基于非靶标分析的新型PFAS的合成、纯化和表征

IF 1.7 4区 化学 Q3 CHEMISTRY, INORGANIC & NUCLEAR
Ana R.L. Araujo , Anton Pavlov , Jon Eigil Johansen , Sicco Brandsma , Huiling Liu
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引用次数: 0

摘要

全氟和多氟烷基物质是最普遍的环境污染物之一。由于这些物质的毒性和广泛使用,必须对其进行管制,以减少相关的危害。有效的监管需要准确测量PFAS浓度,但缺乏商业参考标准阻碍了通过非目标分析技术发现的新型PFAS的鉴定和定量。在这项工作中,我们的目标是根据文献中报道的非靶向分析结果,通过合成新的PFAS参考标准来填补这一空白。我们合成了17个新的PFAS标准品,包括3个氟端粒硫醚氨基磺酸(FTSASs)、3个氟端粒磺酰氨基磺酸(FtSO2AoS)、6:2氟端粒磺酰氨基磺酸(6:2 FtSOAo)、3个全氟烷磺酰胺二乙酸(FASEE二酸)、3个全氟烷基酰胺烷基胺(PFAAAm)、3个全氟(4-甲基-3,6-二草辛烷-7-烯)磺酸钠(PS酸钠盐)、全氟(4-甲基-3,6-二氧辛-7-烯)磺酸(PS酸)、全氟-3-{[1-(乙基氧基)丙烷-2-基]氧}丙烷酸(EVE酸)和6-(2,2,3,3,4,4,4-七氟丁氧基)己烷-1-醇。通过多种化学反应合成该化合物,并选择干柱真空色谱法(DCVC)作为最佳纯化技术。当分支异构体存在时,通过再结晶得到线性异构体产物。采用核磁共振波谱(¹H,¹⁹F,¹³C)和质谱(m/z, LC-MS或GC-MS)相结合的方法确认合成标准品的鉴定和纯度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Synthesis, purification and characterisation of novel PFAS following nontarget analysis

Synthesis, purification and characterisation of novel PFAS following nontarget analysis
PFAS, or per- and polyfluorinated alkyl substances, are among the most prevalent environmental contaminants. Because of their toxicity and widespread use, these substances must be regulated in order to reduce the associated hazards. Effective regulation requires accurate measurement of PFAS concentrations, but the lack of commercially available reference standards hinders the identification and quantification of novel PFAS discovered through nontarget analysis techniques. In this work, we aimed to fill this gap by synthetising new PFAS reference standards, based on findings reported in the literature through nontarget assays.
We performed the synthesis of 17 novel PFAS reference standards, including three fluorotelomer thioether amido sulfonic acid (FTSASs), three fluorotelomer sulfonyl amido sulfonic acid (FtSO2AoS), 6:2 Fluorotelomer sulfinyl amido sulfonic acid (6:2 FtSOAo), three perfluoroalkane sulfonamide diacetic acids (FASEE diacids), three perfluroalkyl amidoalkyl amine (PFAAAm), perfluoro (4-methyl-3,6-dioxaoct-7-ene) sodium sulfonate (PS acid sodium salt), perfluoro (4-methyl-3,6-dioxaoct-7-ene) sulfonic acid (PS acid), perfluoro-3-{ [1-(ethenyloxy)propan-2-yl]oxy}propanoic acid (EVE acid), and 6- (2,2,3,3,4,4,4-Heptafluorobutoxy)hexan-1-ol. Various chemical reactions were carried out to synthesise the chemicals, and the Dry Column Vacuum Chromatography (DCVC) was selected as the best purification technique. The linear isomer product was obtained by recrystallisation when branched isomers were present. The identity and purity of the synthesised reference standards were confirmed using a combination of NMR spectroscopy (¹H, ¹⁹F, ¹³C) and mass spectrometry (m/z, LC-MS, or GC–MS).
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来源期刊
Journal of Fluorine Chemistry
Journal of Fluorine Chemistry 化学-无机化学与核化学
CiteScore
3.80
自引率
10.50%
发文量
99
审稿时长
33 days
期刊介绍: The Journal of Fluorine Chemistry contains reviews, original papers and short communications. The journal covers all aspects of pure and applied research on the chemistry as well as on the applications of fluorine, and of compounds or materials where fluorine exercises significant effects. This can include all chemistry research areas (inorganic, organic, organometallic, macromolecular and physical chemistry) but also includes papers on biological/biochemical related aspects of Fluorine chemistry as well as medicinal, agrochemical and pharmacological research. The Journal of Fluorine Chemistry also publishes environmental and industrial papers dealing with aspects of Fluorine chemistry on energy and material sciences. Preparative and physico-chemical investigations as well as theoretical, structural and mechanistic aspects are covered. The Journal, however, does not accept work of purely routine nature. For reviews and special issues on particular topics of fluorine chemistry or from selected symposia, please contact the Regional Editors for further details.
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