R. Kallenborn's Chiral environmental pollutants : trace analysis and PDF

By R. Kallenborn

ISBN-10: 3540664238

ISBN-13: 9783540664239

ISBN-10: 3642085695

ISBN-13: 9783642085697

This monograph incorporates a survey at the position of chirality in ecotoxicological procedures. the point of interest is on environmental hint research. parts reminiscent of toxicology, ecotoxicology, artificial chemistry, biology, and physics also are coated intimately in an effort to clarify different homes of enantiomers in environmental samples. This monograph grants a entire survey for environmental hint analysts, analytical chemists, ecotoxicologists, nutrients scientists and skilled lab employees.

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Extra info for Chiral environmental pollutants : trace analysis and ecotoxicology

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J Chromatogr 254:282-284 113. Oi N, Doi T, Kitahara H, Inda Y (1981) Direct separation of some alcohol enantiomers by gas chromatography with amino acid derivatives as chiral stationary phases. J Chromatogr 208:404-408 114. Frank H, Nicholson GJ, Bayer E (1977) Rapid gas chromatographic separation of amino acid enantiomers with a novel chiral stationary phase. J Chromatogr Sci 15:174-176 115. Frank H, Nicholson GJ, Bayer E (1978) Chirale Polysiloxane zur Trennung von optischen Antipoden. Angew Chern 90:396-398; Angew Chern Int Ed Eng117:363 116.

2; [69]) and in cod liver oil (see Sect. 1; [26]). Garrison et al. were mainly interested in o,p'- and p,p'-DDT degradation by plant enzymes as a potential phytoremediation process. Their experimental approach is based on the observation that several plant enzymes can degrade organic pollutants [68]. These include, for example, nitroreductases that reduce nitro moieties to amines and dehalogenases that replace halogen with hydrogen. For instance, aliphatic halocarbons such as hexachloroethane and carbon tetrachloride are readily reduced to compounds with a lower degree of halogenation by dehalogenase enzymes that occur in a variety of plants.

Krebs H, Rasche R (1954) Uber die chromatographische Spaltung von Racematen I. Optisch aktive Kobaltkomplexe von Dithiosiiuren. Z Anorg Chern 276:236-238 24. Krebs H, Schumacher W (1966) Uber die chromatographische Spaltung von Racematen. IV. Camphersiiuren, Diphensiiuren und Aminosiiuren. Chern Ber 99:1341-1346 25. Steckelberg W, Bloch M, Musso HJ (1968) Notiz zur Antipodentrennung von Biphenylderivaten durch Chromatographie. Chern Ber 101:1519-1521 26. Taylor LT, Busch DH (1967) Chromatographic resolution of the antipodes of a helical complex of nickel(II).

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Chiral environmental pollutants : trace analysis and ecotoxicology by R. Kallenborn

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