Synthesis of n-isomers: Native and deuterium-labelled short-chain perfluoroalkane sulfonamide derivatives

IF 1.7 4区 化学 Q3 CHEMISTRY, INORGANIC & NUCLEAR
D. Jérémy Liwara , Anton Pavlov , Craig Mckenzie , Jon E. Johansen , Pim E.G. Leonards , Sicco Brandsma , Jacob de Boer , Huiling Liu
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引用次数: 0

Abstract

Perfluorooctane sulfonamide derivatives have been extensively used by industry for their surfactant properties and as building blocks for other perfluoroalkyl substances (PFAS). Due to their environmental impact and their potential degradation to other harmful PFAS, short-chain sulfonamide derivatives alternatives were introduced. However, these are now also suspected to be present in different environmental matrices and there is a lack of labelled and unlabelled reference standards to perform analyses. To address this gap, 40 native and deuterium labelled short-chain perfluoroalkane sulfonamide derivatives were synthesized, utilizing commercial perfluoroalkane sulfonyl fluoride as starting materials. All products were synthesized and then purified to obtain linear n-isomer reference standards. NMR, GC-FID-MS and LC-MS techniques were used for product identification and purity assessment. Recrystallization method was developed to selectively isolate the n-isomer from the isomer mixtures, thereby providing valuable reference and internal standards for environmental and toxicological investigations.

Abstract Image

正异构体的合成:原生和氘标记短链全氟烷磺酰胺衍生物
全氟辛烷磺酰胺衍生物因其表面活性剂特性以及作为其他全氟烷基物质(PFAS)的基础成分而被工业界广泛使用。由于其对环境的影响及其降解为其他有害全氟烷基物质的可能性,人们开始使用短链磺酰胺衍生物替代品。然而,这些物质目前也被怀疑存在于不同的环境基质中,而且缺乏标记和未标记的参考标准来进行分析。为了填补这一空白,研究人员利用商用全氟烷基磺酰氟作为起始材料,合成了 40 种原生和氘标记的短链全氟烷磺酰胺衍生物。所有产品在合成后都进行了纯化,以获得线性正异构体参考标准。采用 NMR、GC-FID-MS 和 LC-MS 技术对产品进行鉴定和纯度评估。开发的重结晶方法可从异构体混合物中选择性地分离出 n-异构体,从而为环境和毒理学研究提供有价值的参考标准和内部标准。
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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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