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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 3 (1989), S. 351-353 
    ISSN: 0268-2605
    Keywords: molluscs ; shells ; arsenicals ; antimony ; organotin ; speciation ; methylarsenicals ; butyltin ; mass spectrum ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Inorganic arsenic(III) and arsenic(V), methyl-arsenicals, antimony(III), and antimony(V), and butyltin derivatives are present in the shells of molluscs found in the coastal waters of British Columbia.
    Additional Material: 1 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 6 (1992), S. 207-211 
    ISSN: 0268-2605
    Keywords: Dimethylantimony ; trimethylantimony ; analysis ; hydride generation ; aquatic speciation ; GCAA ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reports in the literature that the compounds MeSb(O)(OH)2 and Me2Sb(O)(OH) are present in marine and fresh-waters need to be re-examined. The results of several synthetic strategies suggest that these methylantimony(V) compounds are either environmentally inaccessible or polymeric in nature. Pure samples of various di- and tri- methylated antimony(V) species were prepared and found to undergo molecular rearrangement reactions when subjected to hydride generation procedures typically used for aquatic speciation.
    Additional Material: 2 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 3 (1989), S. 475-490 
    ISSN: 0268-2605
    Keywords: Arsenic methylation ; arsenic speciation ; methylarsenicals ; sediment ; mine-tailings ; biomethylation ; demethylation ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Laboratory studies have shown that microorganisms present in both natural marine sediments and sediments contaminated with mine-tailings are capable of methylating arsenic under aerobic and anaerobic conditions.Incubation of sediments with culture media produced volatile arsines [including AsH3, (CH3)AsH2, and (CH3)3As] as well as the methylarsenic(V) compounds (CH3)nAs(O) (OH)3-n (n = 1, 2, 3). The concentration of the arsines increased and then decreased in a growth and decay pattern reminiscent of the methylation and demethylation of mercury. Thus, arsenic speciation varied with time, being controlled by the biochemical activity of the dominant microbe(s) at the time of sampling, and changing in response to the ecological succession within the microbial community.The analysis of the interstitial waters of sediments collected from several British Columbia (Canada) coastal sites gave results that were consistent with the culture experiments, in that the methylarsenicals were ubiquitous, but present only in small amounts. It is estimated that methylarsenic(V) species account for less than 1% of the arsenic present in porewaters. The actual proportion was dependent on a number of factors but, contrary to prevailing viewpoints, there was no relationship to the organic content of the sediments, nor did methylation occur only in the presence of high arsenic concentrations. Instead, all of the evidence was consistent with in situ microbial methylation and demethylation processes that are similar to the arsenic transformations that occur in soil ecosystems.The results are discussed in terms of the cycling of arsenic in the marine environment and within the marine food web.
    Additional Material: 8 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 8 (1994), S. 415-422 
    ISSN: 0268-2605
    Keywords: Anaerobe ; arsenic ; microbial ; organoarsenicals ; sediment ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Anaerobic enrichment cultures, isolated from arsenic-contaminated lake sediment in the Canadian sub-arctic and grown in five selective media, methylated arsenate/arsenite to produce mono-, di- and tri-methyl arsenicals. The extent of methylation and methylarsenic species produced varied with the type of enrichment. Iron-reducing, manganese-reducing, sulfate-reducing and broad-spectrum anaerobic heterotrophic mixed cultures all produced methylarsenicals. Sulfate-reducing cultures produced higher concentrations of methylarsenicals (especially trimethyl species) than iron- or maganese-reducers. There is evidence that several of the methylarsenicals, which were hydride-reactive at pH 6, were methylarsenic(III) thiols. The organoarsenicals produced by enrichment cultures were the same as those detected in the porewater of the lake sediments used to initiate the enrichment cultures. Overall, this study demonstrates that microbes from anaerobic lake sediments can methylate (and demethylate) arsenic, a capability shared by manganese-, iron-, and sulfate-reducing microbial consortia.
    Additional Material: 3 Ill.
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  • 5
    ISSN: 0268-2605
    Keywords: Arsenic ; microwave oven digestion ; hydride generation ; atomic absorption spectrometry ; flow injection analysis ; determination ; decomposition ; arsenobetaine ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Environmentally important organoarsenicals such as arsenobetaine, arsenocholine and tetramethylarsonium ion do not form volatile hydrides under the commonly used analytical conditions on treatment with borohydride and it has been difficult to determine their concentrations without further derivatization. This paper describes a rapid method which completely decomposes and oxidizes these arsenicals to arsenate by using potassium persulphate and sodium hydroxide with the aid of microwave energy. The quantitative decomposition of these species permits their determination at low nanogram levels, by hydride generation atomic absorption spectromety (HG AA). A new hydride generator which has high efficiency and minimum dead volume and therefore is suitable for flow injection analysis (FIA) is also described. A system combining flow injection analysis, online microwave oven digestion, and hydride generation followed by atomic absorption measurement, is developed. This system is capable of performing analysis at a sample throughput of 100-120 per hour. Calibration curves were linear from 10 to 200 ng cm-3 of arsenic and the detection limit was 5 ng cm-3 for a 100-μ injection or 0.5 ng of arsenic. All ten organoarsenic compounds studied gave arsenate as the decomposition product, which was confirmed by using molybdenum blue photometric measurement.
    Additional Material: 9 Ill.
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  • 6
    ISSN: 0268-2605
    Keywords: Arsenic ; extracellular ; endocellular ; methylation ; growth medium ; Apiotrichum humicola ; Scopulariopsis brevicaulis ; Candida humicola ; hydride generation-gas chromatography-atomic absorption spectrometry ; trimethylarsine oxide ; methylarsonate ; dimethylarsinate ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The separation and identification of some of the arsenic species produced in cells present in the growth medium when the microorganisms Apiotrichum humicola (previously known as Candida humicola) and Scopulariopsis brevicaulis were grown in the presence of arsenicals were achieved by using hydride generation-gas chromatography-atomic absorption spectrometry methodology (HG GC AA). Arsenite, monomethylarsonate, dimethylarsinate and trimethylarsine oxide were detected following incubation with arsenate. With arsenite as a substrate, the metabolites were monomethylarsonate, dimethylarsinate and trimethylarsine oxide; monomethylarsonate afforded dimethylarsinate and trimethylarsine oxide, and dimethylarsinate afforded trimethylarsine oxide. Trimethylarsine was not detected when the arsenic concentration was 1 ppm.
    Additional Material: 6 Ill.
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  • 7
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 149 (1937), S. 81-84 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 14 (1876), S. 328-346 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 149 (1937), S. 311-316 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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