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31.
For decades, toxaphene had been used as a major chloropesticide. Degradation of the multicomponent mixture in the environment was mainly reported to be due to anaerobic dechlorination and hydrodechlorination. Little was known about oxidative transformation processes and the potential hydroxylated metabolites were not available as standard compounds. For this reason we synthesized hydroxylated polychlorobornanes by the UV-induced photochlorination of 2-endo-bornyl acetate with sulfuryl chloride followed by hydrolysis of the acetate moiety. The released polychlorinated 2-endo-hydroxybornanes were slightly higher chlorinated the longer the reaction was maintained. After 8 h, the main products were pentachlorinated hydroxybornanes followed by hexa- and heptachlorinated homologues. Traces of octachlorinated hydroxybornanes were also observed. The GC/ECNI-MS spectra of the products were characterized by the molecular ions and the [M-Cl]− fragment ions. The molecular ions of the polychlorinated hydroxybornanes are isobaric with those of polychlorinated biphenyls. E.g. hexachlorohydroxybornanes (C10H12Cl6O) and hexachlorobiphenyls (C12H4Cl6) show the molecular ion at m/z 358. Based on fractionation experiments on silica with the synthesis products it might be possible that OH-CTTs if present in samples will elute into a more polar fraction usually discarded or not collected. Both problems might explain why these compounds have not been more frequently described in the scientific literature. 相似文献
32.
Yuxin Lu Xiang Li Cagnetta Giovanni Bo Wang 《Frontiers of Environmental Science & Engineering》2023,17(7):89
33.
A preliminary investigation of the solution phase behaviour of the biomarker compound 1-aminopropan-2-one (APR) using NMR
spectroscopy was carried out. This was achieved, in part, by synthesis of APR with13C-enrichment in the methylene position. In this paper, we report that this biomarker undergoes H/D exchange with D2O, probably via an enol intermediate. In addition, use of13C-enriched APR enabled its detection by13C NMR spectroscopy at environmentally relevant concentrations. 相似文献