Absorption properties of körbl-catalyst and manganese dioxide

Summary Körbl-catalyst and manganese dioxide absorb chlorine and bromine quantitatively at room temperature. This property is applied to simultaneous microanalytical determination of carbon, hydrogen and chlorine or bromine in compounds containing carbon, hydrogen, oxygen, chlorine or bromine, but not nitrogen or sulphur.

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Zusammenfassung Der Körbl-Katalysator und Mangandioxid absorbieren Chlor und Brom bei Raumtemperatur quantitativ. Sie wurden daher zur gleichzeitigen Bestimmung von C, H sowie Cl oder Br in Verbindungen verwendet, die C, H, O, Cl (oder Br), nicht aber N oder S enthalten.

     

Design and evaluation of a multi-detection system composed of ultraviolet, evaporative light scattering and inductively coupled plasma mass spectrometry detection for the analysis of pharmaceuticals by liquid chromatography

Reversed-phase liquid chromatography was coupled to a multi-detection system composed of ultraviolet (UV) detection, evaporative laser scattering detection (ELSD) and inductively coupled plasma mass spectrometry (ICP-MS). By applying the principle of post-column solvent compensation, the organic modifier content was kept constant in ELSD and ICP-MS under gradient elution. Chlorine ((35)Cl), bromine ((79)Br and (81)Br) and sulfur ((34)S) were monitored in several pharmaceutical compounds. The limit of quantitation (LOQ) was 80 ng/mL for chlorine (chlorpropamide) and 2 ng/mL for bromine (bromazepam). Calibration graphs were linear from 1.0 microg/mL to 100 microg/mL for chlorpropamide (r(2) 0.990) and from 10 ng/mL to 500 ng/mL for bromazepam (r(2) 0.996). The low LOQ value for bromine allows to quantify bromine in pharmaceutical samples below the 0.05% level of the active pharmaceutical ingredient.     

A Gas Chromatography‐Molecular Rotational Resonance Spectroscopy Based System of Singular Specificity

We designed and demonstrated the unique abilities of the first gas chromatography–molecular rotational resonance spectrometer (GC‐MRR). While broadly and routinely applicable, its capabilities can exceed those of high‐resolution MS and NMR spectroscopy in terms of selectivity, resolution, and compound identification. A series of 24 isotopologues and isotopomers of five organic compounds are separated, identified, and quantified in a single run. Natural isotopic abundances of mixtures of compounds containing chlorine, bromine, and sulfur heteroatoms are easily determined. MRR detection provides the added high specificity for these selective gas‐phase separations. GC‐MRR is shown to be ideal for compound‐specific isotope analysis (CSIA). Different bacterial cultures and groundwater were shown to have contrasting isotopic selectivities for common organic compounds. The ease of such GC‐MRR measurements may initiate a new era in biosynthetic/degradation and geochemical isotopic compound studies.     

Determination of isotope cluster patterns in mass spectra of GC-MS analyses by a chemometric detector

The computer program ISODET recognizes isotope cluster patterns in the mass spectra of the GC-MS analysis of atoms of chlorine, bromine, sulphur and chlorine/bromine combinations. The decision parameters used in the algorithm of the method were calculated by treating 2, 535 mass spectra from the NBS database. The result of the analysis is a graphic output (isotope cluster chromatograms) and tabulated output. The applicability and the reliability of the isotope detector and the mode of using the input program parameters are discussed. The reliability of the correct recognition of isotope clusters evaluated by means of the spectra from the NBS database was 92% for chlorinated and brominated compounds but only 51%, for sulphur containing compounds.     

Assessment of the intramolecular C–H⋯X (X=F,Cl, Br) hydrogen bonding of 1,4-diphenyl-1,2,3-triazoles

The intramolecular six-membered C–H?X (X=F, Cl, Br) hydrogen bonding motif of halogen-substituted 1,4-diphenyl-1,2,3-triazole compounds has been assessed. Twelve triazole derivatives have been designed and prepared, which bear fluorine, chlorine or bromine atoms on the ortho- and/or para-positions of the benzene rings. ¹H NMR, X-ray crystallography, and DFT calculation investigations revealed that the ortho-fluorine, chlorine, and bromine atoms of the benzene ring on the C-4 of the triazole unit all can form six-membered C–H?X hydrogen bonding. In contrast, only fluorine forms similar, relatively stable intramolecular hydrogen bonding on the N-1 side of the triazole unit.     

Sulphur tracer experiments in laboratory animals using 34S-labelled yeast

We have evaluated the use of ³⁴S-labelled yeast to perform sulphur metabolic tracer experiments in laboratory animals. The proof of principle work included the selection of the culture conditions for the preparation of sulphur labelled yeast, the study of the suitability of this labelled yeast as sulphur source for tracer studies using in vitro gastrointestinal digestion and the administration of the ³⁴S-labelled yeast to laboratory animals to follow the fate and distribution of ³⁴S in the organism. For in vitro gastrointestinal digestion, the combination of sodium dodecyl sulphate-polyacrylamide gel electrophoresis and high-performance liquid chromatography and inductively coupled plasma mass spectrometry (HPLC-ICP-MS) showed that labelled methionine, cysteine and other low molecular weight sulphur-containing biomolecules were the major components in the digested extracts of the labelled yeast. Next, in vivo kinetic experiments were performed in healthy Wistar rats after the oral administration of ³⁴S-labelled yeast. The isotopic composition of total sulphur in tissues, urine and faeces was measured by double-focusing inductively coupled plasma mass spectrometry after microwave digestion. It was observed that measurable isotopic enrichments were detected in all samples. Finally, initial investigations on sulphur isotopic composition of serum and urine samples by HPLC-ICP-MS have been carried out. For serum samples, no conclusive data were obtained. Interestingly, chromatographic analysis of urine samples showed differential isotope enrichment for several sulphur-containing biomolecules.     

Simultaneous determination of microgram amounts of chlorine or bromine or iodine and sulfur in organic compounds

A general method for the simultaneous and rapid determination of microgram amounts of chlorine or bromine or iodine and sulfur in organic compounds is described.The procedure is based on the combustion of the sample, containing approximately 0.005 meq of Cl or Br or I and 0.005 meq of S. by the Schöniger flask technique, using potassium hydroxide and hydrazine hydrate as absorption solution. The excess of hydrazine is eliminated with hydrogen peroxide after combustion.This method allows complete reduction of halogens to halides and oxidation of sulfur to sulfate.The halide ions are titrated with mercuric perchlorate and diphenylcarbazone as indicator; the sulfate ions with barium perchlorate and dimethylsulfonazo(III) as indicator.The results obtained are in good agreement with calculated values.     

Environmental analysis of chlorinated and brominated polycyclic aromatic hydrocarbons by comprehensive two-dimensional gas chromatography coupled to high-resolution time-of-flight mass spectrometry

A method for the analysis of chlorinated and brominated polycyclic aromatic hydrocarbon (Cl-/Br-PAHs) congeners in environmental samples, such as a soil extract, by comprehensive two-dimensional gas chromatography coupled to a high resolution time-of-flight mass spectrometry (GC×GC-HRTOF-MS) is described. The GC×GC-HRTOF-MS method allowed highly selective group type analysis in the two-dimensional (2D) mass chromatograms with a very narrow mass window (e.g. 0.02Da), accurate mass measurements for the full mass range (m/z 35-600) in GC×GC mode, and the calculation of the elemental composition for the detected Cl-/Br-PAH congeners in the real-world sample. Thirty Cl-/Br-PAHs including higher chlorinated 10 PAHs (e.g. penta, hexa and hepta substitution) and ClBr-PAHs (without analytical standards) were identified with high probability in the soil extract. To our knowledge, highly chlorinated PAHs, such as C(14)H(3)Cl(7) and C(16)H(3)Cl(7), and ClBr-PAHs, such as C(14)H(7)Cl(2)Br and C(16)H(8)ClBr, were found in the environmental samples for the first time. Other organohalogen compounds; e.g. polychlorinated biphenyls (PCBs), polychlorinated naphthalenes (PCNs), and polychlorinated dibenzofurans (PCDFs) were also detected. This technique provides exhaustive analysis and powerful identification for the unknown and unconfirmed Cl-/Br-PAH congeners in environmental samples.     

Highly chemoselective hydrogenolysis of iodoarenes

The catalytic hydrodehalogenation reaction using molecular hydrogen and Pd/C has been revisited. It is shown that the speed of removal of halogen increases with increasing electronegativity I < Br < Cl. Nevertheless, selective dehydrohalogenation in compounds containing other reducible functions can be achieved only with iodine and not with bromine or chlorine. Selective deiodination of iodobenzophenone could be accomplished without reducing the carbonyl group. Hydrogenolysis of azidoiodoaromatic compounds to the corresponding azido compounds is high yielding. This selectivity was exploited for the labeling of benzophenone- and azido-containing compounds by deuterium and tritium.     

Iodometric microdetermination of chlorine and bromine in some highly halogenated organic compounds

Summary Highly halogenated organic compounds are combusted in a oxygen flask using water as absorbant in the case of chlorine and 0.05% hydrogen peroxide in the case of bromine. The halogenide ion formed is determined by an iodometric procedure. Results showed an average error of ± 0.1% for Cl and ± 0.2% for Br. They are in close agreement with those obtained by a mercurimetric titration. The iodometric titration is to be preferred because of simplicity and rapidity

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Jodometrische Mikrobestimmung von Chlor und Brom in einigen hochhalogenisierten organischen Verbindungen

Zusammenfassung Die Verbindung wird im Sauerstoffkolben verbrannt, wobei Wasser (Cl) bzw. 0,05%ige Wasserstoffperoxidlösung (Br) als Absorptionsmittel verwendet werden. Die gebildeten Halogenide werden jodometrisch bestimmt. Der durchschnittliche Fehler beträgt ± 0,1% (Cl) bzw. ± 0,2% (Br). Die Ergebnisse stimmen gut mit mercurimetrisch erhaltenen überein. Die jodometrische Titration ist wegen der einfachen und schnellen Durchführbarkeit vorzuziehen.

     

Simultaneous microdetermination of carbon,hydrogen, mercury,chlorine, bromine and sulphur in organic compounds

A simple, reliable method for the simultaneous microdetermination of carbon, hydrogen, mercury, chlorine (or bromine) and sulphur in organic compounds is described. The intermediate storage technique is used. Sulphur and the halogens are absorbed on electrolytic silver and determined gravimetrically or titrimetrically. Mercury is absorbed on gold wire, and is weighed as the metal or desorbed and determined by a mercury-8-hydroxy-quinoline method.     

Multivariate data analysis of some Finnish water courses

Summary The following parameters were analyzed 2 to 4 times a year from 37 sampling sites; T, O₂, O₂%, Turbidity, Suspended solids, Conductivity, Alkalinity, pH, Color, COD_Mn, Total nitrogen, Total phosphorus, Cl, Fe, Mn, Total sulphur, K, Na, Ca, Mg, SiO₂, Total organic chlorine and Total organic bromine. Samples were taken from waters loaded by chemical pulp mills, other industries, municipal waste waters and agriculture. Also waters under natural conditions were included. Water samples have been collected and analyzed in co-operation with the National Board of Waters and the Environment. The data set was analyzed by Principal Component Analysis (PCA) to determine correlations between variables, especially between Total organic chlorine and Total organic bromine and others. Typically Total organic chlorine and Total organic bromine correlated with Na, Cl and Total sulphur. It is interesting to note that Total organic chlorine and Total organic bromine did not follow each other in all components. Total organic chlorine was predicted using other variables and Partial Least Squares (PLS) method. Very satisfactory correlation was obtained between analyzed and predicted lgTOCl values. Optimally three different object classes were found from the whole data using fuzzy clustering analysis. One class represents waters in a natural condition, one water loaded mainly by agriculture and one represent the rest of the waters.     

A Gas Chromatography-Molecular Rotational Resonance Spectroscopy Based System of Singular Specificity

We designed and demonstrated the unique abilities of the first gas chromatography–molecular rotational resonance spectrometer (GC-MRR). While broadly and routinely applicable, its capabilities can exceed those of high-resolution MS and NMR spectroscopy in terms of selectivity, resolution, and compound identification. A series of 24 isotopologues and isotopomers of five organic compounds are separated, identified, and quantified in a single run. Natural isotopic abundances of mixtures of compounds containing chlorine, bromine, and sulfur heteroatoms are easily determined. MRR detection provides the added high specificity for these selective gas-phase separations. GC-MRR is shown to be ideal for compound-specific isotope analysis (CSIA). Different bacterial cultures and groundwater were shown to have contrasting isotopic selectivities for common organic compounds. The ease of such GC-MRR measurements may initiate a new era in biosynthetic/degradation and geochemical isotopic compound studies.     

Compound-specific 81Br/79Br analysis by capillary gas chromatography/multicollector inductively coupled plasma mass spectrometry

Brominated organic compounds (BOCs) are of great interest in atmospheric chemistry, natural products, geochemistry, and marine chemistry. The Br isotope ratios ((81)Br and (79)Br; average (81)Br/(79)Br = 0.97277) have significant potential for the study of the source, transport, and fate of these compounds. Currently, there is no published method for determining the Br isotopic content of BOCs in complex mixtures. To measure the ratios of stable Br in BOCs on a compound-specific basis, we assembled a gas chromatography/multicollector inductively coupled plasma mass spectrometry (GC/MCICPMS) system. Background signals, the formation of Ar dimers from organic hydrogen, and the solvent peak did not affect the results. The analysis of three brominated benzenes revealed that 0.3 per thousand precision can be attained when 0.3 nmol of Br are injected. For samples larger than 0.3 nmol Br, the isotopic precision was within a factor of 3 of the shot-noise limit, which is the best possible statistical precision attainable avoiding all other sources of noise.     

Discovering metabolites of post-harvest fungicides in citrus with liquid chromatography/time-of-flight mass spectrometry and ion trap tandem mass spectrometry

In this study, we benefit from the combination of liquid chromatography (LC)/time-of-flight (TOF) MS accurate mass measurements to generate elemental compositions of ions and LC/ion trap multiple MS (MSn) providing complementary structural information, which is useful for the elucidation of unknown organic compounds at trace levels in complex food extracts. We have applied this approach to investigate different citrus fruits extracts, and we have identified two post-harvest fungicides (imazalil and prochloraz), the main degradation product of imazalil ([M + H]+, m/z 257) and a non-previously reported prochloraz degradation product ([M + H]+, m/z 282). The database-mediated identification of the parent compounds was based on the generated elemental composition obtained from accurate mass measurements and additional qualitative information from the high resolution chlorine isotopic clusters of both the protonated molecules (imazalil, [M + H]+ 297.0556, <0.1 ppm error, 2-Cl; prochloraz, [M + H]+ 376.0381, 1.9 ppm error, 3-Cl) and their characteristic fragments ions (imazalil: m/z 255 and 159; prochloraz: m/z 308 and 266). The correlation between the structural information provided by ion trap MS/MS fragmentation pathways of the parent species and the TOF accurate mass elemental composition data of the degradation products were the key to elucidate the structures of the degradation products of both post-harvest fungicides. Finally, where standards were not available (prochloraz), further confirmation was obtained by synthesizing the proposed degradation product by acid hydrolysis of the parent standard and confirmation by LC/TOF-MS.     

中国典型超高硫煤有机相中分子氯存在的实验证据

运用,主性能静态二次离子质谱从中国贵州六枝超高硫无烟煤有机相中观测到分子氯（Cl2）的团簇负离子,从而首次获得分子氯在原煤中存在的实验证据。结合不久前从相同原煤有机相观测到元素硫（S8）的研究结果,表明易挥发性元素能够以其化学单质状态在原煤有机相中稳定存在;其来源可能与地球排气作用与原煤的富含纳米孔隙性质和化学还原微环境密切相关。     

High-temperature experimental and theoretical study of magnetic interactions in diamond and pseudo-diamond frameworks built up from hexanuclear tantalum clusters

Magnetic interactions in solid‐state tantalum cluster compounds have been evidenced by using magnetic susceptibility measurements and corroborated by broken‐symmetry DFT calculations. The three selected compounds are based on [Ta₆X₁₂(H₂O)₆]³⁺ (X=Cl or/and Br) units with edge‐bridged Ta₆ octahedral clusters. Although two of them crystallise in the tetragonal space group I4₁/a, all compounds exhibit a similar arrangement of paramagnetic clusters related to the diamond structural framework (Fd$\bar 3Magnetic interactions in solid-state tantalum cluster compounds have been evidenced by using magnetic susceptibility measurements and corroborated by broken-symmetry DFT calculations. The three selected compounds are based on [Ta(6)X(12)(H(2)O)(6)](3+) (X=Cl or/and Br) units with edge-bridged Ta(6) octahedral clusters. Although two of them crystallise in the tetragonal space group I4(1)/a, all compounds exhibit a similar arrangement of paramagnetic clusters related to the diamond structural framework (Fd ?3m space group). Magnetic parameters were fitted by using the [5,4] Padé approximant of high-temperature series expansion of susceptibility for the Heisenberg model (S=1/2) in the diamond framework, assuming only nearest-neighbouring interactions. Such a model appropriately describes magnetic-susceptibility measurements at temperatures T>0.7|J|/k. The magnetic interaction parameter J between two [Ta(6)Cl(12)(H(2)O)(6)](3+) clusters is estimated to be -64.28(7) cm(-1) ; it has been enhanced by replacing several chlorine inner ligands with bromine ones (J=-123(3) cm(-1) for two [Ta(6)Br(7.7(1))Cl(4.3(1))(H(2)O)(6)](3+) clusters) and is strongest between two bromine [Ta(6)Br(12)(H(2)O)(6)](3+) clusters with a value of -155(1) cm(-1) . Broken-symmetry DFT calculations within spin-dimer analysis confirmed this trend. Those interactions can be explained on the basis of the overlap between singly occupied a(2u) orbitals localised on neighbouring clusters.     

Reference values in blood from inhabitants of Brazil: Br,Cl, K and Na determination using NAA

In this study, bromine (Br), chlorine (Cl), potassium (K) and sodium (Na) were measured in the blood of Brazilian inhabitants from Southeast (S) and Northeast (N) regions. A reference range was established as a function of sex and considering lifestyle factors (non-smokers and non- drinkers). For both regions lower values of K were found in females when compared to males and lower values of Na were found in males compared to females. Increasing trends for Na and Br were observed in the Northeast region.     

A multi-element analyser with a small mass spectrometer as detector

Summary An instrument for the simultaneous determination of up to eight elements in organic material is described. A few milligrams of the sample are rapidly burnt in a stream of oxygen with platinum gauze serving as a catalyst. A small fraction of the combustion gases is directly fed into a simple quadrupole mass spectrometer which, by rapid scanning, monitors twelvem/e values of interest. With the aid of a multiplexer the signals are individually integrated and the results are directly printed in percentages. The whole procedure takes about 2 min. The method has been successfully applied to samples containing the elements carbon, hydrogen, nitrogen, sulphur, fluorine, chlorine, bromine and iodine. The relative precision is in the order of a few percent.

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Multielement-Analysator mit kleinem Massenspektrometer als Detektor

Zusammenfassung Ein Gerät zur gleichzeitigen Bestimmung von bis 8 Elementen in organischen Substanzen wird beschrieben. Einige Milligramm werden schnell in einem Sauerstoffstrom mit Pt-Gaze als Katalysator verbrannt. Ein kleiner Teil der Verbrennungsgase wird direkt in ein einfaches Quadrupol-Massenspektrometer eingegeben, das 12 interessierendem/e-Werte erfaßt. Mit einem Multiplexer werden die Signale einzeln integriert und die Ergebnisse direkt in Prozent ausgedruckt. Die gesamte Operation erfordert 2 min. Das Verfahren wurde erfolgreich für Proben mit Gehalten an C, H, N, S, F, Cl, Br und J angewandt. Die relative Genauigkeit liegt in der Größenordnung einiger Prozente.

Lecture presented at Euroanalysis I Conference, 28. 8.–1. 9. 1972 in Heidelberg, Germany.     

Determination of (34)S:(32)S ratios by FTIR spectroscopy

A new method for determining (34)S:(32)S ratios using Fourier transform infrared spectroscopy has been developed. The four sulphur-containing gases SCO, H(2)S, SF(6) and SO(2) are assessed as possible compounds for the spectroscopic measurements, from which, after a consideration of available lines showing a clear isotopic shift and also of possible synthetic routes to the gas starting from a range of natural sample types, SO(2) was selected for further development of the instrumental method for the isotopic ratio determination. Sulphur in the samples present as the element, as metal sulphides or as organosulphur compounds, is converted by heating with V(2)O(5) into gaseous SO(2), and a part of the 518 cm(-1) band is recorded in the absorbance mode. The optimisation of instrumental parameters and of the chemical reaction conditions is described, and the results from the application of the method to the measurement of the level of enrichment of (34)S in a soil fungus are presented. The agreement between results at the natural abundances of 4.2% was better than 0.04% absolute for a sample size of 1.5 mg of sulphur.