonylation ; Radicals ; Synthetic methods ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Although known since the 1950s, free-radical carbonylation has not received much attention until only recently. In the last few years the application of modern free-radical techniques has revealed the high synthetic potential of this reaction as a tool for introducing CO into organic molecules. Clearly now is the time for a renaissance of this chemistry. Under standard conditions (tributyltin hydride/CO) primary, secondary, as well as tertiary alkyl bromides and iodides can be efficiently converted into the corresponding aldehydes. Aromatic and α,β-unsaturated aldehydes can also be prepared from the parent aromatic and vinylic iodides. If the reaction is carried out in the presence of alkenes containing an electron-withdrawing substituent, the initially formed acyl radical subsequently adds to the alkene, leading to a general method for the synthesis of unsymmetrical ketones. This three-component coupling reaction can be extended successfully to allyltin-mediated reactions. Thus, β,γ-enones can be prepared from organic halides, CO, and allyltributylstannanes. In a remarkable one-pot procedure alkyl halides can be treated with a mixture of alkene, allyltributylstannane, and carbon monoxide in a four-component coupling reaction that provides β-functionalized δ,∊-unsaturated ketones by the formation of three new C—C bonds. The reaction of 4-pentenyl radicals with CO leads to acyl radical cyclization, which provides a useful method for the synthesis of cyclopentanones. Certain useful one-electron oxidations can be combined efficiently with free-radical carbonylations. These findings and others discussed in this article clearly demonstrate that free-radical carbonylation can now be considered a practical alternative to transition metal mediated carbonylation.
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  • 69
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    Angewandte Chemie International Edition in English 35 (1996), S. 2056-2083 
    ISSN: 0570-0833
    Keywords: protecting groups ; retrosynthetic analyses ; synthetic methods ; total syntheses ; Protecting groups ; Retro reactions ; Synthetic methods ; Total synthesis ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The choice of protecting groups is one of the decisive factors in the successful realization of a complex, demanding synthetic project. The protecting groups used influence the length and efficiency of the synthesis and are often responsible for its success or failure. A wide range of blocking groups are currently available for the different functional groups; however, an overall strategy combining these different masking techniques in an advantageous and reliable manner has never been proposed or at best only for individual cases. This review attempts to make a contribution to filling this gap. First a very short overview of the most commonly used protecting groups will be given, in which they are classified according to their lability and not according to the functional group they protect. This classification clarifies coherent concepts for the development of blocking strategies. On the basis of this brief summary reliable strategies will then be illustrated and developed with selected examples from the recent literature by which protecting groups may be combined successfully and advantageously in synthetic projects of differing degrees of complexity and difficulty.
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  • 70
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    Angewandte Chemie International Edition in English 35 (1996), S. 1380-1419 
    ISSN: 0570-0833
    Keywords: glycals ; glycoconjugates ; glycosylations ; oligosaccharides ; synthetic methods ; Glycals ; Glycoconjugates ; Glycosylation ; Oligosaccharides ; Synthetic methods ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This review provides a personal account of the explorations of a research group in oligosaccharide and glycoconjugate construction. The journey began twenty years ago with the study of Diels-Alder reactions of complex dienes. By extending this methodology to aldehydo-type heterodienophile equivalents, access to unnatural glycals was gained (LACDAC reaction). From this point a broad-ranging investigation of the use of glycals in the synthesis of oligosaccharides and other glycoconjugates was begun. Mobilization of glycals both as glycosyl donors and glycosyl acceptors led to the strategy of glycal assembly. Several new glycosylation techniques were developed to provide practical underpinning for this logic of glycal assembly. Glycal-based paradigms have been shown to be nicely adaptable to solid phase supported synthesis. Moreover, glycal assembly - both in solution and on solid phases - has been used to gain relatively concise and efficient entry to a variety of biologically interesting and potentially valuable constructs. Some of these syntheses, particularly in the field of tumor antigens, have led to novel compounds which are in the final stages of preclinical assessment. This review presents an account of the chemical reasoning at the center of the program.
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  • 71
    ISSN: 0570-0833
    Keywords: computer chemistry ; synthesis planning ; WODCA ; Synthetic methods ; Computer chemistry ; Synthesis design ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The planning of syntheses in organic chemistry has continuously been given more solid foundations during the last decades. Widely applicable rules have been formulated. Nearly parallel with the systematization of this field the potential for the automation of synthesis planning by the use of computers has been promulgated. However, after more than two decades of continuing efforts by a number of groups, computer-assisted synthesis planning, which relies on large libraries of synthons and transforms, has failed to establish itself firmly. This is in marked contrast to the acceptance of reaction databases. Their use has become routine with a surprisingly short time. Apparently the classical approaches to computer-assisted synthesis planning do not satisfy the needs of the preparative chemist. However, this lack of success does not yet mean the complete demise of the whole field. The conceptual shortcomings and problems of the first generation of programs are both of technical and psychological nature and need to be critically analyzed. Meanwhile, work has begun on systems of the second generation, which try to support the chemist in the synthesis laboratory with new methods in novel ways. Care is taken to mimic and support the typical planning style of the human chemist, who often on the spur of the moment switches direction in planning as well as his (sub) goals and methods. New tools that correspond better to the thinking patterns and working habits of chemists empower the user to plan syntheses of organic molecules in an interactive and innovative fashion. We feel that this field is far from dead and continue our research activities. In this article we introduce a system with a number of novel concepts and demonstrate its capabilities with some practical examples.
    Additional Material: 19 Ill.
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  • 72
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    Angewandte Chemie International Edition in English 2 (1963), S. 515-523 
    ISSN: 0570-0833
    Keywords: Permethylation ; Carbohydrates ; Methylation ; Gas chromatography ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Methylation of mono-, oligo-, and polysaccharides with methyl iodide/barium oxide or dimethyl sulfate/barium hydroxide in dimethyl sulfoxide as solvent rapidly leads to high degrees of methylation. Depending on the structure and solubility of the substrate, permethylation can be achieved either in one operation or by repetition of the same treatment. Procedures of permethylation of various carbohydrates are given. The methyl glycosides obtained on methanolysis can be separated and determined quantitatively by gas chromatography. The preparation of separating columns with minimum retention for this purpose is described. Pullulan was shown to have the structure of a completely linear polymer of maltotriose units connected by α-1→6-linkages. - In addition the gaschromatographic identification of methyl ethers of glucosamine and galactosamine is reported.
    Additional Material: 15 Ill.
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  • 73
    ISSN: 0570-0833
    Keywords: Radiocarbon ; Gas chromatography ; Trace analysis ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In biochemical work with isotopic tracers, it is frequently advantageous to investigate samples in the gas phase. In this way, the selectivity of gas-chromatographic separating columns and the sensitivity of detectors can be utilized for both the detection of gas-chromatographic fractions and the determination of their radioactive portions. Conversion of materials separated by gas chromatography into a single standard chemical compound prior to measurement of the radioactivity is recommended. Methods suitable for 14C-labelled compounds can also be applied to those labelled with 3H or 35S.
    Additional Material: 8 Ill.
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  • 74
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    Angewandte Chemie International Edition in English 2 (1963), S. 24-29 
    ISSN: 0570-0833
    Keywords: 3-Aminoquinazol-4-one ; 3-Aminobenzotriazin-4-one ; Quinazolones ; Benzotriazinones ; Synthetic methods ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Among the derivatives of 3-aminoquinazol-4-one and 3-aminobenzotriazin-4-one are compounds with narcotic, sedative, analgetic, and muscle-relaxant properties. Of special interest are compounds with one or several urethane groups and those substituted in the 3-position by a morpholine moiety.
    Additional Material: 4 Tab.
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  • 75
    ISSN: 0570-0833
    Keywords: Racemization ; Peptide synthesis ; Gas chromatography ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: It is shown that the methyl esters of many diastereoisomeric N-trifluoroacetyldipeptides can be separated by gas chromatography on Golay columns. This makes it possible for the first time to carry out accurate quantitative investigations of recemization occurring during peptide synthesis without resort to measurements of optical rotation or enzymatic cleavage, and witout having to isolate the peptides. Some well-known methods of forming peptides were examined using the synthesis of the methyl ester of carbobenzoxy-L-valyl-L-valine as an example. The synthesis of the methyl ester of N-trifluoroacetyl-L-valyl-L-valine was investigated as a model for the linking of peptides. The influence on racemization of numerous factors was determined. General conclusions could be drawn regarding peptide synthesis.
    Additional Material: 3 Ill.
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  • 76
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    Angewandte Chemie International Edition in English 2 (1963), S. 225-238 
    ISSN: 0570-0833
    Keywords: Pyridinium salts ; Synthetic methods ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This review discusses syntheses leading to a new type of N-vinylpyridinium salts, to novel anionocyanines, to aminophenazines and alloxazines, as well as to (aza-) dehydroquinolizinium, acridizinium, and morphanthridizinium salts. In addition, Mannich reactions and aminoalkylations at active methylene groups of cycloimmonium salts, and their reactions with amines are treated. The possibilities offered by the “Ortoleva-King” reaction are demonstrated using numerous examples, such as a new route leading to the yohimbine skeleton.
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  • 77
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    Angewandte Chemie International Edition in English 2 (1963), S. 309-323 
    ISSN: 0570-0833
    Keywords: s-Triazines ; Synthetic methods ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The preparation and properties of s-triazine are discussed. Nucleophilic reagents (even water) readily attack s-triazine. Thus, open-chain and heterocyclic compounds, e.g. formamidines, aminomethylene compounds, and triazole, pyridine, and pyrimidine deravatives are accessible from s-triazine. With amidines and imido ethers substituted triazines are obtained (by trans-triazination).The latter are formed via open-chain intermediates.
    Additional Material: 11 Tab.
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  • 78
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    Angewandte Chemie International Edition in English 2 (1963), S. 380-393 
    ISSN: 0570-0833
    Keywords: Pyridinium salts ; Synthetic methods ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cleavage of N-phenylpyridinium or N-vinylpyridinium salts with secondary aliphatic amines leads to aromatic amino compounds or enamines which are often unobtainable by other routes. The other fragment, glutacondialdehyde or its monoanil, gives azulenes, as shown by Ziegler and Hafner, as well as König; these compounds can also be prepared from alkylpyridinium salts with cyclopentadienylsodium (Hafner). Syntheses of labile aldehydes which are otherwise difficult to obtain and of α-ketocarboxylic acids, starting from pyridinium salts and proceeding via nitrones or α-cyanoanils, are illustrated by many new examples. Benzimidazoles, benzothiazoles, and amidines are accessible from pyridinium salts via nitrones or α-cyanoanils; cyanoanils can be transformed into quinoxalines (including xanthopterine), perimidines, etc. Furthermore, nitrosonaphthols and nitrosonaphthylamines react with pyridinium salts containing an active methylene group on the nitrogen, leading to new ring systems. Further synthetic possibilities arise from nucleophilic displacements of the pyridine in pyridinium salts by SN 2 reactions. Combination of the route via nitrones with the methods of Arndt-Eistert, Ortoleva-King, or with chloromethylation constitutes a significant enlargement of its range of application. The formation of α-cyanoanils from diazoketones permits synthesis of α-keto-β-amino acids from α-amino acids, or of phenylglyoxylic acids from benzoic acids by chain extension.
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